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2020-10-26 19:48:02, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001245005            7932 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens nuclear factor I/C (CCAAT-binding transcription
            factor) (NFIC), transcript variant 4, mRNA.
ACCESSION   NM_001245005
VERSION     NM_001245005.1  GI:350529404
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 7932)
  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 7932)
  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 7932)
  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 7932)
  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 7932)
  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 7932)
  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 7932)
  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 7932)
  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 7932)
  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 7932)
  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.
            
            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 (4) contains an alternate 5'
            terminal exon, and lacks an exon in the 3' coding region (causing a
            frame-shift) compared to variant 1. This results in translation
            initiation from an alternate start codon, and a shorter isoform (4)
            with distinct N- and C- termini 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 :: AK304816.1 [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
            88-1362             AK289885.1         1-1275
            1363-2006           AK289885.1         1430-2073
            2007-2366           CB053896.1         51-410              c
            2367-2959           CK431049.1         45-637
            2960-7650           AC005551.1         12615-17305
            7651-7932           BU727954.1         1-282               c
FEATURES             Location/Qualifiers
     source          1..7932
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
                     /map="19p13.3"
     gene            1..7932
                     /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..1413
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /note="isoform 4 is encoded by transcript variant 4;
                     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 4"
                     /protein_id="NP_001231934.1"
                     /db_xref="GI:350529405"
                     /db_xref="CCDS:CCDS58640.1"
                     /db_xref="GeneID:4782"
                     /db_xref="HGNC:7786"
                     /db_xref="MIM:600729"
                     /translation="
MDEFHPFIEALLPHVRAFAYTWFNLQARKRKYFKKHEKRMSKDEERAVKDELLGEKPEVKQKWASRLLAKLRKDIRPECREDFVLSITGKKAPGCVLSNPDQKGKMRRIDCLRQADKVWRLDLVMVILFKGIPLESTDGERLVKAAQCGHPVLCVQPHHIGVAVKELDLYLAYFVRERDAEQSGSPRTGMGSDQEDSKPITLDTTDFQESFVTSGVFSVTELIQVSRTPVVTGTGPNFSLGELQGHLAYDLNPASTGLRRTLPSTSSSGSKRHKSGSMEEDVDTSPGGDYYTSPSSPTSSSRNWTEDMEGGISSPVKKTEMDKSPFNSPSPQDSPRLSSFTQHHRPVIAVHSGIARSPHPSSALHFPTTSILPQTASTYFPHTAIRYPPHLNPQDPLKDLVSLACDPASQQPGPPTLRPTRPLQTVPLWD
"
     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    742..>1347
                     /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"
     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..1448
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     variation       1370
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:76459565"
     variation       1372
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372572344"
     variation       1395
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376511703"
     variation       1438
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368331116"
     exon            1449..7914
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /inference="alignment:Splign:1.39.8"
     STS             1456..1581
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH70943"
                     /db_xref="UniSTS:18913"
     variation       1473..1475
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="tct"
                     /db_xref="dbSNP:202152750"
     variation       1515
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:374310905"
     variation       1518
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370736060"
     variation       1548
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8047"
     variation       1550
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377580938"
     variation       1607
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:62130570"
     variation       1639
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185384063"
     variation       1690
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:369618261"
     variation       1698
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:143763131"
     variation       1776
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:147192339"
     variation       1778..1779
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:35103414"
     variation       1838
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:112297811"
     variation       1890
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371877071"
     variation       2175
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:35033094"
     variation       2231
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:189392307"
     variation       2241
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:376897288"
     variation       2464
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:115020939"
     variation       2467
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:4807474"
     variation       2601
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116669109"
     variation       2727
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373175985"
     variation       2747
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:74656266"
     variation       2772..2773
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:143359349"
     variation       2872
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:10426917"
     variation       2940
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:10426352"
     variation       2987
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:140546305"
     variation       3019
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3746298"
     variation       3020
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:3746299"
     variation       3038
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:7258954"
     variation       3195
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:115534300"
     variation       3222
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:6510757"
     variation       3398
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:191016688"
     variation       3411
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12971613"
     variation       3492
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:142170418"
     variation       3673
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:11673590"
     STS             3687..3818
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH47688"
                     /db_xref="UniSTS:41852"
     variation       3717
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:60093027"
     variation       3817
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:713043"
     variation       3821
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:11666623"
     variation       3834
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:61089125"
     variation       3849..3850
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:71782480"
     variation       3860
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaaa"
                     /db_xref="dbSNP:71708589"
     variation       3871..3872
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:59668846"
     variation       3872..3876
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="gatac"
                     /db_xref="dbSNP:146468333"
     variation       3872
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201570343"
     variation       3874
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:369702439"
     variation       3875
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:2392709"
     variation       3876
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373239554"
     variation       3879
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377659423"
     variation       3927
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:56294037"
     variation       4021
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:11541514"
     variation       4095..4099
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaat"
                     /db_xref="dbSNP:142281202"
     variation       4099
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:370549069"
     variation       4104
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaat"
                     /db_xref="dbSNP:71731809"
     variation       4104
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:373766499"
     variation       4111
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:377329843"
     variation       4114
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370429651"
     variation       4139
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="aa"
                     /db_xref="dbSNP:10617203"
     variation       4152..4153
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="gg"
                     /db_xref="dbSNP:373260051"
     variation       4379
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:150732039"
     variation       4385
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:112962670"
     variation       4396
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190974806"
     variation       4463
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112077871"
     variation       4481
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:370523643"
     variation       4526
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:373678102"
     variation       4577
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:371834921"
     variation       4589
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:139103336"
     variation       4770
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:116639605"
     variation       4920..4921
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:11388112"
     variation       4920
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:201353930"
     variation       4927..4928
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:200434679"
     variation       4932
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375507336"
     variation       5091
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:182718334"
     variation       5135
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:376532943"
     variation       5169
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149869150"
     variation       5296
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188692410"
     variation       5307
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:191740254"
     variation       5310
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:111606883"
     variation       5355..5356
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:112243853"
     variation       5391
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:73919194"
     variation       5417
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183256663"
     variation       5450
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368229276"
     variation       5510
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:202195970"
     variation       5557
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:373841623"
     STS             5685..5845
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="A008X33"
                     /db_xref="UniSTS:11659"
     variation       5733
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148735510"
     variation       5762
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:188079746"
     variation       5792..5793
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:201187022"
     variation       5798
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8112889"
     variation       5799..5800
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:146782728"
     variation       5799
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8108753"
     variation       5800..5801
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:68098094"
     variation       5802..5803
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:373716537"
     variation       5805
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:148147968"
     variation       5805
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:8108755"
     variation       5812..5813
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:59410286"
     variation       5838
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:182356784"
     variation       5910
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:374469121"
     variation       5920
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:11357750"
     variation       5952
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:118139977"
     variation       6003
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:187795070"
     variation       6006
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:111969590"
     variation       6157
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192533268"
     variation       6319
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:146433383"
     variation       6406
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:73919195"
     STS             6430..6566
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="G32369"
                     /db_xref="UniSTS:116958"
     STS             6430..6566
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH67057"
                     /db_xref="UniSTS:84684"
     variation       6455..6456
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatatat"
                     /db_xref="dbSNP:374523932"
     variation       6455..6456
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8110278"
     variation       6455
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:28665162"
     variation       6456..6475
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatat"
                     /db_xref="dbSNP:375414685"
     variation       6456..6457
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="atatatatatatatatatatat"
                     /replace="atatattatatatatatatat"
                     /db_xref="dbSNP:34605422"
     variation       6463
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185019123"
     variation       6478
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190207945"
     variation       6488..6489
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="t"
                     /db_xref="dbSNP:35325992"
     variation       6521
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:8113786"
     variation       6559
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192998513"
     variation       6591
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:116148466"
     variation       6631
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:72974787"
     variation       6664
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:140704632"
     variation       6689
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:8110928"
     variation       6705
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:372237245"
     variation       6887..6888
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="c"
                     /db_xref="dbSNP:377115512"
     variation       6892
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:374793831"
     variation       6895
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:369655483"
     variation       7023
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184806177"
     variation       7150
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74741143"
     variation       7202
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4807475"
     variation       7283
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:188683808"
     variation       7312
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376460082"
     variation       7352
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:144557238"
     variation       7411..7412
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="g"
                     /db_xref="dbSNP:199586457"
     variation       7462..7464
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="ctt"
                     /db_xref="dbSNP:370673109"
     variation       7464..7466
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="tct"
                     /db_xref="dbSNP:57761031"
     variation       7474
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:180737599"
     variation       7537
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:185090028"
     variation       7637
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:369940873"
     variation       7661
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146638802"
     STS             7664..7791
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="WI-12079"
                     /db_xref="UniSTS:15156"
     variation       7668
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35160631"
     STS             7679..7795
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /standard_name="RH36034"
                     /db_xref="UniSTS:47850"
     variation       7682
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189164209"
     variation       7701
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:10417031"
     variation       7754
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:141326218"
     variation       7777
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11547206"
     variation       7849..7852
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="acaa"
                     /db_xref="dbSNP:199877074"
     variation       7851..7855
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaca"
                     /db_xref="dbSNP:147791651"
     variation       7851
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="aaaca"
                     /db_xref="dbSNP:71715433"
     variation       7854..7858
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:146550572"
     variation       7854
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:10543929"
     variation       7854
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:60861688"
     variation       7858
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="caaaa"
                     /db_xref="dbSNP:373990617"
     variation       7859..7860
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace=""
                     /replace="ag"
                     /db_xref="dbSNP:71656643"
     variation       7860
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:12983451"
     polyA_signal    7889..7894
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
     polyA_site      7914
                     /gene="NFIC"
                     /gene_synonym="CTF; CTF5; NF-I; NFI"
ORIGIN      
gctcgctccctcccccgcgcgccctccctcgccgcctcctcccgccgcctgcggcccccccctcgccggggaccgagcgcgctcgctccggcgccggcctcgcctcctcgcagcagcgccatggatgagttccacccgttcatcgaggccctgctgcctcacgtccgcgccttcgcctacacctggttcaacctgcaggcgcggaagcgcaagtacttcaagaagcacgagaagcggatgtcgaaggacgaggagcgtgcggtcaaggacgagctgctgggcgagaagcccgaggtcaagcagaagtgggcgtcgcggctgctggccaagctgcgcaaggacatccggcccgagtgccgcgaggacttcgtgctgagcatcaccggcaagaaggcgccgggctgcgtgctctccaaccccgaccagaagggcaagatgcggcgcatcgactgtctccggcaggcggacaaggtgtggcggctggacctggtcatggtcatcctgttcaagggcatcccgctggagagcaccgacggcgagcgcctggtcaaggctgcgcagtgcggtcacccggtcctgtgcgtgcagccgcaccacattggcgtggccgtcaaggagctggacctctacctggcctacttcgtgcgtgagcgagatgcagagcaaagcggcagtccccggacagggatgggctctgaccaggaggacagcaagcccatcacgctggacacgaccgacttccaggagagctttgtcacctccggcgtgttcagcgtcactgagctcatccaagtgtcccggacacccgtggtgactggaacaggacccaacttctccctgggggagctgcaggggcacctggcatacgacctgaacccagccagcactggcctcagaagaacgctgcccagcacctcctccagtgggagcaagcggcacaaatcgggctcgatggaggaagacgtggacacgagccctggcggcgattactacacttcgcccagctcgcccacgagtagcagccgcaactggacggaggacatggaaggaggcatctcgtccccggtgaagaagacagagatggacaagtcaccattcaacagcccgtccccccaggactctccccgcctctccagcttcacccagcaccaccggcccgtcatcgccgtgcacagcgggatcgcccggagcccacacccgtcctccgctctgcatttccctacgacgtccatcctaccccagacggcctccacctacttcccccacacggccatccgctacccacctcatctcaacccccaggacccgctcaaagatcttgtctcgctggcctgcgacccagccagccagcaacctggaccgcctactctccgcccgacacgtcccctgcaaaccgttcctttgtgggattaggaccaagggatcctgcgggcatttatcaggcacagtcctggtatctgggatagcaaaggtcttcttccctcgccccttctccatcgtcccaggaatcccagggggcagcacagccggcccccggcccacgttttcggtggaaaattagagtgaacaagaacacccctgccgactcccagcccggccaaaaagacaaaacacatagacgcacacactcaggaggaaaagaaaaaacaaaggcagaagaagaagaagaagaaataaaaacccacccaagcaagaagacaaaaggtaaagacgcaacgtttccaactctcgggacgccaaggccgcaggactggagggccaggccccgccacccccacgggagacccgggacagggcgtcttcctaagttattcatctcctctccgcctgctgctcgggaaggacagacgccggccgcccgcccgcgccccggaggccctggctctgtccggagaccaggtgagcacagcctggagcctgtgcccagggccgacaggcgcgacacccagcaaggccacctctccccgggcccccgcgcctctgccggacacggaccggcccctcagcccccaccgaggacgcagccactggggggaaagggagacacagcggaccccggccgggcagcggagaccgcagaggcgggcagggtggggcaggcgagtggtgtcgcgggggtgcgtggcgcttgcgagccctggccaggggaggaagtgaggcccaggcacctgctgcccctcgagggggccctgcctgccgcggggcctccccacaagcccctcccaaagcgccggccgactcgctgtctcgctggggactctttcagccctcgcgcccgcccgtttgggaggagaagtctctatgcaattggccccggcccctccaccccccacccccggcataggaggcccccccacctcgcccggctcacacccccaaagggagggacccacattgcacacactgtaagaaatgcactttccgaggaaggggatgggggagcccggacacccagagctccccgagttgggggtgcccgtctggagcgcccccgtcagcccctggcggtgggaggtgagagcgagtggtttaagtgcctgattaccaccacccgcccccccctttgtccagctgggacacggaatggccgcgggcctcctccccctcccctccagcctctccaccagcccctccagtcaaccctcatcgccgtgcccccccagagctagagagatggggcccctgcgtggcccgaggggcagagctgggcgtcacttcgcaagcgtcctgccctgccggggcgcgggggtgggctctggggaagccggtgcgccccccacgcctccgctgccagtgccttacattctggagcgacccccctccctggtgcctcccagcgaagggggaccgccgtttgcactttcatcgcctaccccgacgcggggcccagctgcgggacgtgcatcacggctgggcccccagaggagagaggaggccgacgccagcggtccccgctcggaacggggagggttttcggggggttcggcgtcgcaccttggggccccccgcagccgtgtagggggcctcccatctgctaagcgtttttccgttgagccgctccaaaaacactaagctggggacgccaggtgcccccccaccccggctccctggccctatccacacctccacccccaccccaggatcgccatctttaggggaggcctgggagggggtgttaggtgttttagggccaccgagctcaaacacaaggacccctccccggcccacccagcccagccccaactgacctccatgcctagggaaaaactccccccaccactgccccctcccccgacccaggccaaagccagggcaggtctccgggtctcacctgctcctagcctcacccccctgcccccgaaaaccagactctcctcccaaactagcctcaggagcttggcgaacccgctcgctcctaaagagaaagacccaggaccctcccccatcacccccaagagaggttcgccatcctctggcctcgagcccttggtccctccgtccgtctgtcctcggggcccgctcccccggtggcccttggggatcaaagcgtgggccgctctccgggagggcgggcgggggagggggtggtcgggttgtgccattggggtgtccggaagcttctcagccagggtgggggtcgtggagtgggggagggaggccagccgggctccagaggggtcagggcgcgacgagaaccaactctttacctaactttgcatggtgcttagtcaaggactcctgcgacctggctcccgaggtcagctggcggcgctgacacacatgcatggcagactatccctggctctatctccctgttcctcgccccctccaccccccacttcctctttaaaaaaaaaaaaaaaaaaaaaaagatacaagaaaaacctttaaaaaaattccatgtttcctaatttgcacgaaattttctaccacaagatgtgccttgccttccgagaataagtattacctttaaacaatatcagcgcacacacatagctgcatgttctgctcgtgtagtttaaaaaaaaaaagacaaaacagtgacatgaaataaaaaataaaaattgaaaagggatgtatttctatttgtaaaaaaaataaaataaaaaataagaaagtgagaatctaaaaaaaaaaaaaaaaaaaaaaaaggaagaaaaaccacgctaaaaatcaagccactgaaaacaattgcccccaggtctacccagcccctggctgtccttggtcctgtctcccctcctgctgtattcaggggtgccccctggtgctcagcctctaccacccccaaccctgctcttgggtacccagaggggtcatttctgaatcccttgcccagaggacagacctccggggcccatcttggccctgggaaagggctctcctctctgattggtccctaggccacgggccggcccccagacaccattcaccgacccactgcaggctgtcctccaaccatggggtggccactccacccgcagccagactccccgctccccacttttcatgcaggctggcatacccctggctcagggtcaaatgctgttccacacccacctcagaggcaccccctctcccctgccccgtgcatccccacccttcttgccaaaggacctcttttcccctatccagagaccaccccaggtggcattctctcccaccttctcctttgtcccccatcccctgtctctgtcttccagctgtgaatatgaagggtatcctgtatgaaacaaaaacaaaacctgatatatgcaatatctgtctgtctgtctgtacccatgggcctggctcagccattggaggcccagccgagggtccggcagggcacagggacagccaggtggcaccgagtcacaggctgtggtccggtggctgagcatgctgttgtcttgtccttgattttattttcttttgttctttttttttttcttttctttttgtttttaactccagcttcctttgctttttacttgaccaaagctaagacaatagccagatggttagtggggcagccaggcagggaggacccagggctgggattctccaaccttaggccattcctgcagccctcaccacctccagcccctccaagcatctcgtgtagggacccacgcagatggtcccattcattcactattgcccccaaccccgggattttgggtggtctccacagccaccatcatacactcatcccgtgttttcttccaaaaagtcacctcagcagcctccccaggcgatacagagggagagcccagaccaccacagctggccacgacattgcccttaagtaatatgcattggccagagagcccgggctggctgtgcacagcattcatgtagctgatttctagctttttttttttttctgccccactcctgagcaaatctgtcttgccaaggaactaggagcaaccggaggcaaagggagtgggtggccccatcactattgggaccatcgcgtccctgcacagcccacacccgggggcccagagtcctgggctggacgccacccttctcaccccgagcttgcctccttggctcacttggcaccttggctgagtacagcaggcaaaagcccataccaggcagcatgttgtggatggtttagttctccccgcctccctgtttcttggaaaagctacagggtccctgtagggcaaaattcccaggcgccttgctgcagacagagtaagacaaaaacaccaggaagcaggattccgtgcccatctctgcagtttgggttcacaaaagggggtgccgtcatccctgggtggaggagggagtgttggttttttgtttttgtttttttaacatgtatgaaactgacatcttctcaaatcttgttccacccccctctggaagcccccatcacccacccctgctatggacaccacacctatgccaggcccccccccccaccccagtctcattctggggtctgcccatgctgtgggaaagaatagggaggcctcccaaatatatgcaaattgtccccattccgtgggggcacctgacaatgacccgggtggagatggggcatggaggagtaggaagacccagccctatttgactggggagaggaggatctggagtccttcatgcccaggtctggaacccaggttctgaccccagggccccaccctgggctggacaatcagatcccaaaggaatgccaaaggggactcggttgggagagccgcttaggggccagacctgggtccccctgcaggtccccaggcagcagacaattccaccttccctgccccaggaccttgagagacagcagcattccaggcacagacagacttggctgcaccccactgtcccttgcaagacaggttctggagccaggagcaactgtccagccctccagaagagacagcaagcagcccccctacccactctggcctccccaatggtactttgacctccagtgtagggctatactatacatatatatatatatatatatatatatatataattttggaatttgtttctcataatacagaatatatagtggctaccttgtatcttggtctggattctctctctgagaccccggattttactttctctttggagggcgctgggacatacatctctcaatccagcttcctccgcatcctcccatcttgccccatttctgccacgtcagacacttcctgagagtctcaccttcaaaatgacaccgctgcccatccattgctcaatggtacagagtgtggggtcagtccaccacccttgacctcccggcagggcaaggtgaggaggcggacccaaagcagtaccagcaggacttgttgccagtgataccaaaacagacttttcccaagcagtgcctcacatgtctgctggtgtggctttgggattctcctgccccacccccccgtccatggcagccccctccccaaggctttgctcacacctgagacaggaaggaggaaggggatccaataggaatatgggccccggaggggaagtcatgcacccccaagccaccaccccccagccttccacgcacatctcctggctggaagagagccctccaaaaaggggacacaggctgccccggcccctcaactgcatccacaccccatcctctcatcttgggtcccagccaggcccccccaaaaccaaagccccctcaagtcctggggtcccagcctgtgcccccagcttcctgcccacccagccctgagcattctcacacagagaaagaacaagcaagggctccagggggacaggatggggcagggcatacagtggggggtgggggggcagctgggaggagggagggacaaaacaaaacattttcctttgggttttttttttctttcttttttctcccctttactctttgggtggtgttgcttttcctttccttttccctttgagatttttttgttgttgtttcctttttgtattttactgatatcaccaggatagtttactctccttctagctttctgcttaccgcacactggataacacacacatacacacccacaaaaatgctcatgaacccaatccggagaaggttccagcaggtcccccaccctcccctcctcctcctacttctcctcttgacagcgaggacaggagggggacaaggggacacctgggcagacccgccggctctccccccaccccaccccgcccctcacatcatactccaatcataaccttgtatattacgcagtcattttggttttcgcggacgcgcctacctaagtaccatttacagaaagtgactctggctgtcattattttgtttatttgttccctatgcaaaaaaaaaatgaaaatgaaaaaagggggattccataaaagattcaataaaagacaaacaaaaaaaaaagaaaaaagaaaaaaatgtataaaaattaaacaagctatgcttcgactcttaaaaaaaaaaaaaaaaaa
//

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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