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2020-10-24 07:04:18, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_205843               8086 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens nuclear factor I/C (CCAAT-binding transcription
            factor) (NFIC), transcript variant 2, mRNA.
ACCESSION   NM_205843
VERSION     NM_205843.2  GI:350529394
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 8086)
  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 8086)
  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 8086)
  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 8086)
  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 8086)
  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 8086)
  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 8086)
  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 8086)
  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 8086)
  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 8086)
  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 BP279194.1, AK289885.1,
            CB053896.1, CK431049.1, AC005551.1 and BU727954.1.
            This sequence is a reference standard in the RefSeqGene project.
            On Oct 8, 2011 this sequence version replaced gi:45505150.
            
            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 (2) contains an alternate 5'
            terminal exon compared to variant 1. This results in translation
            initiation from an alternate start codon, and a shorter isoform (2)
            with a distinct N-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 :: AK289885.1, X12492.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025084, ERS025085 [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-87                BP279194.1         1-87
            88-2160             AK289885.1         1-2073
            2161-2520           CB053896.1         51-410              c
            2521-3113           CK431049.1         45-637
            3114-7804           AC005551.1         12615-17305
            7805-8086           BU727954.1         1-282               c
FEATURES             Location/Qualifiers
     source          1..8086
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19p13.3"
     gene            1..8086
                     /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..123
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     CDS             121..1620
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /note="isoform 2 is encoded by transcript variant 2;
                     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 2"
                     /protein_id="NP_995315.1"
                     /db_xref="GI:45505151"
                     /db_xref="CCDS:CCDS45914.1"
                     /db_xref="GeneID:4782"
                     /db_xref="HGNC:7786"
                     /db_xref="MIM:600729"
                     /translation="
MDEFHPFIEALLPHVRAFAYTWFNLQARKRKYFKKHEKRMSKDEERAVKDELLGEKPEVKQKWASRLLAKLRKDIRPECREDFVLSITGKKAPGCVLSNPDQKGKMRRIDCLRQADKVWRLDLVMVILFKGIPLESTDGERLVKAAQCGHPVLCVQPHHIGVAVKELDLYLAYFVRERDAEQSGSPRTGMGSDQEDSKPITLDTTDFQESFVTSGVFSVTELIQVSRTPVVTGTGPNFSLGELQGHLAYDLNPASTGLRRTLPSTSSSGSKRHKSGSMEEDVDTSPGGDYYTSPSSPTSSSRNWTEDMEGGISSPVKKTEMDKSPFNSPSPQDSPRLSSFTQHHRPVIAVHSGIARSPHPSSALHFPTTSILPQTASTYFPHTAIRYPPHLNPQDPLKDLVSLACDPASQQPGPLNGSGQLKMPSHCLSAQMLAPPPPGLPRLALPPATKPATTSEGGATSPTSPSYSPPDTSPANRSFVGLGPRDPAGIYQAQSWYLG
"
     misc_feature    124..234
                     /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    295..600
                     /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    667..669
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    673..675
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    742..1617
                     /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    1060..1062
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    1090..1092
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    1102..1104
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    1108..1110
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     misc_feature    1108..1110
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="phosphorylation site"
     exon            124..655
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       154
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:190753458"
     variation       174
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144268546"
     variation       201
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:148748813"
     variation       203
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:141482719"
     variation       213
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370694661"
     variation       219
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:150819987"
     variation       238
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:139273924"
     variation       261
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201762449"
     variation       321
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:144458967"
     variation       385
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146638960"
     variation       396
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:367554475"
     variation       399
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369119535"
     variation       407
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61731129"
     variation       465
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199785054"
     variation       519
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146650773"
     variation       534
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372862380"
     variation       561
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375768351"
     variation       571
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:201434711"
     variation       583
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200551240"
     variation       585
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11878387"
     variation       590
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138699938"
     variation       636
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201632995"
     variation       642
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372436353"
     variation       643
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201510675"
     variation       646
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369796013"
     variation       653
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201011953"
     exon            656..727
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       659
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:145828739"
     variation       663
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369261498"
     variation       670
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200153960"
     variation       688
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:78728474"
     variation       723
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371331059"
     exon            728..802
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       732
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377664780"
     variation       762
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:111422145"
     variation       763
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143519997"
     variation       774
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201124721"
     variation       777
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:138225094"
     variation       800
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:116865554"
     exon            803..926
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       807
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:150930822"
     variation       831
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374471241"
     variation       837
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112569402"
     variation       864
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:373306178"
     variation       887
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:35952068"
     variation       902..903
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:34108601"
     variation       908
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:368371894"
     exon            927..1051
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       942
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:146070921"
     variation       945
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:138945457"
     variation       946
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142790393"
     variation       951
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369569353"
     variation       972..973
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:34937859"
     variation       983
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373904141"
     variation       1016
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200221249"
     variation       1035
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:377153122"
     variation       1041
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:369185182"
     exon            1052..1177
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       1122
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:117114356"
     variation       1127
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200686979"
     variation       1155
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:199780384"
     variation       1164
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149374084"
     variation       1167
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375318776"
     exon            1178..1362
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       1206
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138179732"
     variation       1244
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:374896582"
     variation       1245
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142781909"
     variation       1248
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:201575539"
     variation       1257
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146145775"
     variation       1260
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372361568"
     variation       1269
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200793537"
     variation       1277
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140170107"
     variation       1302
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11671446"
     variation       1305
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:142476049"
     variation       1308
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368456734"
     variation       1317
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141932371"
     variation       1335
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1060363"
     variation       1342
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:10412720"
     variation       1362
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:372367068"
     exon            1363..1516
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       1407
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376400951"
     variation       1427
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199528650"
     variation       1433
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:199905745"
     variation       1459
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201510249"
     variation       1470..1471
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:150025045"
     variation       1483
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:76933523"
     variation       1499
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:370906966"
     variation       1503
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:373976044"
     exon            1517..1602
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       1524
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76459565"
     variation       1526
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372572344"
     variation       1549
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376511703"
     variation       1592
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368331116"
     exon            1603..8068
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     STS             1610..1735
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH70943"
                     /db_xref="UniSTS:18913"
     variation       1627..1629
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="tct"
                     /db_xref="dbSNP:202152750"
     variation       1669
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374310905"
     variation       1672
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370736060"
     variation       1702
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8047"
     variation       1704
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377580938"
     variation       1761
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62130570"
     variation       1793
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185384063"
     variation       1844
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369618261"
     variation       1852
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143763131"
     variation       1930
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147192339"
     variation       1932..1933
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35103414"
     variation       1992
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:112297811"
     variation       2044
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371877071"
     variation       2329
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35033094"
     variation       2385
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:189392307"
     variation       2395
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376897288"
     variation       2618
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115020939"
     variation       2621
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:4807474"
     variation       2755
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116669109"
     variation       2881
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373175985"
     variation       2901
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74656266"
     variation       2926..2927
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:143359349"
     variation       3026
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:10426917"
     variation       3094
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10426352"
     variation       3141
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140546305"
     variation       3173
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3746298"
     variation       3174
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3746299"
     variation       3192
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:7258954"
     variation       3349
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115534300"
     variation       3376
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6510757"
     variation       3552
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:191016688"
     variation       3565
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12971613"
     variation       3646
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142170418"
     variation       3827
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11673590"
     STS             3841..3972
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH47688"
                     /db_xref="UniSTS:41852"
     variation       3871
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:60093027"
     variation       3971
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:713043"
     variation       3975
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:11666623"
     variation       3988
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61089125"
     variation       4003..4004
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:71782480"
     variation       4014
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaaa"
                     /db_xref="dbSNP:71708589"
     variation       4025..4026
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:59668846"
     variation       4026..4030
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="gatac"
                     /db_xref="dbSNP:146468333"
     variation       4026
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201570343"
     variation       4028
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:369702439"
     variation       4029
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:2392709"
     variation       4030
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373239554"
     variation       4033
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377659423"
     variation       4081
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:56294037"
     variation       4175
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:11541514"
     variation       4249..4253
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaat"
                     /db_xref="dbSNP:142281202"
     variation       4253
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370549069"
     variation       4258
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaat"
                     /db_xref="dbSNP:71731809"
     variation       4258
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:373766499"
     variation       4265
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:377329843"
     variation       4268
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370429651"
     variation       4293
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:10617203"
     variation       4306..4307
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="gg"
                     /db_xref="dbSNP:373260051"
     variation       4533
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150732039"
     variation       4539
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112962670"
     variation       4550
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190974806"
     variation       4617
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112077871"
     variation       4635
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370523643"
     variation       4680
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373678102"
     variation       4731
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371834921"
     variation       4743
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139103336"
     variation       4924
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:116639605"
     variation       5074..5075
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:11388112"
     variation       5074
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201353930"
     variation       5081..5082
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:200434679"
     variation       5086
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375507336"
     variation       5245
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182718334"
     variation       5289
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:376532943"
     variation       5323
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149869150"
     variation       5450
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188692410"
     variation       5461
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191740254"
     variation       5464
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:111606883"
     variation       5509..5510
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:112243853"
     variation       5545
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:73919194"
     variation       5571
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183256663"
     variation       5604
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368229276"
     variation       5664
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202195970"
     variation       5711
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373841623"
     STS             5839..5999
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="A008X33"
                     /db_xref="UniSTS:11659"
     variation       5887
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148735510"
     variation       5916
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188079746"
     variation       5946..5947
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:201187022"
     variation       5952
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8112889"
     variation       5953..5954
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:146782728"
     variation       5953
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8108753"
     variation       5954..5955
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:68098094"
     variation       5956..5957
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:373716537"
     variation       5959
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:148147968"
     variation       5959
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8108755"
     variation       5966..5967
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:59410286"
     variation       5992
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:182356784"
     variation       6064
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:374469121"
     variation       6074
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11357750"
     variation       6106
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:118139977"
     variation       6157
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187795070"
     variation       6160
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:111969590"
     variation       6311
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192533268"
     variation       6473
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:146433383"
     variation       6560
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73919195"
     STS             6584..6720
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="G32369"
                     /db_xref="UniSTS:116958"
     STS             6584..6720
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH67057"
                     /db_xref="UniSTS:84684"
     variation       6609..6610
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatatat"
                     /db_xref="dbSNP:374523932"
     variation       6609..6610
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8110278"
     variation       6609
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:28665162"
     variation       6610..6629
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatat"
                     /db_xref="dbSNP:375414685"
     variation       6610..6611
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatatat"
                     /replace="atatattatatatatatatat"
                     /db_xref="dbSNP:34605422"
     variation       6617
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185019123"
     variation       6632
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190207945"
     variation       6642..6643
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:35325992"
     variation       6675
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8113786"
     variation       6713
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192998513"
     variation       6745
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116148466"
     variation       6785
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:72974787"
     variation       6818
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140704632"
     variation       6843
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:8110928"
     variation       6859
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372237245"
     variation       7041..7042
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:377115512"
     variation       7046
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374793831"
     variation       7049
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369655483"
     variation       7177
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184806177"
     variation       7304
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74741143"
     variation       7356
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4807475"
     variation       7437
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:188683808"
     variation       7466
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376460082"
     variation       7506
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144557238"
     variation       7565..7566
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:199586457"
     variation       7616..7618
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="ctt"
                     /db_xref="dbSNP:370673109"
     variation       7618..7620
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="tct"
                     /db_xref="dbSNP:57761031"
     variation       7628
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:180737599"
     variation       7691
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185090028"
     variation       7791
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369940873"
     variation       7815
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146638802"
     STS             7818..7945
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="WI-12079"
                     /db_xref="UniSTS:15156"
     variation       7822
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35160631"
     STS             7833..7949
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH36034"
                     /db_xref="UniSTS:47850"
     variation       7836
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189164209"
     variation       7855
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:10417031"
     variation       7908
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141326218"
     variation       7931
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11547206"
     variation       8003..8006
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="acaa"
                     /db_xref="dbSNP:199877074"
     variation       8005..8009
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaca"
                     /db_xref="dbSNP:147791651"
     variation       8005
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaca"
                     /db_xref="dbSNP:71715433"
     variation       8008..8012
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:146550572"
     variation       8008
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:10543929"
     variation       8008
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:60861688"
     variation       8012
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:373990617"
     variation       8013..8014
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="ag"
                     /db_xref="dbSNP:71656643"
     variation       8014
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12983451"
     polyA_signal    8043..8048
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
     polyA_site      8068
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
ORIGIN      
gctcgctccctcccccgcgcgccctccctcgccgcctcctcccgccgcctgcggcccccccctcgccggggaccgagcgcgctcgctccggcgccggcctcgcctcctcgcagcagcgccatggatgagttccacccgttcatcgaggccctgctgcctcacgtccgcgccttcgcctacacctggttcaacctgcaggcgcggaagcgcaagtacttcaagaagcacgagaagcggatgtcgaaggacgaggagcgtgcggtcaaggacgagctgctgggcgagaagcccgaggtcaagcagaagtgggcgtcgcggctgctggccaagctgcgcaaggacatccggcccgagtgccgcgaggacttcgtgctgagcatcaccggcaagaaggcgccgggctgcgtgctctccaaccccgaccagaagggcaagatgcggcgcatcgactgtctccggcaggcggacaaggtgtggcggctggacctggtcatggtcatcctgttcaagggcatcccgctggagagcaccgacggcgagcgcctggtcaaggctgcgcagtgcggtcacccggtcctgtgcgtgcagccgcaccacattggcgtggccgtcaaggagctggacctctacctggcctacttcgtgcgtgagcgagatgcagagcaaagcggcagtccccggacagggatgggctctgaccaggaggacagcaagcccatcacgctggacacgaccgacttccaggagagctttgtcacctccggcgtgttcagcgtcactgagctcatccaagtgtcccggacacccgtggtgactggaacaggacccaacttctccctgggggagctgcaggggcacctggcatacgacctgaacccagccagcactggcctcagaagaacgctgcccagcacctcctccagtgggagcaagcggcacaaatcgggctcgatggaggaagacgtggacacgagccctggcggcgattactacacttcgcccagctcgcccacgagtagcagccgcaactggacggaggacatggaaggaggcatctcgtccccggtgaagaagacagagatggacaagtcaccattcaacagcccgtccccccaggactctccccgcctctccagcttcacccagcaccaccggcccgtcatcgccgtgcacagcgggatcgcccggagcccacacccgtcctccgctctgcatttccctacgacgtccatcctaccccagacggcctccacctacttcccccacacggccatccgctacccacctcatctcaacccccaggacccgctcaaagatcttgtctcgctggcctgcgacccagccagccagcaacctggaccgttaaatggaagtggtcagctcaaaatgcccagccactgcctttctgctcagatgctggcacctccgcccccggggctgccacggctggcgctcccccctgccaccaaacccgccaccacctccgagggaggagccacgtcgccgacctcgccttcctactctccgcccgacacgtcccctgcaaaccgttcctttgtgggattaggaccaagggatcctgcgggcatttatcaggcacagtcctggtatctgggatagcaaaggtcttcttccctcgccccttctccatcgtcccaggaatcccagggggcagcacagccggcccccggcccacgttttcggtggaaaattagagtgaacaagaacacccctgccgactcccagcccggccaaaaagacaaaacacatagacgcacacactcaggaggaaaagaaaaaacaaaggcagaagaagaagaagaagaaataaaaacccacccaagcaagaagacaaaaggtaaagacgcaacgtttccaactctcgggacgccaaggccgcaggactggagggccaggccccgccacccccacgggagacccgggacagggcgtcttcctaagttattcatctcctctccgcctgctgctcgggaaggacagacgccggccgcccgcccgcgccccggaggccctggctctgtccggagaccaggtgagcacagcctggagcctgtgcccagggccgacaggcgcgacacccagcaaggccacctctccccgggcccccgcgcctctgccggacacggaccggcccctcagcccccaccgaggacgcagccactggggggaaagggagacacagcggaccccggccgggcagcggagaccgcagaggcgggcagggtggggcaggcgagtggtgtcgcgggggtgcgtggcgcttgcgagccctggccaggggaggaagtgaggcccaggcacctgctgcccctcgagggggccctgcctgccgcggggcctccccacaagcccctcccaaagcgccggccgactcgctgtctcgctggggactctttcagccctcgcgcccgcccgtttgggaggagaagtctctatgcaattggccccggcccctccaccccccacccccggcataggaggcccccccacctcgcccggctcacacccccaaagggagggacccacattgcacacactgtaagaaatgcactttccgaggaaggggatgggggagcccggacacccagagctccccgagttgggggtgcccgtctggagcgcccccgtcagcccctggcggtgggaggtgagagcgagtggtttaagtgcctgattaccaccacccgcccccccctttgtccagctgggacacggaatggccgcgggcctcctccccctcccctccagcctctccaccagcccctccagtcaaccctcatcgccgtgcccccccagagctagagagatggggcccctgcgtggcccgaggggcagagctgggcgtcacttcgcaagcgtcctgccctgccggggcgcgggggtgggctctggggaagccggtgcgccccccacgcctccgctgccagtgccttacattctggagcgacccccctccctggtgcctcccagcgaagggggaccgccgtttgcactttcatcgcctaccccgacgcggggcccagctgcgggacgtgcatcacggctgggcccccagaggagagaggaggccgacgccagcggtccccgctcggaacggggagggttttcggggggttcggcgtcgcaccttggggccccccgcagccgtgtagggggcctcccatctgctaagcgtttttccgttgagccgctccaaaaacactaagctggggacgccaggtgcccccccaccccggctccctggccctatccacacctccacccccaccccaggatcgccatctttaggggaggcctgggagggggtgttaggtgttttagggccaccgagctcaaacacaaggacccctccccggcccacccagcccagccccaactgacctccatgcctagggaaaaactccccccaccactgccccctcccccgacccaggccaaagccagggcaggtctccgggtctcacctgctcctagcctcacccccctgcccccgaaaaccagactctcctcccaaactagcctcaggagcttggcgaacccgctcgctcctaaagagaaagacccaggaccctcccccatcacccccaagagaggttcgccatcctctggcctcgagcccttggtccctccgtccgtctgtcctcggggcccgctcccccggtggcccttggggatcaaagcgtgggccgctctccgggagggcgggcgggggagggggtggtcgggttgtgccattggggtgtccggaagcttctcagccagggtgggggtcgtggagtgggggagggaggccagccgggctccagaggggtcagggcgcgacgagaaccaactctttacctaactttgcatggtgcttagtcaaggactcctgcgacctggctcccgaggtcagctggcggcgctgacacacatgcatggcagactatccctggctctatctccctgttcctcgccccctccaccccccacttcctctttaaaaaaaaaaaaaaaaaaaaaaagatacaagaaaaacctttaaaaaaattccatgtttcctaatttgcacgaaattttctaccacaagatgtgccttgccttccgagaataagtattacctttaaacaatatcagcgcacacacatagctgcatgttctgctcgtgtagtttaaaaaaaaaaagacaaaacagtgacatgaaataaaaaataaaaattgaaaagggatgtatttctatttgtaaaaaaaataaaataaaaaataagaaagtgagaatctaaaaaaaaaaaaaaaaaaaaaaaaggaagaaaaaccacgctaaaaatcaagccactgaaaacaattgcccccaggtctacccagcccctggctgtccttggtcctgtctcccctcctgctgtattcaggggtgccccctggtgctcagcctctaccacccccaaccctgctcttgggtacccagaggggtcatttctgaatcccttgcccagaggacagacctccggggcccatcttggccctgggaaagggctctcctctctgattggtccctaggccacgggccggcccccagacaccattcaccgacccactgcaggctgtcctccaaccatggggtggccactccacccgcagccagactccccgctccccacttttcatgcaggctggcatacccctggctcagggtcaaatgctgttccacacccacctcagaggcaccccctctcccctgccccgtgcatccccacccttcttgccaaaggacctcttttcccctatccagagaccaccccaggtggcattctctcccaccttctcctttgtcccccatcccctgtctctgtcttccagctgtgaatatgaagggtatcctgtatgaaacaaaaacaaaacctgatatatgcaatatctgtctgtctgtctgtacccatgggcctggctcagccattggaggcccagccgagggtccggcagggcacagggacagccaggtggcaccgagtcacaggctgtggtccggtggctgagcatgctgttgtcttgtccttgattttattttcttttgttctttttttttttcttttctttttgtttttaactccagcttcctttgctttttacttgaccaaagctaagacaatagccagatggttagtggggcagccaggcagggaggacccagggctgggattctccaaccttaggccattcctgcagccctcaccacctccagcccctccaagcatctcgtgtagggacccacgcagatggtcccattcattcactattgcccccaaccccgggattttgggtggtctccacagccaccatcatacactcatcccgtgttttcttccaaaaagtcacctcagcagcctccccaggcgatacagagggagagcccagaccaccacagctggccacgacattgcccttaagtaatatgcattggccagagagcccgggctggctgtgcacagcattcatgtagctgatttctagctttttttttttttctgccccactcctgagcaaatctgtcttgccaaggaactaggagcaaccggaggcaaagggagtgggtggccccatcactattgggaccatcgcgtccctgcacagcccacacccgggggcccagagtcctgggctggacgccacccttctcaccccgagcttgcctccttggctcacttggcaccttggctgagtacagcaggcaaaagcccataccaggcagcatgttgtggatggtttagttctccccgcctccctgtttcttggaaaagctacagggtccctgtagggcaaaattcccaggcgccttgctgcagacagagtaagacaaaaacaccaggaagcaggattccgtgcccatctctgcagtttgggttcacaaaagggggtgccgtcatccctgggtggaggagggagtgttggttttttgtttttgtttttttaacatgtatgaaactgacatcttctcaaatcttgttccacccccctctggaagcccccatcacccacccctgctatggacaccacacctatgccaggcccccccccccaccccagtctcattctggggtctgcccatgctgtgggaaagaatagggaggcctcccaaatatatgcaaattgtccccattccgtgggggcacctgacaatgacccgggtggagatggggcatggaggagtaggaagacccagccctatttgactggggagaggaggatctggagtccttcatgcccaggtctggaacccaggttctgaccccagggccccaccctgggctggacaatcagatcccaaaggaatgccaaaggggactcggttgggagagccgcttaggggccagacctgggtccccctgcaggtccccaggcagcagacaattccaccttccctgccccaggaccttgagagacagcagcattccaggcacagacagacttggctgcaccccactgtcccttgcaagacaggttctggagccaggagcaactgtccagccctccagaagagacagcaagcagcccccctacccactctggcctccccaatggtactttgacctccagtgtagggctatactatacatatatatatatatatatatatatatatataattttggaatttgtttctcataatacagaatatatagtggctaccttgtatcttggtctggattctctctctgagaccccggattttactttctctttggagggcgctgggacatacatctctcaatccagcttcctccgcatcctcccatcttgccccatttctgccacgtcagacacttcctgagagtctcaccttcaaaatgacaccgctgcccatccattgctcaatggtacagagtgtggggtcagtccaccacccttgacctcccggcagggcaaggtgaggaggcggacccaaagcagtaccagcaggacttgttgccagtgataccaaaacagacttttcccaagcagtgcctcacatgtctgctggtgtggctttgggattctcctgccccacccccccgtccatggcagccccctccccaaggctttgctcacacctgagacaggaaggaggaaggggatccaataggaatatgggccccggaggggaagtcatgcacccccaagccaccaccccccagccttccacgcacatctcctggctggaagagagccctccaaaaaggggacacaggctgccccggcccctcaactgcatccacaccccatcctctcatcttgggtcccagccaggcccccccaaaaccaaagccccctcaagtcctggggtcccagcctgtgcccccagcttcctgcccacccagccctgagcattctcacacagagaaagaacaagcaagggctccagggggacaggatggggcagggcatacagtggggggtgggggggcagctgggaggagggagggacaaaacaaaacattttcctttgggttttttttttctttcttttttctcccctttactctttgggtggtgttgcttttcctttccttttccctttgagatttttttgttgttgtttcctttttgtattttactgatatcaccaggatagtttactctccttctagctttctgcttaccgcacactggataacacacacatacacacccacaaaaatgctcatgaacccaatccggagaaggttccagcaggtcccccaccctcccctcctcctcctacttctcctcttgacagcgaggacaggagggggacaaggggacacctgggcagacccgccggctctccccccaccccaccccgcccctcacatcatactccaatcataaccttgtatattacgcagtcattttggttttcgcggacgcgcctacctaagtaccatttacagaaagtgactctggctgtcattattttgtttatttgttccctatgcaaaaaaaaaatgaaaatgaaaaaagggggattccataaaagattcaataaaagacaaacaaaaaaaaaagaaaaaagaaaaaaatgtataaaaattaaacaagctatgcttcgactcttaaaaaaaaaaaaaaaaaa
//

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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