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2020-10-26 19:47:11, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001245004            7909 bp    mRNA    linear   PRI 01-MAY-2013
DEFINITION  Homo sapiens nuclear factor I/C (CCAAT-binding transcription
            factor) (NFIC), transcript variant 3, mRNA.
ACCESSION   NM_001245004
VERSION     NM_001245004.1  GI:350529400
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 7909)
  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 7909)
  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 7909)
  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 7909)
  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 7909)
  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 7909)
  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 7909)
  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 7909)
  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 7909)
  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 7909)
  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,
            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 (3) lacks an exon in the 3' coding
            region compared to variant 1. This results in a frame-shift, and a
            shorter isoform (3) with a distinct C-terminus compared to 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 :: AK297867.1 [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
            1340-1983           AK289885.1         1430-2073
            1984-2343           CB053896.1         51-410              c
            2344-2936           CK431049.1         45-637
            2937-7627           AC005551.1         12615-17305
            7628-7909           BU727954.1         1-282               c
FEATURES             Location/Qualifiers
     source          1..7909
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19p13.3"
     gene            1..7909
                     /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..1390
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /note="isoform 3 is encoded by transcript variant 3;
                     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 3"
                     /protein_id="NP_001231933.1"
                     /db_xref="GI:350529401"
                     /db_xref="CCDS:CCDS59331.1"
                     /db_xref="GeneID:4782"
                     /db_xref="HGNC:7786"
                     /db_xref="MIM:600729"
                     /translation="
MYSSPLCLTQDEFHPFIEALLPHVRAFAYTWFNLQARKRKYFKKHEKRMSKDEERAVKDELLGEKPEVKQKWASRLLAKLRKDIRPECREDFVLSITGKKAPGCVLSNPDQKGKMRRIDCLRQADKVWRLDLVMVILFKGIPLESTDGERLVKAAQCGHPVLCVQPHHIGVAVKELDLYLAYFVRERDAEQSGSPRTGMGSDQEDSKPITLDTTDFQESFVTSGVFSVTELIQVSRTPVVTGTGPNFSLGELQGHLAYDLNPASTGLRRTLPSTSSSGSKRHKSGSMEEDVDTSPGGDYYTSPSSPTSSSRNWTEDMEGGISSPVKKTEMDKSPFNSPSPQDSPRLSSFTQHHRPVIAVHSGIARSPHPSSALHFPTTSILPQTASTYFPHTAIRYPPHLNPQDPLKDLVSLACDPASQQPGPPTLRPTRPLQTVPLWD
"
     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..>1324
                     /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"
     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..1425
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       1347
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76459565"
     variation       1349
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372572344"
     variation       1372
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376511703"
     variation       1415
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368331116"
     exon            1426..7891
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     STS             1433..1558
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH70943"
                     /db_xref="UniSTS:18913"
     variation       1450..1452
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="tct"
                     /db_xref="dbSNP:202152750"
     variation       1492
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374310905"
     variation       1495
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370736060"
     variation       1525
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8047"
     variation       1527
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377580938"
     variation       1584
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62130570"
     variation       1616
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185384063"
     variation       1667
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369618261"
     variation       1675
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143763131"
     variation       1753
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147192339"
     variation       1755..1756
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35103414"
     variation       1815
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:112297811"
     variation       1867
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371877071"
     variation       2152
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35033094"
     variation       2208
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:189392307"
     variation       2218
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376897288"
     variation       2441
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115020939"
     variation       2444
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:4807474"
     variation       2578
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116669109"
     variation       2704
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373175985"
     variation       2724
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74656266"
     variation       2749..2750
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:143359349"
     variation       2849
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:10426917"
     variation       2917
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10426352"
     variation       2964
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140546305"
     variation       2996
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3746298"
     variation       2997
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3746299"
     variation       3015
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:7258954"
     variation       3172
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115534300"
     variation       3199
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6510757"
     variation       3375
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:191016688"
     variation       3388
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12971613"
     variation       3469
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142170418"
     variation       3650
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11673590"
     STS             3664..3795
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH47688"
                     /db_xref="UniSTS:41852"
     variation       3694
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:60093027"
     variation       3794
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:713043"
     variation       3798
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:11666623"
     variation       3811
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61089125"
     variation       3826..3827
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:71782480"
     variation       3837
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaaa"
                     /db_xref="dbSNP:71708589"
     variation       3848..3849
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:59668846"
     variation       3849..3853
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="gatac"
                     /db_xref="dbSNP:146468333"
     variation       3849
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201570343"
     variation       3851
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:369702439"
     variation       3852
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:2392709"
     variation       3853
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373239554"
     variation       3856
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377659423"
     variation       3904
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:56294037"
     variation       3998
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:11541514"
     variation       4072..4076
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaat"
                     /db_xref="dbSNP:142281202"
     variation       4076
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370549069"
     variation       4081
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaat"
                     /db_xref="dbSNP:71731809"
     variation       4081
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:373766499"
     variation       4088
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:377329843"
     variation       4091
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370429651"
     variation       4116
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:10617203"
     variation       4129..4130
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="gg"
                     /db_xref="dbSNP:373260051"
     variation       4356
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150732039"
     variation       4362
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112962670"
     variation       4373
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190974806"
     variation       4440
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112077871"
     variation       4458
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370523643"
     variation       4503
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373678102"
     variation       4554
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371834921"
     variation       4566
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139103336"
     variation       4747
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:116639605"
     variation       4897..4898
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:11388112"
     variation       4897
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201353930"
     variation       4904..4905
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:200434679"
     variation       4909
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375507336"
     variation       5068
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182718334"
     variation       5112
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:376532943"
     variation       5146
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149869150"
     variation       5273
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188692410"
     variation       5284
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191740254"
     variation       5287
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:111606883"
     variation       5332..5333
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:112243853"
     variation       5368
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:73919194"
     variation       5394
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183256663"
     variation       5427
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368229276"
     variation       5487
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202195970"
     variation       5534
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373841623"
     STS             5662..5822
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="A008X33"
                     /db_xref="UniSTS:11659"
     variation       5710
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148735510"
     variation       5739
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188079746"
     variation       5769..5770
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:201187022"
     variation       5775
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8112889"
     variation       5776..5777
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:146782728"
     variation       5776
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8108753"
     variation       5777..5778
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:68098094"
     variation       5779..5780
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:373716537"
     variation       5782
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:148147968"
     variation       5782
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8108755"
     variation       5789..5790
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:59410286"
     variation       5815
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:182356784"
     variation       5887
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:374469121"
     variation       5897
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11357750"
     variation       5929
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:118139977"
     variation       5980
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187795070"
     variation       5983
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:111969590"
     variation       6134
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192533268"
     variation       6296
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:146433383"
     variation       6383
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73919195"
     STS             6407..6543
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="G32369"
                     /db_xref="UniSTS:116958"
     STS             6407..6543
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH67057"
                     /db_xref="UniSTS:84684"
     variation       6432..6433
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatatat"
                     /db_xref="dbSNP:374523932"
     variation       6432..6433
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8110278"
     variation       6432
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:28665162"
     variation       6433..6452
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatat"
                     /db_xref="dbSNP:375414685"
     variation       6433..6434
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatatat"
                     /replace="atatattatatatatatatat"
                     /db_xref="dbSNP:34605422"
     variation       6440
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185019123"
     variation       6455
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190207945"
     variation       6465..6466
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:35325992"
     variation       6498
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8113786"
     variation       6536
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192998513"
     variation       6568
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116148466"
     variation       6608
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:72974787"
     variation       6641
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140704632"
     variation       6666
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:8110928"
     variation       6682
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372237245"
     variation       6864..6865
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:377115512"
     variation       6869
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374793831"
     variation       6872
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369655483"
     variation       7000
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184806177"
     variation       7127
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74741143"
     variation       7179
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4807475"
     variation       7260
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:188683808"
     variation       7289
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376460082"
     variation       7329
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144557238"
     variation       7388..7389
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:199586457"
     variation       7439..7441
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="ctt"
                     /db_xref="dbSNP:370673109"
     variation       7441..7443
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="tct"
                     /db_xref="dbSNP:57761031"
     variation       7451
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:180737599"
     variation       7514
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185090028"
     variation       7614
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369940873"
     variation       7638
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146638802"
     STS             7641..7768
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="WI-12079"
                     /db_xref="UniSTS:15156"
     variation       7645
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35160631"
     STS             7656..7772
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH36034"
                     /db_xref="UniSTS:47850"
     variation       7659
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189164209"
     variation       7678
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:10417031"
     variation       7731
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141326218"
     variation       7754
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11547206"
     variation       7826..7829
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="acaa"
                     /db_xref="dbSNP:199877074"
     variation       7828..7832
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaca"
                     /db_xref="dbSNP:147791651"
     variation       7828
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaca"
                     /db_xref="dbSNP:71715433"
     variation       7831..7835
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:146550572"
     variation       7831
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:10543929"
     variation       7831
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:60861688"
     variation       7835
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:373990617"
     variation       7836..7837
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="ag"
                     /db_xref="dbSNP:71656643"
     variation       7837
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12983451"
     polyA_signal    7866..7871
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
     polyA_site      7891
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
ORIGIN      
tttggaaaaatgactcagtaagttcagcgcgcccgctccggccggccctgcgcctcccgccgcgcccgggatgtattcgtccccgctctgcctcacccaggatgagttccacccgttcatcgaggccctgctgcctcacgtccgcgccttcgcctacacctggttcaacctgcaggcgcggaagcgcaagtacttcaagaagcacgagaagcggatgtcgaaggacgaggagcgtgcggtcaaggacgagctgctgggcgagaagcccgaggtcaagcagaagtgggcgtcgcggctgctggccaagctgcgcaaggacatccggcccgagtgccgcgaggacttcgtgctgagcatcaccggcaagaaggcgccgggctgcgtgctctccaaccccgaccagaagggcaagatgcggcgcatcgactgtctccggcaggcggacaaggtgtggcggctggacctggtcatggtcatcctgttcaagggcatcccgctggagagcaccgacggcgagcgcctggtcaaggctgcgcagtgcggtcacccggtcctgtgcgtgcagccgcaccacattggcgtggccgtcaaggagctggacctctacctggcctacttcgtgcgtgagcgagatgcagagcaaagcggcagtccccggacagggatgggctctgaccaggaggacagcaagcccatcacgctggacacgaccgacttccaggagagctttgtcacctccggcgtgttcagcgtcactgagctcatccaagtgtcccggacacccgtggtgactggaacaggacccaacttctccctgggggagctgcaggggcacctggcatacgacctgaacccagccagcactggcctcagaagaacgctgcccagcacctcctccagtgggagcaagcggcacaaatcgggctcgatggaggaagacgtggacacgagccctggcggcgattactacacttcgcccagctcgcccacgagtagcagccgcaactggacggaggacatggaaggaggcatctcgtccccggtgaagaagacagagatggacaagtcaccattcaacagcccgtccccccaggactctccccgcctctccagcttcacccagcaccaccggcccgtcatcgccgtgcacagcgggatcgcccggagcccacacccgtcctccgctctgcatttccctacgacgtccatcctaccccagacggcctccacctacttcccccacacggccatccgctacccacctcatctcaacccccaggacccgctcaaagatcttgtctcgctggcctgcgacccagccagccagcaacctggaccgcctactctccgcccgacacgtcccctgcaaaccgttcctttgtgggattaggaccaagggatcctgcgggcatttatcaggcacagtcctggtatctgggatagcaaaggtcttcttccctcgccccttctccatcgtcccaggaatcccagggggcagcacagccggcccccggcccacgttttcggtggaaaattagagtgaacaagaacacccctgccgactcccagcccggccaaaaagacaaaacacatagacgcacacactcaggaggaaaagaaaaaacaaaggcagaagaagaagaagaagaaataaaaacccacccaagcaagaagacaaaaggtaaagacgcaacgtttccaactctcgggacgccaaggccgcaggactggagggccaggccccgccacccccacgggagacccgggacagggcgtcttcctaagttattcatctcctctccgcctgctgctcgggaaggacagacgccggccgcccgcccgcgccccggaggccctggctctgtccggagaccaggtgagcacagcctggagcctgtgcccagggccgacaggcgcgacacccagcaaggccacctctccccgggcccccgcgcctctgccggacacggaccggcccctcagcccccaccgaggacgcagccactggggggaaagggagacacagcggaccccggccgggcagcggagaccgcagaggcgggcagggtggggcaggcgagtggtgtcgcgggggtgcgtggcgcttgcgagccctggccaggggaggaagtgaggcccaggcacctgctgcccctcgagggggccctgcctgccgcggggcctccccacaagcccctcccaaagcgccggccgactcgctgtctcgctggggactctttcagccctcgcgcccgcccgtttgggaggagaagtctctatgcaattggccccggcccctccaccccccacccccggcataggaggcccccccacctcgcccggctcacacccccaaagggagggacccacattgcacacactgtaagaaatgcactttccgaggaaggggatgggggagcccggacacccagagctccccgagttgggggtgcccgtctggagcgcccccgtcagcccctggcggtgggaggtgagagcgagtggtttaagtgcctgattaccaccacccgcccccccctttgtccagctgggacacggaatggccgcgggcctcctccccctcccctccagcctctccaccagcccctccagtcaaccctcatcgccgtgcccccccagagctagagagatggggcccctgcgtggcccgaggggcagagctgggcgtcacttcgcaagcgtcctgccctgccggggcgcgggggtgggctctggggaagccggtgcgccccccacgcctccgctgccagtgccttacattctggagcgacccccctccctggtgcctcccagcgaagggggaccgccgtttgcactttcatcgcctaccccgacgcggggcccagctgcgggacgtgcatcacggctgggcccccagaggagagaggaggccgacgccagcggtccccgctcggaacggggagggttttcggggggttcggcgtcgcaccttggggccccccgcagccgtgtagggggcctcccatctgctaagcgtttttccgttgagccgctccaaaaacactaagctggggacgccaggtgcccccccaccccggctccctggccctatccacacctccacccccaccccaggatcgccatctttaggggaggcctgggagggggtgttaggtgttttagggccaccgagctcaaacacaaggacccctccccggcccacccagcccagccccaactgacctccatgcctagggaaaaactccccccaccactgccccctcccccgacccaggccaaagccagggcaggtctccgggtctcacctgctcctagcctcacccccctgcccccgaaaaccagactctcctcccaaactagcctcaggagcttggcgaacccgctcgctcctaaagagaaagacccaggaccctcccccatcacccccaagagaggttcgccatcctctggcctcgagcccttggtccctccgtccgtctgtcctcggggcccgctcccccggtggcccttggggatcaaagcgtgggccgctctccgggagggcgggcgggggagggggtggtcgggttgtgccattggggtgtccggaagcttctcagccagggtgggggtcgtggagtgggggagggaggccagccgggctccagaggggtcagggcgcgacgagaaccaactctttacctaactttgcatggtgcttagtcaaggactcctgcgacctggctcccgaggtcagctggcggcgctgacacacatgcatggcagactatccctggctctatctccctgttcctcgccccctccaccccccacttcctctttaaaaaaaaaaaaaaaaaaaaaaagatacaagaaaaacctttaaaaaaattccatgtttcctaatttgcacgaaattttctaccacaagatgtgccttgccttccgagaataagtattacctttaaacaatatcagcgcacacacatagctgcatgttctgctcgtgtagtttaaaaaaaaaaagacaaaacagtgacatgaaataaaaaataaaaattgaaaagggatgtatttctatttgtaaaaaaaataaaataaaaaataagaaagtgagaatctaaaaaaaaaaaaaaaaaaaaaaaaggaagaaaaaccacgctaaaaatcaagccactgaaaacaattgcccccaggtctacccagcccctggctgtccttggtcctgtctcccctcctgctgtattcaggggtgccccctggtgctcagcctctaccacccccaaccctgctcttgggtacccagaggggtcatttctgaatcccttgcccagaggacagacctccggggcccatcttggccctgggaaagggctctcctctctgattggtccctaggccacgggccggcccccagacaccattcaccgacccactgcaggctgtcctccaaccatggggtggccactccacccgcagccagactccccgctccccacttttcatgcaggctggcatacccctggctcagggtcaaatgctgttccacacccacctcagaggcaccccctctcccctgccccgtgcatccccacccttcttgccaaaggacctcttttcccctatccagagaccaccccaggtggcattctctcccaccttctcctttgtcccccatcccctgtctctgtcttccagctgtgaatatgaagggtatcctgtatgaaacaaaaacaaaacctgatatatgcaatatctgtctgtctgtctgtacccatgggcctggctcagccattggaggcccagccgagggtccggcagggcacagggacagccaggtggcaccgagtcacaggctgtggtccggtggctgagcatgctgttgtcttgtccttgattttattttcttttgttctttttttttttcttttctttttgtttttaactccagcttcctttgctttttacttgaccaaagctaagacaatagccagatggttagtggggcagccaggcagggaggacccagggctgggattctccaaccttaggccattcctgcagccctcaccacctccagcccctccaagcatctcgtgtagggacccacgcagatggtcccattcattcactattgcccccaaccccgggattttgggtggtctccacagccaccatcatacactcatcccgtgttttcttccaaaaagtcacctcagcagcctccccaggcgatacagagggagagcccagaccaccacagctggccacgacattgcccttaagtaatatgcattggccagagagcccgggctggctgtgcacagcattcatgtagctgatttctagctttttttttttttctgccccactcctgagcaaatctgtcttgccaaggaactaggagcaaccggaggcaaagggagtgggtggccccatcactattgggaccatcgcgtccctgcacagcccacacccgggggcccagagtcctgggctggacgccacccttctcaccccgagcttgcctccttggctcacttggcaccttggctgagtacagcaggcaaaagcccataccaggcagcatgttgtggatggtttagttctccccgcctccctgtttcttggaaaagctacagggtccctgtagggcaaaattcccaggcgccttgctgcagacagagtaagacaaaaacaccaggaagcaggattccgtgcccatctctgcagtttgggttcacaaaagggggtgccgtcatccctgggtggaggagggagtgttggttttttgtttttgtttttttaacatgtatgaaactgacatcttctcaaatcttgttccacccccctctggaagcccccatcacccacccctgctatggacaccacacctatgccaggcccccccccccaccccagtctcattctggggtctgcccatgctgtgggaaagaatagggaggcctcccaaatatatgcaaattgtccccattccgtgggggcacctgacaatgacccgggtggagatggggcatggaggagtaggaagacccagccctatttgactggggagaggaggatctggagtccttcatgcccaggtctggaacccaggttctgaccccagggccccaccctgggctggacaatcagatcccaaaggaatgccaaaggggactcggttgggagagccgcttaggggccagacctgggtccccctgcaggtccccaggcagcagacaattccaccttccctgccccaggaccttgagagacagcagcattccaggcacagacagacttggctgcaccccactgtcccttgcaagacaggttctggagccaggagcaactgtccagccctccagaagagacagcaagcagcccccctacccactctggcctccccaatggtactttgacctccagtgtagggctatactatacatatatatatatatatatatatatatatataattttggaatttgtttctcataatacagaatatatagtggctaccttgtatcttggtctggattctctctctgagaccccggattttactttctctttggagggcgctgggacatacatctctcaatccagcttcctccgcatcctcccatcttgccccatttctgccacgtcagacacttcctgagagtctcaccttcaaaatgacaccgctgcccatccattgctcaatggtacagagtgtggggtcagtccaccacccttgacctcccggcagggcaaggtgaggaggcggacccaaagcagtaccagcaggacttgttgccagtgataccaaaacagacttttcccaagcagtgcctcacatgtctgctggtgtggctttgggattctcctgccccacccccccgtccatggcagccccctccccaaggctttgctcacacctgagacaggaaggaggaaggggatccaataggaatatgggccccggaggggaagtcatgcacccccaagccaccaccccccagccttccacgcacatctcctggctggaagagagccctccaaaaaggggacacaggctgccccggcccctcaactgcatccacaccccatcctctcatcttgggtcccagccaggcccccccaaaaccaaagccccctcaagtcctggggtcccagcctgtgcccccagcttcctgcccacccagccctgagcattctcacacagagaaagaacaagcaagggctccagggggacaggatggggcagggcatacagtggggggtgggggggcagctgggaggagggagggacaaaacaaaacattttcctttgggttttttttttctttcttttttctcccctttactctttgggtggtgttgcttttcctttccttttccctttgagatttttttgttgttgtttcctttttgtattttactgatatcaccaggatagtttactctccttctagctttctgcttaccgcacactggataacacacacatacacacccacaaaaatgctcatgaacccaatccggagaaggttccagcaggtcccccaccctcccctcctcctcctacttctcctcttgacagcgaggacaggagggggacaaggggacacctgggcagacccgccggctctccccccaccccaccccgcccctcacatcatactccaatcataaccttgtatattacgcagtcattttggttttcgcggacgcgcctacctaagtaccatttacagaaagtgactctggctgtcattattttgtttatttgttccctatgcaaaaaaaaaatgaaaatgaaaaaagggggattccataaaagattcaataaaagacaaacaaaaaaaaaagaaaaaagaaaaaaatgtataaaaattaaacaagctatgcttcgactcttaaaaaaaaaaaaaaaaaa
//

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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