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2025-05-09 16:57:12, 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 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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