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2020-10-26 19:46:20, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001245002            8063 bp    mRNA    linear   PRI 01-MAY-2013
DEFINITION  Homo sapiens nuclear factor I/C (CCAAT-binding transcription
            factor) (NFIC), transcript variant 1, mRNA.
ACCESSION   NM_001245002
VERSION     NM_001245002.1  GI:350529395
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 8063)
  AUTHORS   Duval,C., Gaudreault,M., Vigneault,F., Touzel-Deschenes,L.,
            Rochette,P.J., Masson-Gadais,B., Germain,L. and Guerin,S.L.
  TITLE     Rescue of the transcription factors Sp1 and NFI in human skin
            keratinocytes through a feeder-layer-dependent suppression of the
            proteasome activity
  JOURNAL   J. Mol. Biol. 418 (5), 281-299 (2012)
   PUBMED   22420942
  REMARK    GeneRIF: the influence of i3T3 on the expression and DNA binding of
            NFI, another TF important for cell proliferation and cell cycle
            progression
REFERENCE   2  (bases 1 to 8063)
  AUTHORS   Lango Allen,H., Estrada,K., Lettre,G., Berndt,S.I., Weedon,M.N.,
            Rivadeneira,F., Willer,C.J., Jackson,A.U., Vedantam,S.,
            Raychaudhuri,S., Ferreira,T., Wood,A.R., Weyant,R.J., Segre,A.V.,
            Speliotes,E.K., Wheeler,E., Soranzo,N., Park,J.H., Yang,J.,
            Gudbjartsson,D., Heard-Costa,N.L., Randall,J.C., Qi,L., Vernon
            Smith,A., Magi,R., Pastinen,T., Liang,L., Heid,I.M., Luan,J.,
            Thorleifsson,G., Winkler,T.W., Goddard,M.E., Sin Lo,K., Palmer,C.,
            Workalemahu,T., Aulchenko,Y.S., Johansson,A., Zillikens,M.C.,
            Feitosa,M.F., Esko,T., Johnson,T., Ketkar,S., Kraft,P., Mangino,M.,
            Prokopenko,I., Absher,D., Albrecht,E., Ernst,F., Glazer,N.L.,
            Hayward,C., Hottenga,J.J., Jacobs,K.B., Knowles,J.W., Kutalik,Z.,
            Monda,K.L., Polasek,O., Preuss,M., Rayner,N.W., Robertson,N.R.,
            Steinthorsdottir,V., Tyrer,J.P., Voight,B.F., Wiklund,F., Xu,J.,
            Zhao,J.H., Nyholt,D.R., Pellikka,N., Perola,M., Perry,J.R.,
            Surakka,I., Tammesoo,M.L., Altmaier,E.L., Amin,N., Aspelund,T.,
            Bhangale,T., Boucher,G., Chasman,D.I., Chen,C., Coin,L.,
            Cooper,M.N., Dixon,A.L., Gibson,Q., Grundberg,E., Hao,K., Juhani
            Junttila,M., Kaplan,L.M., Kettunen,J., Konig,I.R., Kwan,T.,
            Lawrence,R.W., Levinson,D.F., Lorentzon,M., McKnight,B.,
            Morris,A.P., Muller,M., Suh Ngwa,J., Purcell,S., Rafelt,S.,
            Salem,R.M., Salvi,E., Sanna,S., Shi,J., Sovio,U., Thompson,J.R.,
            Turchin,M.C., Vandenput,L., Verlaan,D.J., Vitart,V., White,C.C.,
            Ziegler,A., Almgren,P., Balmforth,A.J., Campbell,H., Citterio,L.,
            De Grandi,A., Dominiczak,A., Duan,J., Elliott,P., Elosua,R.,
            Eriksson,J.G., Freimer,N.B., Geus,E.J., Glorioso,N., Haiqing,S.,
            Hartikainen,A.L., Havulinna,A.S., Hicks,A.A., Hui,J., Igl,W.,
            Illig,T., Jula,A., Kajantie,E., Kilpelainen,T.O., Koiranen,M.,
            Kolcic,I., Koskinen,S., Kovacs,P., Laitinen,J., Liu,J., Lokki,M.L.,
            Marusic,A., Maschio,A., Meitinger,T., Mulas,A., Pare,G.,
            Parker,A.N., Peden,J.F., Petersmann,A., Pichler,I.,
            Pietilainen,K.H., Pouta,A., Ridderstrale,M., Rotter,J.I.,
            Sambrook,J.G., Sanders,A.R., Schmidt,C.O., Sinisalo,J., Smit,J.H.,
            Stringham,H.M., Bragi Walters,G., Widen,E., Wild,S.H.,
            Willemsen,G., Zagato,L., Zgaga,L., Zitting,P., Alavere,H.,
            Farrall,M., McArdle,W.L., Nelis,M., Peters,M.J., Ripatti,S., van
            Meurs,J.B., Aben,K.K., Ardlie,K.G., Beckmann,J.S., Beilby,J.P.,
            Bergman,R.N., Bergmann,S., Collins,F.S., Cusi,D., den Heijer,M.,
            Eiriksdottir,G., Gejman,P.V., Hall,A.S., Hamsten,A., Huikuri,H.V.,
            Iribarren,C., Kahonen,M., Kaprio,J., Kathiresan,S., Kiemeney,L.,
            Kocher,T., Launer,L.J., Lehtimaki,T., Melander,O., Mosley,T.H. Jr.,
            Musk,A.W., Nieminen,M.S., O'Donnell,C.J., Ohlsson,C., Oostra,B.,
            Palmer,L.J., Raitakari,O., Ridker,P.M., Rioux,J.D., Rissanen,A.,
            Rivolta,C., Schunkert,H., Shuldiner,A.R., Siscovick,D.S.,
            Stumvoll,M., Tonjes,A., Tuomilehto,J., van Ommen,G.J., Viikari,J.,
            Heath,A.C., Martin,N.G., Montgomery,G.W., Province,M.A., Kayser,M.,
            Arnold,A.M., Atwood,L.D., Boerwinkle,E., Chanock,S.J., Deloukas,P.,
            Gieger,C., Gronberg,H., Hall,P., Hattersley,A.T., Hengstenberg,C.,
            Hoffman,W., Lathrop,G.M., Salomaa,V., Schreiber,S., Uda,M.,
            Waterworth,D., Wright,A.F., Assimes,T.L., Barroso,I., Hofman,A.,
            Mohlke,K.L., Boomsma,D.I., Caulfield,M.J., Cupples,L.A.,
            Erdmann,J., Fox,C.S., Gudnason,V., Gyllensten,U., Harris,T.B.,
            Hayes,R.B., Jarvelin,M.R., Mooser,V., Munroe,P.B., Ouwehand,W.H.,
            Penninx,B.W., Pramstaller,P.P., Quertermous,T., Rudan,I.,
            Samani,N.J., Spector,T.D., Volzke,H., Watkins,H., Wilson,J.F.,
            Groop,L.C., Haritunians,T., Hu,F.B., Kaplan,R.C., Metspalu,A.,
            North,K.E., Schlessinger,D., Wareham,N.J., Hunter,D.J.,
            O'Connell,J.R., Strachan,D.P., Wichmann,H.E., Borecki,I.B., van
            Duijn,C.M., Schadt,E.E., Thorsteinsdottir,U., Peltonen,L.,
            Uitterlinden,A.G., Visscher,P.M., Chatterjee,N., Loos,R.J.,
            Boehnke,M., McCarthy,M.I., Ingelsson,E., Lindgren,C.M.,
            Abecasis,G.R., Stefansson,K., Frayling,T.M. and Hirschhorn,J.N.
  TITLE     Hundreds of variants clustered in genomic loci and biological
            pathways affect human height
  JOURNAL   Nature 467 (7317), 832-838 (2010)
   PUBMED   20881960
REFERENCE   3  (bases 1 to 8063)
  AUTHORS   Nilsson,J., Helou,K., Kovacs,A., Bendahl,P.O., Bjursell,G.,
            Ferno,M., Carlsson,P. and Kannius-Janson,M.
  TITLE     Nuclear Janus-activated kinase 2/nuclear factor 1-C2 suppresses
            tumorigenesis and epithelial-to-mesenchymal transition by
            repressing Forkhead box F1
  JOURNAL   Cancer Res. 70 (5), 2020-2029 (2010)
   PUBMED   20145151
  REMARK    GeneRIF: novel role of NF1-C2 in tumor development and
            epithelial-to-mesenchymal transition in breast cancer; NF1-C2 is
            lost during tumor progression and virtully absent from lymph node
            metastases; FoxF1 was was found to be a direct repressed target of
            NF1-C2
REFERENCE   4  (bases 1 to 8063)
  AUTHORS   Udelhoven,M., Leeser,U., Freude,S., Hettich,M.M., Laudes,M.,
            Schnitker,J., Krone,W. and Schubert,M.
  TITLE     Identification of a region in the human IRS2 promoter essential for
            stress induced transcription depending on SP1, NFI binding and ERK
            activation in HepG2 cells
  JOURNAL   J. Mol. Endocrinol. 44 (2), 99-113 (2010)
   PUBMED   19755487
  REMARK    GeneRIF: A specific region (-688 to -611 bp) was discovered in the
            IRS2 promoter essential for basal promoter activity and oxidative
            stress induced transcription depending on ERK activation and SP1
            and NFI binding in human hepatocytes.
REFERENCE   5  (bases 1 to 8063)
  AUTHORS   Plasari,G., Calabrese,A., Dusserre,Y., Gronostajski,R.M.,
            McNair,A., Michalik,L. and Mermod,N.
  TITLE     Nuclear factor I-C links platelet-derived growth factor and
            transforming growth factor beta1 signaling to skin wound healing
            progression
  JOURNAL   Mol. Cell. Biol. 29 (22), 6006-6017 (2009)
   PUBMED   19752192
  REMARK    GeneRIF: These results imply a central role of NFI-C in the
            interplay of the two signaling pathways and in regulation of the
            progression of tissue regeneration.
REFERENCE   6  (bases 1 to 8063)
  AUTHORS   Wenzelides,S., Altmann,H., Wendler,W. and Winnacker,E.L.
  TITLE     CTF5--a new transcriptional activator of the NFI/CTF family
  JOURNAL   Nucleic Acids Res. 24 (12), 2416-2421 (1996)
   PUBMED   8710515
REFERENCE   7  (bases 1 to 8063)
  AUTHORS   Blau,J., Xiao,H., McCracken,S., O'Hare,P., Greenblatt,J. and
            Bentley,D.
  TITLE     Three functional classes of transcriptional activation domain
  JOURNAL   Mol. Cell. Biol. 16 (5), 2044-2055 (1996)
   PUBMED   8628270
REFERENCE   8  (bases 1 to 8063)
  AUTHORS   Qian,F., Kruse,U., Lichter,P. and Sippel,A.E.
  TITLE     Chromosomal localization of the four genes (NFIA, B, C, and X) for
            the human transcription factor nuclear factor I by FISH
  JOURNAL   Genomics 28 (1), 66-73 (1995)
   PUBMED   7590749
REFERENCE   9  (bases 1 to 8063)
  AUTHORS   Nehls,M.C., Grapilon,M.L. and Brenner,D.A.
  TITLE     NF-I/Sp1 switch elements regulate collagen alpha 1(I) gene
            expression
  JOURNAL   DNA Cell Biol. 11 (6), 443-452 (1992)
   PUBMED   1524678
REFERENCE   10 (bases 1 to 8063)
  AUTHORS   Santoro,C., Mermod,N., Andrews,P.C. and Tjian,R.
  TITLE     A family of human CCAAT-box-binding proteins active in
            transcription and DNA replication: cloning and expression of
            multiple cDNAs
  JOURNAL   Nature 334 (6179), 218-224 (1988)
   PUBMED   3398920
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BF763988.1, BC012120.1,
            AK297825.1, AK289885.1, CB053896.1, CK431049.1, AC005551.1 and
            BU727954.1.
            
            Summary: The protein encoded by this gene belongs to the CTF/NF-I
            family. These are dimeric DNA-binding proteins, and function as
            cellular transcription factors and as replication factors for
            adenovirus DNA replication. Alternatively spliced transcript
            variants encoding different isoforms have been described for this
            gene. [provided by RefSeq, Oct 2011].
            
            Transcript Variant: This variant (1) encodes the longest isoform
            (1).
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK297825.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025082 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-8                 BF763988.1         20-27
            9-1339              BC012120.1         1-1331
            1340-1735           AK297825.1         1322-1717
            1736-2137           AK289885.1         1672-2073
            2138-2497           CB053896.1         51-410              c
            2498-3090           CK431049.1         45-637
            3091-7781           AC005551.1         12615-17305
            7782-8063           BU727954.1         1-282               c
FEATURES             Location/Qualifiers
     source          1..8063
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19p13.3"
     gene            1..8063
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /note="nuclear factor I/C (CCAAT-binding transcription
                     factor)"
                     /db_xref="GeneID:4782"
                     /db_xref="HGNC:7786"
                     /db_xref="MIM:600729"
     exon            1..100
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    11..13
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /note="upstream in-frame stop codon"
     variation       46
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200806100"
     variation       52
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:372385803"
     variation       62
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:374182689"
     CDS             71..1597
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /note="isoform 1 is encoded by transcript variant 1;
                     nuclear factor 1 C-type; NF1-C; NF-I/C; TGGCA-binding
                     protein; CCAAT-box-binding transcription factor"
                     /codon_start=1
                     /product="nuclear factor 1 C-type isoform 1"
                     /protein_id="NP_001231931.1"
                     /db_xref="GI:350529396"
                     /db_xref="CCDS:CCDS59330.1"
                     /db_xref="GeneID:4782"
                     /db_xref="HGNC:7786"
                     /db_xref="MIM:600729"
                     /translation="
MYSSPLCLTQDEFHPFIEALLPHVRAFAYTWFNLQARKRKYFKKHEKRMSKDEERAVKDELLGEKPEVKQKWASRLLAKLRKDIRPECREDFVLSITGKKAPGCVLSNPDQKGKMRRIDCLRQADKVWRLDLVMVILFKGIPLESTDGERLVKAAQCGHPVLCVQPHHIGVAVKELDLYLAYFVRERDAEQSGSPRTGMGSDQEDSKPITLDTTDFQESFVTSGVFSVTELIQVSRTPVVTGTGPNFSLGELQGHLAYDLNPASTGLRRTLPSTSSSGSKRHKSGSMEEDVDTSPGGDYYTSPSSPTSSSRNWTEDMEGGISSPVKKTEMDKSPFNSPSPQDSPRLSSFTQHHRPVIAVHSGIARSPHPSSALHFPTTSILPQTASTYFPHTAIRYPPHLNPQDPLKDLVSLACDPASQQPGPLNGSGQLKMPSHCLSAQMLAPPPPGLPRLALPPATKPATTSEGGATSPTSPSYSPPDTSPANRSFVGLGPRDPAGIYQAQSWYLG
"
     misc_feature    71..73
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="N-acetylmethionine; propagated from
                     UniProtKB/Swiss-Prot (P08651.2); acetylation site"
     misc_feature    80..211
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /note="Nuclear factor I protein pre-N-terminus; Region:
                     NfI_DNAbd_pre-N; pfam10524"
                     /db_xref="CDD:151076"
     misc_feature    272..577
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /note="N-terminal Mad Homology 1 (MH1) domain; Region:
                     MH1; cl00055"
                     /db_xref="CDD:206806"
     misc_feature    650..652
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P08651.2); phosphorylation site"
     misc_feature    719..1594
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /note="CTF/NF-I family transcription modulation region;
                     Region: CTF_NFI; pfam00859"
                     /db_xref="CDD:144451"
     misc_feature    950..952
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P08651.2); phosphorylation site"
     misc_feature    1037..1039
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P08651.2); phosphorylation site"
     misc_feature    1067..1069
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P08651.2); phosphorylation site"
     misc_feature    1079..1081
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P08651.2); phosphorylation site"
     misc_feature    1085..1087
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P08651.2); phosphorylation site"
     misc_feature    1097..1099
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P08651.2); phosphorylation site"
     misc_feature    1529..1531
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (P08651.2); phosphorylation site"
     exon            101..632
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       131
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190753458"
     variation       151
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144268546"
     variation       178
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148748813"
     variation       180
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141482719"
     variation       190
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370694661"
     variation       196
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150819987"
     variation       215
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:139273924"
     variation       238
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201762449"
     variation       298
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:144458967"
     variation       362
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146638960"
     variation       373
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367554475"
     variation       376
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369119535"
     variation       384
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61731129"
     variation       442
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199785054"
     variation       496
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146650773"
     variation       511
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372862380"
     variation       538
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375768351"
     variation       548
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201434711"
     variation       560
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200551240"
     variation       562
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11878387"
     variation       567
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138699938"
     variation       613
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201632995"
     variation       619
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372436353"
     variation       620
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201510675"
     variation       623
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369796013"
     variation       630
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201011953"
     exon            633..704
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       636
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:145828739"
     variation       640
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369261498"
     variation       647
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200153960"
     variation       665
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78728474"
     variation       700
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371331059"
     exon            705..779
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       709
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377664780"
     variation       739
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111422145"
     variation       740
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143519997"
     variation       751
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201124721"
     variation       754
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:138225094"
     variation       777
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116865554"
     exon            780..903
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       784
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150930822"
     variation       808
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374471241"
     variation       814
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112569402"
     variation       841
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:373306178"
     variation       864
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:35952068"
     variation       879..880
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:34108601"
     variation       885
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368371894"
     exon            904..1028
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       919
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146070921"
     variation       922
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138945457"
     variation       923
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142790393"
     variation       928
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369569353"
     variation       949..950
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:34937859"
     variation       960
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373904141"
     variation       993
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200221249"
     variation       1012
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377153122"
     variation       1018
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369185182"
     exon            1029..1154
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       1099
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:117114356"
     variation       1104
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200686979"
     variation       1132
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199780384"
     variation       1141
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149374084"
     variation       1144
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375318776"
     exon            1155..1339
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       1183
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138179732"
     variation       1221
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374896582"
     variation       1222
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142781909"
     variation       1225
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201575539"
     variation       1234
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146145775"
     variation       1237
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372361568"
     variation       1246
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200793537"
     variation       1254
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140170107"
     variation       1279
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11671446"
     variation       1282
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142476049"
     variation       1285
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368456734"
     variation       1294
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141932371"
     variation       1312
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1060363"
     variation       1319
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:10412720"
     variation       1339
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372367068"
     exon            1340..1493
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       1384
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376400951"
     variation       1404
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199528650"
     variation       1410
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199905745"
     variation       1436
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201510249"
     variation       1447..1448
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:150025045"
     variation       1460
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76933523"
     variation       1476
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370906966"
     variation       1480
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:373976044"
     exon            1494..1579
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       1501
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76459565"
     variation       1503
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372572344"
     variation       1526
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376511703"
     variation       1569
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368331116"
     exon            1580..8045
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     STS             1587..1712
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH70943"
                     /db_xref="UniSTS:18913"
     variation       1604..1606
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="tct"
                     /db_xref="dbSNP:202152750"
     variation       1646
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374310905"
     variation       1649
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370736060"
     variation       1679
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8047"
     variation       1681
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377580938"
     variation       1738
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62130570"
     variation       1770
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185384063"
     variation       1821
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369618261"
     variation       1829
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143763131"
     variation       1907
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147192339"
     variation       1909..1910
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35103414"
     variation       1969
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:112297811"
     variation       2021
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371877071"
     variation       2306
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35033094"
     variation       2362
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:189392307"
     variation       2372
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376897288"
     variation       2595
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115020939"
     variation       2598
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:4807474"
     variation       2732
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116669109"
     variation       2858
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373175985"
     variation       2878
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74656266"
     variation       2903..2904
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:143359349"
     variation       3003
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:10426917"
     variation       3071
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10426352"
     variation       3118
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140546305"
     variation       3150
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3746298"
     variation       3151
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3746299"
     variation       3169
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:7258954"
     variation       3326
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115534300"
     variation       3353
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6510757"
     variation       3529
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:191016688"
     variation       3542
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12971613"
     variation       3623
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142170418"
     variation       3804
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11673590"
     STS             3818..3949
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH47688"
                     /db_xref="UniSTS:41852"
     variation       3848
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:60093027"
     variation       3948
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:713043"
     variation       3952
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:11666623"
     variation       3965
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61089125"
     variation       3980..3981
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:71782480"
     variation       3991
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaaa"
                     /db_xref="dbSNP:71708589"
     variation       4002..4003
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:59668846"
     variation       4003..4007
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="gatac"
                     /db_xref="dbSNP:146468333"
     variation       4003
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201570343"
     variation       4005
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:369702439"
     variation       4006
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:2392709"
     variation       4007
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373239554"
     variation       4010
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377659423"
     variation       4058
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:56294037"
     variation       4152
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:11541514"
     variation       4226..4230
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaat"
                     /db_xref="dbSNP:142281202"
     variation       4230
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370549069"
     variation       4235
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaat"
                     /db_xref="dbSNP:71731809"
     variation       4235
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:373766499"
     variation       4242
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:377329843"
     variation       4245
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370429651"
     variation       4270
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:10617203"
     variation       4283..4284
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="gg"
                     /db_xref="dbSNP:373260051"
     variation       4510
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150732039"
     variation       4516
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112962670"
     variation       4527
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190974806"
     variation       4594
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112077871"
     variation       4612
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370523643"
     variation       4657
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373678102"
     variation       4708
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371834921"
     variation       4720
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139103336"
     variation       4901
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:116639605"
     variation       5051..5052
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:11388112"
     variation       5051
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201353930"
     variation       5058..5059
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:200434679"
     variation       5063
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375507336"
     variation       5222
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182718334"
     variation       5266
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:376532943"
     variation       5300
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149869150"
     variation       5427
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188692410"
     variation       5438
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191740254"
     variation       5441
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:111606883"
     variation       5486..5487
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:112243853"
     variation       5522
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:73919194"
     variation       5548
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183256663"
     variation       5581
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368229276"
     variation       5641
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202195970"
     variation       5688
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373841623"
     STS             5816..5976
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="A008X33"
                     /db_xref="UniSTS:11659"
     variation       5864
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148735510"
     variation       5893
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188079746"
     variation       5923..5924
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:201187022"
     variation       5929
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8112889"
     variation       5930..5931
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:146782728"
     variation       5930
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8108753"
     variation       5931..5932
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:68098094"
     variation       5933..5934
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:373716537"
     variation       5936
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:148147968"
     variation       5936
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8108755"
     variation       5943..5944
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:59410286"
     variation       5969
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:182356784"
     variation       6041
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:374469121"
     variation       6051
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11357750"
     variation       6083
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:118139977"
     variation       6134
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187795070"
     variation       6137
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:111969590"
     variation       6288
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192533268"
     variation       6450
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:146433383"
     variation       6537
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73919195"
     STS             6561..6697
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="G32369"
                     /db_xref="UniSTS:116958"
     STS             6561..6697
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH67057"
                     /db_xref="UniSTS:84684"
     variation       6586..6587
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatatat"
                     /db_xref="dbSNP:374523932"
     variation       6586..6587
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8110278"
     variation       6586
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:28665162"
     variation       6587..6606
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatat"
                     /db_xref="dbSNP:375414685"
     variation       6587..6588
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatatat"
                     /replace="atatattatatatatatatat"
                     /db_xref="dbSNP:34605422"
     variation       6594
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185019123"
     variation       6609
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190207945"
     variation       6619..6620
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:35325992"
     variation       6652
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8113786"
     variation       6690
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192998513"
     variation       6722
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116148466"
     variation       6762
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:72974787"
     variation       6795
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140704632"
     variation       6820
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:8110928"
     variation       6836
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372237245"
     variation       7018..7019
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:377115512"
     variation       7023
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374793831"
     variation       7026
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369655483"
     variation       7154
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184806177"
     variation       7281
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74741143"
     variation       7333
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4807475"
     variation       7414
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:188683808"
     variation       7443
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376460082"
     variation       7483
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144557238"
     variation       7542..7543
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:199586457"
     variation       7593..7595
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="ctt"
                     /db_xref="dbSNP:370673109"
     variation       7595..7597
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="tct"
                     /db_xref="dbSNP:57761031"
     variation       7605
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:180737599"
     variation       7668
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185090028"
     variation       7768
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369940873"
     variation       7792
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146638802"
     STS             7795..7922
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="WI-12079"
                     /db_xref="UniSTS:15156"
     variation       7799
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35160631"
     STS             7810..7926
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH36034"
                     /db_xref="UniSTS:47850"
     variation       7813
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189164209"
     variation       7832
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:10417031"
     variation       7885
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141326218"
     variation       7908
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11547206"
     variation       7980..7983
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="acaa"
                     /db_xref="dbSNP:199877074"
     variation       7982..7986
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaca"
                     /db_xref="dbSNP:147791651"
     variation       7982
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaca"
                     /db_xref="dbSNP:71715433"
     variation       7985..7989
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:146550572"
     variation       7985
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:10543929"
     variation       7985
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:60861688"
     variation       7989
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:373990617"
     variation       7990..7991
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="ag"
                     /db_xref="dbSNP:71656643"
     variation       7991
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12983451"
     polyA_signal    8020..8025
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
     polyA_site      8045
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
ORIGIN      
tttggaaaaatgactcagtaagttcagcgcgcccgctccggccggccctgcgcctcccgccgcgcccgggatgtattcgtccccgctctgcctcacccaggatgagttccacccgttcatcgaggccctgctgcctcacgtccgcgccttcgcctacacctggttcaacctgcaggcgcggaagcgcaagtacttcaagaagcacgagaagcggatgtcgaaggacgaggagcgtgcggtcaaggacgagctgctgggcgagaagcccgaggtcaagcagaagtgggcgtcgcggctgctggccaagctgcgcaaggacatccggcccgagtgccgcgaggacttcgtgctgagcatcaccggcaagaaggcgccgggctgcgtgctctccaaccccgaccagaagggcaagatgcggcgcatcgactgtctccggcaggcggacaaggtgtggcggctggacctggtcatggtcatcctgttcaagggcatcccgctggagagcaccgacggcgagcgcctggtcaaggctgcgcagtgcggtcacccggtcctgtgcgtgcagccgcaccacattggcgtggccgtcaaggagctggacctctacctggcctacttcgtgcgtgagcgagatgcagagcaaagcggcagtccccggacagggatgggctctgaccaggaggacagcaagcccatcacgctggacacgaccgacttccaggagagctttgtcacctccggcgtgttcagcgtcactgagctcatccaagtgtcccggacacccgtggtgactggaacaggacccaacttctccctgggggagctgcaggggcacctggcatacgacctgaacccagccagcactggcctcagaagaacgctgcccagcacctcctccagtgggagcaagcggcacaaatcgggctcgatggaggaagacgtggacacgagccctggcggcgattactacacttcgcccagctcgcccacgagtagcagccgcaactggacggaggacatggaaggaggcatctcgtccccggtgaagaagacagagatggacaagtcaccattcaacagcccgtccccccaggactctccccgcctctccagcttcacccagcaccaccggcccgtcatcgccgtgcacagcgggatcgcccggagcccacacccgtcctccgctctgcatttccctacgacgtccatcctaccccagacggcctccacctacttcccccacacggccatccgctacccacctcatctcaacccccaggacccgctcaaagatcttgtctcgctggcctgcgacccagccagccagcaacctggaccgttaaatggaagtggtcagctcaaaatgcccagccactgcctttctgctcagatgctggcacctccgcccccggggctgccacggctggcgctcccccctgccaccaaacccgccaccacctccgagggaggagccacgtcgccgacctcgccttcctactctccgcccgacacgtcccctgcaaaccgttcctttgtgggattaggaccaagggatcctgcgggcatttatcaggcacagtcctggtatctgggatagcaaaggtcttcttccctcgccccttctccatcgtcccaggaatcccagggggcagcacagccggcccccggcccacgttttcggtggaaaattagagtgaacaagaacacccctgccgactcccagcccggccaaaaagacaaaacacatagacgcacacactcaggaggaaaagaaaaaacaaaggcagaagaagaagaagaagaaataaaaacccacccaagcaagaagacaaaaggtaaagacgcaacgtttccaactctcgggacgccaaggccgcaggactggagggccaggccccgccacccccacgggagacccgggacagggcgtcttcctaagttattcatctcctctccgcctgctgctcgggaaggacagacgccggccgcccgcccgcgccccggaggccctggctctgtccggagaccaggtgagcacagcctggagcctgtgcccagggccgacaggcgcgacacccagcaaggccacctctccccgggcccccgcgcctctgccggacacggaccggcccctcagcccccaccgaggacgcagccactggggggaaagggagacacagcggaccccggccgggcagcggagaccgcagaggcgggcagggtggggcaggcgagtggtgtcgcgggggtgcgtggcgcttgcgagccctggccaggggaggaagtgaggcccaggcacctgctgcccctcgagggggccctgcctgccgcggggcctccccacaagcccctcccaaagcgccggccgactcgctgtctcgctggggactctttcagccctcgcgcccgcccgtttgggaggagaagtctctatgcaattggccccggcccctccaccccccacccccggcataggaggcccccccacctcgcccggctcacacccccaaagggagggacccacattgcacacactgtaagaaatgcactttccgaggaaggggatgggggagcccggacacccagagctccccgagttgggggtgcccgtctggagcgcccccgtcagcccctggcggtgggaggtgagagcgagtggtttaagtgcctgattaccaccacccgcccccccctttgtccagctgggacacggaatggccgcgggcctcctccccctcccctccagcctctccaccagcccctccagtcaaccctcatcgccgtgcccccccagagctagagagatggggcccctgcgtggcccgaggggcagagctgggcgtcacttcgcaagcgtcctgccctgccggggcgcgggggtgggctctggggaagccggtgcgccccccacgcctccgctgccagtgccttacattctggagcgacccccctccctggtgcctcccagcgaagggggaccgccgtttgcactttcatcgcctaccccgacgcggggcccagctgcgggacgtgcatcacggctgggcccccagaggagagaggaggccgacgccagcggtccccgctcggaacggggagggttttcggggggttcggcgtcgcaccttggggccccccgcagccgtgtagggggcctcccatctgctaagcgtttttccgttgagccgctccaaaaacactaagctggggacgccaggtgcccccccaccccggctccctggccctatccacacctccacccccaccccaggatcgccatctttaggggaggcctgggagggggtgttaggtgttttagggccaccgagctcaaacacaaggacccctccccggcccacccagcccagccccaactgacctccatgcctagggaaaaactccccccaccactgccccctcccccgacccaggccaaagccagggcaggtctccgggtctcacctgctcctagcctcacccccctgcccccgaaaaccagactctcctcccaaactagcctcaggagcttggcgaacccgctcgctcctaaagagaaagacccaggaccctcccccatcacccccaagagaggttcgccatcctctggcctcgagcccttggtccctccgtccgtctgtcctcggggcccgctcccccggtggcccttggggatcaaagcgtgggccgctctccgggagggcgggcgggggagggggtggtcgggttgtgccattggggtgtccggaagcttctcagccagggtgggggtcgtggagtgggggagggaggccagccgggctccagaggggtcagggcgcgacgagaaccaactctttacctaactttgcatggtgcttagtcaaggactcctgcgacctggctcccgaggtcagctggcggcgctgacacacatgcatggcagactatccctggctctatctccctgttcctcgccccctccaccccccacttcctctttaaaaaaaaaaaaaaaaaaaaaaagatacaagaaaaacctttaaaaaaattccatgtttcctaatttgcacgaaattttctaccacaagatgtgccttgccttccgagaataagtattacctttaaacaatatcagcgcacacacatagctgcatgttctgctcgtgtagtttaaaaaaaaaaagacaaaacagtgacatgaaataaaaaataaaaattgaaaagggatgtatttctatttgtaaaaaaaataaaataaaaaataagaaagtgagaatctaaaaaaaaaaaaaaaaaaaaaaaaggaagaaaaaccacgctaaaaatcaagccactgaaaacaattgcccccaggtctacccagcccctggctgtccttggtcctgtctcccctcctgctgtattcaggggtgccccctggtgctcagcctctaccacccccaaccctgctcttgggtacccagaggggtcatttctgaatcccttgcccagaggacagacctccggggcccatcttggccctgggaaagggctctcctctctgattggtccctaggccacgggccggcccccagacaccattcaccgacccactgcaggctgtcctccaaccatggggtggccactccacccgcagccagactccccgctccccacttttcatgcaggctggcatacccctggctcagggtcaaatgctgttccacacccacctcagaggcaccccctctcccctgccccgtgcatccccacccttcttgccaaaggacctcttttcccctatccagagaccaccccaggtggcattctctcccaccttctcctttgtcccccatcccctgtctctgtcttccagctgtgaatatgaagggtatcctgtatgaaacaaaaacaaaacctgatatatgcaatatctgtctgtctgtctgtacccatgggcctggctcagccattggaggcccagccgagggtccggcagggcacagggacagccaggtggcaccgagtcacaggctgtggtccggtggctgagcatgctgttgtcttgtccttgattttattttcttttgttctttttttttttcttttctttttgtttttaactccagcttcctttgctttttacttgaccaaagctaagacaatagccagatggttagtggggcagccaggcagggaggacccagggctgggattctccaaccttaggccattcctgcagccctcaccacctccagcccctccaagcatctcgtgtagggacccacgcagatggtcccattcattcactattgcccccaaccccgggattttgggtggtctccacagccaccatcatacactcatcccgtgttttcttccaaaaagtcacctcagcagcctccccaggcgatacagagggagagcccagaccaccacagctggccacgacattgcccttaagtaatatgcattggccagagagcccgggctggctgtgcacagcattcatgtagctgatttctagctttttttttttttctgccccactcctgagcaaatctgtcttgccaaggaactaggagcaaccggaggcaaagggagtgggtggccccatcactattgggaccatcgcgtccctgcacagcccacacccgggggcccagagtcctgggctggacgccacccttctcaccccgagcttgcctccttggctcacttggcaccttggctgagtacagcaggcaaaagcccataccaggcagcatgttgtggatggtttagttctccccgcctccctgtttcttggaaaagctacagggtccctgtagggcaaaattcccaggcgccttgctgcagacagagtaagacaaaaacaccaggaagcaggattccgtgcccatctctgcagtttgggttcacaaaagggggtgccgtcatccctgggtggaggagggagtgttggttttttgtttttgtttttttaacatgtatgaaactgacatcttctcaaatcttgttccacccccctctggaagcccccatcacccacccctgctatggacaccacacctatgccaggcccccccccccaccccagtctcattctggggtctgcccatgctgtgggaaagaatagggaggcctcccaaatatatgcaaattgtccccattccgtgggggcacctgacaatgacccgggtggagatggggcatggaggagtaggaagacccagccctatttgactggggagaggaggatctggagtccttcatgcccaggtctggaacccaggttctgaccccagggccccaccctgggctggacaatcagatcccaaaggaatgccaaaggggactcggttgggagagccgcttaggggccagacctgggtccccctgcaggtccccaggcagcagacaattccaccttccctgccccaggaccttgagagacagcagcattccaggcacagacagacttggctgcaccccactgtcccttgcaagacaggttctggagccaggagcaactgtccagccctccagaagagacagcaagcagcccccctacccactctggcctccccaatggtactttgacctccagtgtagggctatactatacatatatatatatatatatatatatatatataattttggaatttgtttctcataatacagaatatatagtggctaccttgtatcttggtctggattctctctctgagaccccggattttactttctctttggagggcgctgggacatacatctctcaatccagcttcctccgcatcctcccatcttgccccatttctgccacgtcagacacttcctgagagtctcaccttcaaaatgacaccgctgcccatccattgctcaatggtacagagtgtggggtcagtccaccacccttgacctcccggcagggcaaggtgaggaggcggacccaaagcagtaccagcaggacttgttgccagtgataccaaaacagacttttcccaagcagtgcctcacatgtctgctggtgtggctttgggattctcctgccccacccccccgtccatggcagccccctccccaaggctttgctcacacctgagacaggaaggaggaaggggatccaataggaatatgggccccggaggggaagtcatgcacccccaagccaccaccccccagccttccacgcacatctcctggctggaagagagccctccaaaaaggggacacaggctgccccggcccctcaactgcatccacaccccatcctctcatcttgggtcccagccaggcccccccaaaaccaaagccccctcaagtcctggggtcccagcctgtgcccccagcttcctgcccacccagccctgagcattctcacacagagaaagaacaagcaagggctccagggggacaggatggggcagggcatacagtggggggtgggggggcagctgggaggagggagggacaaaacaaaacattttcctttgggttttttttttctttcttttttctcccctttactctttgggtggtgttgcttttcctttccttttccctttgagatttttttgttgttgtttcctttttgtattttactgatatcaccaggatagtttactctccttctagctttctgcttaccgcacactggataacacacacatacacacccacaaaaatgctcatgaacccaatccggagaaggttccagcaggtcccccaccctcccctcctcctcctacttctcctcttgacagcgaggacaggagggggacaaggggacacctgggcagacccgccggctctccccccaccccaccccgcccctcacatcatactccaatcataaccttgtatattacgcagtcattttggttttcgcggacgcgcctacctaagtaccatttacagaaagtgactctggctgtcattattttgtttatttgttccctatgcaaaaaaaaaatgaaaatgaaaaaagggggattccataaaagattcaataaaagacaaacaaaaaaaaaagaaaaaagaaaaaaatgtataaaaattaaacaagctatgcttcgactcttaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:4782 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA
            GeneID:4782 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IDA
            GeneID:4782 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IDA
            GeneID:4782 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IGI
            GeneID:4782 -> Biological process: GO:0006260 [DNA replication] evidence: IEA
            GeneID:4782 -> Biological process: GO:0006366 [transcription from RNA polymerase II promoter] evidence: TAS
            GeneID:4782 -> Biological process: GO:0042475 [odontogenesis of dentin-containing tooth] evidence: IEA
            GeneID:4782 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IDA
            GeneID:4782 -> Cellular component: GO:0005634 [nucleus] evidence: IEA

by @meso_cacase at DBCLS
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