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2025-05-09 16:47:07, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001245004 7909 bp mRNA linear PRI 01-MAY-2013
DEFINITION Homo sapiens nuclear factor I/C (CCAAT-binding transcription
factor) (NFIC), transcript variant 3, mRNA.
ACCESSION NM_001245004
VERSION NM_001245004.1 GI:350529400
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 7909)
AUTHORS Duval,C., Gaudreault,M., Vigneault,F., Touzel-Deschenes,L.,
Rochette,P.J., Masson-Gadais,B., Germain,L. and Guerin,S.L.
TITLE Rescue of the transcription factors Sp1 and NFI in human skin
keratinocytes through a feeder-layer-dependent suppression of the
proteasome activity
JOURNAL J. Mol. Biol. 418 (5), 281-299 (2012)
PUBMED 22420942
REMARK GeneRIF: the influence of i3T3 on the expression and DNA binding of
NFI, another TF important for cell proliferation and cell cycle
progression
REFERENCE 2 (bases 1 to 7909)
AUTHORS Lango Allen,H., Estrada,K., Lettre,G., Berndt,S.I., Weedon,M.N.,
Rivadeneira,F., Willer,C.J., Jackson,A.U., Vedantam,S.,
Raychaudhuri,S., Ferreira,T., Wood,A.R., Weyant,R.J., Segre,A.V.,
Speliotes,E.K., Wheeler,E., Soranzo,N., Park,J.H., Yang,J.,
Gudbjartsson,D., Heard-Costa,N.L., Randall,J.C., Qi,L., Vernon
Smith,A., Magi,R., Pastinen,T., Liang,L., Heid,I.M., Luan,J.,
Thorleifsson,G., Winkler,T.W., Goddard,M.E., Sin Lo,K., Palmer,C.,
Workalemahu,T., Aulchenko,Y.S., Johansson,A., Zillikens,M.C.,
Feitosa,M.F., Esko,T., Johnson,T., Ketkar,S., Kraft,P., Mangino,M.,
Prokopenko,I., Absher,D., Albrecht,E., Ernst,F., Glazer,N.L.,
Hayward,C., Hottenga,J.J., Jacobs,K.B., Knowles,J.W., Kutalik,Z.,
Monda,K.L., Polasek,O., Preuss,M., Rayner,N.W., Robertson,N.R.,
Steinthorsdottir,V., Tyrer,J.P., Voight,B.F., Wiklund,F., Xu,J.,
Zhao,J.H., Nyholt,D.R., Pellikka,N., Perola,M., Perry,J.R.,
Surakka,I., Tammesoo,M.L., Altmaier,E.L., Amin,N., Aspelund,T.,
Bhangale,T., Boucher,G., Chasman,D.I., Chen,C., Coin,L.,
Cooper,M.N., Dixon,A.L., Gibson,Q., Grundberg,E., Hao,K., Juhani
Junttila,M., Kaplan,L.M., Kettunen,J., Konig,I.R., Kwan,T.,
Lawrence,R.W., Levinson,D.F., Lorentzon,M., McKnight,B.,
Morris,A.P., Muller,M., Suh Ngwa,J., Purcell,S., Rafelt,S.,
Salem,R.M., Salvi,E., Sanna,S., Shi,J., Sovio,U., Thompson,J.R.,
Turchin,M.C., Vandenput,L., Verlaan,D.J., Vitart,V., White,C.C.,
Ziegler,A., Almgren,P., Balmforth,A.J., Campbell,H., Citterio,L.,
De Grandi,A., Dominiczak,A., Duan,J., Elliott,P., Elosua,R.,
Eriksson,J.G., Freimer,N.B., Geus,E.J., Glorioso,N., Haiqing,S.,
Hartikainen,A.L., Havulinna,A.S., Hicks,A.A., Hui,J., Igl,W.,
Illig,T., Jula,A., Kajantie,E., Kilpelainen,T.O., Koiranen,M.,
Kolcic,I., Koskinen,S., Kovacs,P., Laitinen,J., Liu,J., Lokki,M.L.,
Marusic,A., Maschio,A., Meitinger,T., Mulas,A., Pare,G.,
Parker,A.N., Peden,J.F., Petersmann,A., Pichler,I.,
Pietilainen,K.H., Pouta,A., Ridderstrale,M., Rotter,J.I.,
Sambrook,J.G., Sanders,A.R., Schmidt,C.O., Sinisalo,J., Smit,J.H.,
Stringham,H.M., Bragi Walters,G., Widen,E., Wild,S.H.,
Willemsen,G., Zagato,L., Zgaga,L., Zitting,P., Alavere,H.,
Farrall,M., McArdle,W.L., Nelis,M., Peters,M.J., Ripatti,S., van
Meurs,J.B., Aben,K.K., Ardlie,K.G., Beckmann,J.S., Beilby,J.P.,
Bergman,R.N., Bergmann,S., Collins,F.S., Cusi,D., den Heijer,M.,
Eiriksdottir,G., Gejman,P.V., Hall,A.S., Hamsten,A., Huikuri,H.V.,
Iribarren,C., Kahonen,M., Kaprio,J., Kathiresan,S., Kiemeney,L.,
Kocher,T., Launer,L.J., Lehtimaki,T., Melander,O., Mosley,T.H. Jr.,
Musk,A.W., Nieminen,M.S., O'Donnell,C.J., Ohlsson,C., Oostra,B.,
Palmer,L.J., Raitakari,O., Ridker,P.M., Rioux,J.D., Rissanen,A.,
Rivolta,C., Schunkert,H., Shuldiner,A.R., Siscovick,D.S.,
Stumvoll,M., Tonjes,A., Tuomilehto,J., van Ommen,G.J., Viikari,J.,
Heath,A.C., Martin,N.G., Montgomery,G.W., Province,M.A., Kayser,M.,
Arnold,A.M., Atwood,L.D., Boerwinkle,E., Chanock,S.J., Deloukas,P.,
Gieger,C., Gronberg,H., Hall,P., Hattersley,A.T., Hengstenberg,C.,
Hoffman,W., Lathrop,G.M., Salomaa,V., Schreiber,S., Uda,M.,
Waterworth,D., Wright,A.F., Assimes,T.L., Barroso,I., Hofman,A.,
Mohlke,K.L., Boomsma,D.I., Caulfield,M.J., Cupples,L.A.,
Erdmann,J., Fox,C.S., Gudnason,V., Gyllensten,U., Harris,T.B.,
Hayes,R.B., Jarvelin,M.R., Mooser,V., Munroe,P.B., Ouwehand,W.H.,
Penninx,B.W., Pramstaller,P.P., Quertermous,T., Rudan,I.,
Samani,N.J., Spector,T.D., Volzke,H., Watkins,H., Wilson,J.F.,
Groop,L.C., Haritunians,T., Hu,F.B., Kaplan,R.C., Metspalu,A.,
North,K.E., Schlessinger,D., Wareham,N.J., Hunter,D.J.,
O'Connell,J.R., Strachan,D.P., Wichmann,H.E., Borecki,I.B., van
Duijn,C.M., Schadt,E.E., Thorsteinsdottir,U., Peltonen,L.,
Uitterlinden,A.G., Visscher,P.M., Chatterjee,N., Loos,R.J.,
Boehnke,M., McCarthy,M.I., Ingelsson,E., Lindgren,C.M.,
Abecasis,G.R., Stefansson,K., Frayling,T.M. and Hirschhorn,J.N.
TITLE Hundreds of variants clustered in genomic loci and biological
pathways affect human height
JOURNAL Nature 467 (7317), 832-838 (2010)
PUBMED 20881960
REFERENCE 3 (bases 1 to 7909)
AUTHORS Nilsson,J., Helou,K., Kovacs,A., Bendahl,P.O., Bjursell,G.,
Ferno,M., Carlsson,P. and Kannius-Janson,M.
TITLE Nuclear Janus-activated kinase 2/nuclear factor 1-C2 suppresses
tumorigenesis and epithelial-to-mesenchymal transition by
repressing Forkhead box F1
JOURNAL Cancer Res. 70 (5), 2020-2029 (2010)
PUBMED 20145151
REMARK GeneRIF: novel role of NF1-C2 in tumor development and
epithelial-to-mesenchymal transition in breast cancer; NF1-C2 is
lost during tumor progression and virtully absent from lymph node
metastases; FoxF1 was was found to be a direct repressed target of
NF1-C2
REFERENCE 4 (bases 1 to 7909)
AUTHORS Udelhoven,M., Leeser,U., Freude,S., Hettich,M.M., Laudes,M.,
Schnitker,J., Krone,W. and Schubert,M.
TITLE Identification of a region in the human IRS2 promoter essential for
stress induced transcription depending on SP1, NFI binding and ERK
activation in HepG2 cells
JOURNAL J. Mol. Endocrinol. 44 (2), 99-113 (2010)
PUBMED 19755487
REMARK GeneRIF: A specific region (-688 to -611 bp) was discovered in the
IRS2 promoter essential for basal promoter activity and oxidative
stress induced transcription depending on ERK activation and SP1
and NFI binding in human hepatocytes.
REFERENCE 5 (bases 1 to 7909)
AUTHORS Plasari,G., Calabrese,A., Dusserre,Y., Gronostajski,R.M.,
McNair,A., Michalik,L. and Mermod,N.
TITLE Nuclear factor I-C links platelet-derived growth factor and
transforming growth factor beta1 signaling to skin wound healing
progression
JOURNAL Mol. Cell. Biol. 29 (22), 6006-6017 (2009)
PUBMED 19752192
REMARK GeneRIF: These results imply a central role of NFI-C in the
interplay of the two signaling pathways and in regulation of the
progression of tissue regeneration.
REFERENCE 6 (bases 1 to 7909)
AUTHORS Wenzelides,S., Altmann,H., Wendler,W. and Winnacker,E.L.
TITLE CTF5--a new transcriptional activator of the NFI/CTF family
JOURNAL Nucleic Acids Res. 24 (12), 2416-2421 (1996)
PUBMED 8710515
REFERENCE 7 (bases 1 to 7909)
AUTHORS Blau,J., Xiao,H., McCracken,S., O'Hare,P., Greenblatt,J. and
Bentley,D.
TITLE Three functional classes of transcriptional activation domain
JOURNAL Mol. Cell. Biol. 16 (5), 2044-2055 (1996)
PUBMED 8628270
REFERENCE 8 (bases 1 to 7909)
AUTHORS Qian,F., Kruse,U., Lichter,P. and Sippel,A.E.
TITLE Chromosomal localization of the four genes (NFIA, B, C, and X) for
the human transcription factor nuclear factor I by FISH
JOURNAL Genomics 28 (1), 66-73 (1995)
PUBMED 7590749
REFERENCE 9 (bases 1 to 7909)
AUTHORS Nehls,M.C., Grapilon,M.L. and Brenner,D.A.
TITLE NF-I/Sp1 switch elements regulate collagen alpha 1(I) gene
expression
JOURNAL DNA Cell Biol. 11 (6), 443-452 (1992)
PUBMED 1524678
REFERENCE 10 (bases 1 to 7909)
AUTHORS Santoro,C., Mermod,N., Andrews,P.C. and Tjian,R.
TITLE A family of human CCAAT-box-binding proteins active in
transcription and DNA replication: cloning and expression of
multiple cDNAs
JOURNAL Nature 334 (6179), 218-224 (1988)
PUBMED 3398920
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BF763988.1, BC012120.1,
AK289885.1, CB053896.1, CK431049.1, AC005551.1 and BU727954.1.
Summary: The protein encoded by this gene belongs to the CTF/NF-I
family. These are dimeric DNA-binding proteins, and function as
cellular transcription factors and as replication factors for
adenovirus DNA replication. Alternatively spliced transcript
variants encoding different isoforms have been described for this
gene. [provided by RefSeq, Oct 2011].
Transcript Variant: This variant (3) lacks an exon in the 3' coding
region compared to variant 1. This results in a frame-shift, and a
shorter isoform (3) with a distinct C-terminus compared to isoform
1.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AK297867.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-8 BF763988.1 20-27
9-1339 BC012120.1 1-1331
1340-1983 AK289885.1 1430-2073
1984-2343 CB053896.1 51-410 c
2344-2936 CK431049.1 45-637
2937-7627 AC005551.1 12615-17305
7628-7909 BU727954.1 1-282 c
FEATURES Location/Qualifiers
source 1..7909
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19p13.3"
gene 1..7909
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="nuclear factor I/C (CCAAT-binding transcription
factor)"
/db_xref="GeneID:4782"
/db_xref="HGNC:7786"
/db_xref="MIM:600729"
exon 1..100
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
misc_feature 11..13
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="upstream in-frame stop codon"
variation 46
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:200806100"
variation 52
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:372385803"
variation 62
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:374182689"
CDS 71..1390
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="isoform 3 is encoded by transcript variant 3;
nuclear factor 1 C-type; NF1-C; NF-I/C; TGGCA-binding
protein; CCAAT-box-binding transcription factor"
/codon_start=1
/product="nuclear factor 1 C-type isoform 3"
/protein_id="NP_001231933.1"
/db_xref="GI:350529401"
/db_xref="CCDS:CCDS59331.1"
/db_xref="GeneID:4782"
/db_xref="HGNC:7786"
/db_xref="MIM:600729"
/translation="
MYSSPLCLTQDEFHPFIEALLPHVRAFAYTWFNLQARKRKYFKKHEKRMSKDEERAVKDELLGEKPEVKQKWASRLLAKLRKDIRPECREDFVLSITGKKAPGCVLSNPDQKGKMRRIDCLRQADKVWRLDLVMVILFKGIPLESTDGERLVKAAQCGHPVLCVQPHHIGVAVKELDLYLAYFVRERDAEQSGSPRTGMGSDQEDSKPITLDTTDFQESFVTSGVFSVTELIQVSRTPVVTGTGPNFSLGELQGHLAYDLNPASTGLRRTLPSTSSSGSKRHKSGSMEEDVDTSPGGDYYTSPSSPTSSSRNWTEDMEGGISSPVKKTEMDKSPFNSPSPQDSPRLSSFTQHHRPVIAVHSGIARSPHPSSALHFPTTSILPQTASTYFPHTAIRYPPHLNPQDPLKDLVSLACDPASQQPGPPTLRPTRPLQTVPLWD
"
misc_feature 71..73
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="N-acetylmethionine; propagated from
UniProtKB/Swiss-Prot (P08651.2); acetylation site"
misc_feature 80..211
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="Nuclear factor I protein pre-N-terminus; Region:
NfI_DNAbd_pre-N; pfam10524"
/db_xref="CDD:151076"
misc_feature 272..577
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="N-terminal Mad Homology 1 (MH1) domain; Region:
MH1; cl00055"
/db_xref="CDD:206806"
misc_feature 650..652
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P08651.2); phosphorylation site"
misc_feature 719..>1324
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="CTF/NF-I family transcription modulation region;
Region: CTF_NFI; pfam00859"
/db_xref="CDD:144451"
misc_feature 950..952
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P08651.2); phosphorylation site"
misc_feature 1037..1039
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P08651.2); phosphorylation site"
misc_feature 1067..1069
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P08651.2); phosphorylation site"
misc_feature 1079..1081
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P08651.2); phosphorylation site"
misc_feature 1085..1087
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P08651.2); phosphorylation site"
misc_feature 1097..1099
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P08651.2); phosphorylation site"
exon 101..632
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 131
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:190753458"
variation 151
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:144268546"
variation 178
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:148748813"
variation 180
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:141482719"
variation 190
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370694661"
variation 196
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:150819987"
variation 215
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:139273924"
variation 238
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:201762449"
variation 298
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:144458967"
variation 362
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:146638960"
variation 373
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:367554475"
variation 376
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:369119535"
variation 384
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:61731129"
variation 442
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:199785054"
variation 496
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:146650773"
variation 511
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372862380"
variation 538
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:375768351"
variation 548
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:201434711"
variation 560
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:200551240"
variation 562
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:11878387"
variation 567
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:138699938"
variation 613
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201632995"
variation 619
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372436353"
variation 620
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:201510675"
variation 623
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:369796013"
variation 630
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:201011953"
exon 633..704
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 636
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:145828739"
variation 640
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:369261498"
variation 647
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:200153960"
variation 665
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:78728474"
variation 700
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:371331059"
exon 705..779
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 709
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:377664780"
variation 739
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:111422145"
variation 740
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:143519997"
variation 751
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201124721"
variation 754
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:138225094"
variation 777
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:116865554"
exon 780..903
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 784
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:150930822"
variation 808
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:374471241"
variation 814
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:112569402"
variation 841
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:373306178"
variation 864
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:35952068"
variation 879..880
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:34108601"
variation 885
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:368371894"
exon 904..1028
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 919
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:146070921"
variation 922
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:138945457"
variation 923
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:142790393"
variation 928
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:369569353"
variation 949..950
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/db_xref="dbSNP:34937859"
variation 960
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:373904141"
variation 993
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:200221249"
variation 1012
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:377153122"
variation 1018
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:369185182"
exon 1029..1154
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 1099
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:117114356"
variation 1104
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:200686979"
variation 1132
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:199780384"
variation 1141
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:149374084"
variation 1144
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:375318776"
exon 1155..1339
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 1183
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:138179732"
variation 1221
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:374896582"
variation 1222
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:142781909"
variation 1225
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:201575539"
variation 1234
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:146145775"
variation 1237
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:372361568"
variation 1246
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:200793537"
variation 1254
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:140170107"
variation 1279
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:11671446"
variation 1282
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:142476049"
variation 1285
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:368456734"
variation 1294
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:141932371"
variation 1312
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:1060363"
variation 1319
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:10412720"
variation 1339
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:372367068"
exon 1340..1425
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 1347
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:76459565"
variation 1349
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372572344"
variation 1372
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:376511703"
variation 1415
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:368331116"
exon 1426..7891
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
STS 1433..1558
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH70943"
/db_xref="UniSTS:18913"
variation 1450..1452
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="tct"
/db_xref="dbSNP:202152750"
variation 1492
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:374310905"
variation 1495
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370736060"
variation 1525
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:8047"
variation 1527
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:377580938"
variation 1584
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:62130570"
variation 1616
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:185384063"
variation 1667
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:369618261"
variation 1675
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:143763131"
variation 1753
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:147192339"
variation 1755..1756
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:35103414"
variation 1815
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:112297811"
variation 1867
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:371877071"
variation 2152
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:35033094"
variation 2208
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:189392307"
variation 2218
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:376897288"
variation 2441
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:115020939"
variation 2444
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:4807474"
variation 2578
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:116669109"
variation 2704
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373175985"
variation 2724
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:74656266"
variation 2749..2750
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:143359349"
variation 2849
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:10426917"
variation 2917
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:10426352"
variation 2964
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:140546305"
variation 2996
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:3746298"
variation 2997
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:3746299"
variation 3015
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:7258954"
variation 3172
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:115534300"
variation 3199
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:6510757"
variation 3375
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:191016688"
variation 3388
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:12971613"
variation 3469
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:142170418"
variation 3650
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:11673590"
STS 3664..3795
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH47688"
/db_xref="UniSTS:41852"
variation 3694
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:60093027"
variation 3794
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:713043"
variation 3798
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:11666623"
variation 3811
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:61089125"
variation 3826..3827
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:71782480"
variation 3837
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaaa"
/db_xref="dbSNP:71708589"
variation 3848..3849
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:59668846"
variation 3849..3853
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="gatac"
/db_xref="dbSNP:146468333"
variation 3849
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201570343"
variation 3851
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:369702439"
variation 3852
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:2392709"
variation 3853
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373239554"
variation 3856
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:377659423"
variation 3904
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:56294037"
variation 3998
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:11541514"
variation 4072..4076
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaat"
/db_xref="dbSNP:142281202"
variation 4076
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:370549069"
variation 4081
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaat"
/db_xref="dbSNP:71731809"
variation 4081
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:373766499"
variation 4088
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:377329843"
variation 4091
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370429651"
variation 4116
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:10617203"
variation 4129..4130
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="gg"
/db_xref="dbSNP:373260051"
variation 4356
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:150732039"
variation 4362
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:112962670"
variation 4373
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:190974806"
variation 4440
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:112077871"
variation 4458
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370523643"
variation 4503
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373678102"
variation 4554
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:371834921"
variation 4566
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:139103336"
variation 4747
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:116639605"
variation 4897..4898
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:11388112"
variation 4897
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201353930"
variation 4904..4905
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:200434679"
variation 4909
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:375507336"
variation 5068
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:182718334"
variation 5112
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:376532943"
variation 5146
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:149869150"
variation 5273
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:188692410"
variation 5284
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:191740254"
variation 5287
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:111606883"
variation 5332..5333
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:112243853"
variation 5368
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:73919194"
variation 5394
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:183256663"
variation 5427
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:368229276"
variation 5487
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:202195970"
variation 5534
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:373841623"
STS 5662..5822
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="A008X33"
/db_xref="UniSTS:11659"
variation 5710
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:148735510"
variation 5739
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:188079746"
variation 5769..5770
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:201187022"
variation 5775
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8112889"
variation 5776..5777
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:146782728"
variation 5776
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8108753"
variation 5777..5778
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:68098094"
variation 5779..5780
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:373716537"
variation 5782
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:148147968"
variation 5782
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8108755"
variation 5789..5790
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:59410286"
variation 5815
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:182356784"
variation 5887
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:374469121"
variation 5897
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="c"
/db_xref="dbSNP:11357750"
variation 5929
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:118139977"
variation 5980
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:187795070"
variation 5983
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:111969590"
variation 6134
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:192533268"
variation 6296
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:146433383"
variation 6383
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:73919195"
STS 6407..6543
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="G32369"
/db_xref="UniSTS:116958"
STS 6407..6543
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH67057"
/db_xref="UniSTS:84684"
variation 6432..6433
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatatat"
/db_xref="dbSNP:374523932"
variation 6432..6433
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:8110278"
variation 6432
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:28665162"
variation 6433..6452
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatat"
/db_xref="dbSNP:375414685"
variation 6433..6434
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatatat"
/replace="atatattatatatatatatat"
/db_xref="dbSNP:34605422"
variation 6440
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:185019123"
variation 6455
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:190207945"
variation 6465..6466
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:35325992"
variation 6498
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:8113786"
variation 6536
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:192998513"
variation 6568
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:116148466"
variation 6608
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:72974787"
variation 6641
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:140704632"
variation 6666
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:8110928"
variation 6682
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372237245"
variation 6864..6865
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:377115512"
variation 6869
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:374793831"
variation 6872
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:369655483"
variation 7000
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:184806177"
variation 7127
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:74741143"
variation 7179
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:4807475"
variation 7260
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:188683808"
variation 7289
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:376460082"
variation 7329
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:144557238"
variation 7388..7389
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:199586457"
variation 7439..7441
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="ctt"
/db_xref="dbSNP:370673109"
variation 7441..7443
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="tct"
/db_xref="dbSNP:57761031"
variation 7451
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:180737599"
variation 7514
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:185090028"
variation 7614
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:369940873"
variation 7638
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:146638802"
STS 7641..7768
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="WI-12079"
/db_xref="UniSTS:15156"
variation 7645
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:35160631"
STS 7656..7772
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH36034"
/db_xref="UniSTS:47850"
variation 7659
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:189164209"
variation 7678
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:10417031"
variation 7731
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:141326218"
variation 7754
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:11547206"
variation 7826..7829
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="acaa"
/db_xref="dbSNP:199877074"
variation 7828..7832
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaca"
/db_xref="dbSNP:147791651"
variation 7828
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaca"
/db_xref="dbSNP:71715433"
variation 7831..7835
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:146550572"
variation 7831
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:10543929"
variation 7831
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:60861688"
variation 7835
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:373990617"
variation 7836..7837
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="ag"
/db_xref="dbSNP:71656643"
variation 7837
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:12983451"
polyA_signal 7866..7871
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
polyA_site 7891
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
ORIGIN
tttggaaaaatgactcagtaagttcagcgcgcccgctccggccggccctgcgcctcccgccgcgcccgggatgtattcgtccccgctctgcctcacccaggatgagttccacccgttcatcgaggccctgctgcctcacgtccgcgccttcgcctacacctggttcaacctgcaggcgcggaagcgcaagtacttcaagaagcacgagaagcggatgtcgaaggacgaggagcgtgcggtcaaggacgagctgctgggcgagaagcccgaggtcaagcagaagtgggcgtcgcggctgctggccaagctgcgcaaggacatccggcccgagtgccgcgaggacttcgtgctgagcatcaccggcaagaaggcgccgggctgcgtgctctccaaccccgaccagaagggcaagatgcggcgcatcgactgtctccggcaggcggacaaggtgtggcggctggacctggtcatggtcatcctgttcaagggcatcccgctggagagcaccgacggcgagcgcctggtcaaggctgcgcagtgcggtcacccggtcctgtgcgtgcagccgcaccacattggcgtggccgtcaaggagctggacctctacctggcctacttcgtgcgtgagcgagatgcagagcaaagcggcagtccccggacagggatgggctctgaccaggaggacagcaagcccatcacgctggacacgaccgacttccaggagagctttgtcacctccggcgtgttcagcgtcactgagctcatccaagtgtcccggacacccgtggtgactggaacaggacccaacttctccctgggggagctgcaggggcacctggcatacgacctgaacccagccagcactggcctcagaagaacgctgcccagcacctcctccagtgggagcaagcggcacaaatcgggctcgatggaggaagacgtggacacgagccctggcggcgattactacacttcgcccagctcgcccacgagtagcagccgcaactggacggaggacatggaaggaggcatctcgtccccggtgaagaagacagagatggacaagtcaccattcaacagcccgtccccccaggactctccccgcctctccagcttcacccagcaccaccggcccgtcatcgccgtgcacagcgggatcgcccggagcccacacccgtcctccgctctgcatttccctacgacgtccatcctaccccagacggcctccacctacttcccccacacggccatccgctacccacctcatctcaacccccaggacccgctcaaagatcttgtctcgctggcctgcgacccagccagccagcaacctggaccgcctactctccgcccgacacgtcccctgcaaaccgttcctttgtgggattaggaccaagggatcctgcgggcatttatcaggcacagtcctggtatctgggatagcaaaggtcttcttccctcgccccttctccatcgtcccaggaatcccagggggcagcacagccggcccccggcccacgttttcggtggaaaattagagtgaacaagaacacccctgccgactcccagcccggccaaaaagacaaaacacatagacgcacacactcaggaggaaaagaaaaaacaaaggcagaagaagaagaagaagaaataaaaacccacccaagcaagaagacaaaaggtaaagacgcaacgtttccaactctcgggacgccaaggccgcaggactggagggccaggccccgccacccccacgggagacccgggacagggcgtcttcctaagttattcatctcctctccgcctgctgctcgggaaggacagacgccggccgcccgcccgcgccccggaggccctggctctgtccggagaccaggtgagcacagcctggagcctgtgcccagggccgacaggcgcgacacccagcaaggccacctctccccgggcccccgcgcctctgccggacacggaccggcccctcagcccccaccgaggacgcagccactggggggaaagggagacacagcggaccccggccgggcagcggagaccgcagaggcgggcagggtggggcaggcgagtggtgtcgcgggggtgcgtggcgcttgcgagccctggccaggggaggaagtgaggcccaggcacctgctgcccctcgagggggccctgcctgccgcggggcctccccacaagcccctcccaaagcgccggccgactcgctgtctcgctggggactctttcagccctcgcgcccgcccgtttgggaggagaagtctctatgcaattggccccggcccctccaccccccacccccggcataggaggcccccccacctcgcccggctcacacccccaaagggagggacccacattgcacacactgtaagaaatgcactttccgaggaaggggatgggggagcccggacacccagagctccccgagttgggggtgcccgtctggagcgcccccgtcagcccctggcggtgggaggtgagagcgagtggtttaagtgcctgattaccaccacccgcccccccctttgtccagctgggacacggaatggccgcgggcctcctccccctcccctccagcctctccaccagcccctccagtcaaccctcatcgccgtgcccccccagagctagagagatggggcccctgcgtggcccgaggggcagagctgggcgtcacttcgcaagcgtcctgccctgccggggcgcgggggtgggctctggggaagccggtgcgccccccacgcctccgctgccagtgccttacattctggagcgacccccctccctggtgcctcccagcgaagggggaccgccgtttgcactttcatcgcctaccccgacgcggggcccagctgcgggacgtgcatcacggctgggcccccagaggagagaggaggccgacgccagcggtccccgctcggaacggggagggttttcggggggttcggcgtcgcaccttggggccccccgcagccgtgtagggggcctcccatctgctaagcgtttttccgttgagccgctccaaaaacactaagctggggacgccaggtgcccccccaccccggctccctggccctatccacacctccacccccaccccaggatcgccatctttaggggaggcctgggagggggtgttaggtgttttagggccaccgagctcaaacacaaggacccctccccggcccacccagcccagccccaactgacctccatgcctagggaaaaactccccccaccactgccccctcccccgacccaggccaaagccagggcaggtctccgggtctcacctgctcctagcctcacccccctgcccccgaaaaccagactctcctcccaaactagcctcaggagcttggcgaacccgctcgctcctaaagagaaagacccaggaccctcccccatcacccccaagagaggttcgccatcctctggcctcgagcccttggtccctccgtccgtctgtcctcggggcccgctcccccggtggcccttggggatcaaagcgtgggccgctctccgggagggcgggcgggggagggggtggtcgggttgtgccattggggtgtccggaagcttctcagccagggtgggggtcgtggagtgggggagggaggccagccgggctccagaggggtcagggcgcgacgagaaccaactctttacctaactttgcatggtgcttagtcaaggactcctgcgacctggctcccgaggtcagctggcggcgctgacacacatgcatggcagactatccctggctctatctccctgttcctcgccccctccaccccccacttcctctttaaaaaaaaaaaaaaaaaaaaaaagatacaagaaaaacctttaaaaaaattccatgtttcctaatttgcacgaaattttctaccacaagatgtgccttgccttccgagaataagtattacctttaaacaatatcagcgcacacacatagctgcatgttctgctcgtgtagtttaaaaaaaaaaagacaaaacagtgacatgaaataaaaaataaaaattgaaaagggatgtatttctatttgtaaaaaaaataaaataaaaaataagaaagtgagaatctaaaaaaaaaaaaaaaaaaaaaaaaggaagaaaaaccacgctaaaaatcaagccactgaaaacaattgcccccaggtctacccagcccctggctgtccttggtcctgtctcccctcctgctgtattcaggggtgccccctggtgctcagcctctaccacccccaaccctgctcttgggtacccagaggggtcatttctgaatcccttgcccagaggacagacctccggggcccatcttggccctgggaaagggctctcctctctgattggtccctaggccacgggccggcccccagacaccattcaccgacccactgcaggctgtcctccaaccatggggtggccactccacccgcagccagactccccgctccccacttttcatgcaggctggcatacccctggctcagggtcaaatgctgttccacacccacctcagaggcaccccctctcccctgccccgtgcatccccacccttcttgccaaaggacctcttttcccctatccagagaccaccccaggtggcattctctcccaccttctcctttgtcccccatcccctgtctctgtcttccagctgtgaatatgaagggtatcctgtatgaaacaaaaacaaaacctgatatatgcaatatctgtctgtctgtctgtacccatgggcctggctcagccattggaggcccagccgagggtccggcagggcacagggacagccaggtggcaccgagtcacaggctgtggtccggtggctgagcatgctgttgtcttgtccttgattttattttcttttgttctttttttttttcttttctttttgtttttaactccagcttcctttgctttttacttgaccaaagctaagacaatagccagatggttagtggggcagccaggcagggaggacccagggctgggattctccaaccttaggccattcctgcagccctcaccacctccagcccctccaagcatctcgtgtagggacccacgcagatggtcccattcattcactattgcccccaaccccgggattttgggtggtctccacagccaccatcatacactcatcccgtgttttcttccaaaaagtcacctcagcagcctccccaggcgatacagagggagagcccagaccaccacagctggccacgacattgcccttaagtaatatgcattggccagagagcccgggctggctgtgcacagcattcatgtagctgatttctagctttttttttttttctgccccactcctgagcaaatctgtcttgccaaggaactaggagcaaccggaggcaaagggagtgggtggccccatcactattgggaccatcgcgtccctgcacagcccacacccgggggcccagagtcctgggctggacgccacccttctcaccccgagcttgcctccttggctcacttggcaccttggctgagtacagcaggcaaaagcccataccaggcagcatgttgtggatggtttagttctccccgcctccctgtttcttggaaaagctacagggtccctgtagggcaaaattcccaggcgccttgctgcagacagagtaagacaaaaacaccaggaagcaggattccgtgcccatctctgcagtttgggttcacaaaagggggtgccgtcatccctgggtggaggagggagtgttggttttttgtttttgtttttttaacatgtatgaaactgacatcttctcaaatcttgttccacccccctctggaagcccccatcacccacccctgctatggacaccacacctatgccaggcccccccccccaccccagtctcattctggggtctgcccatgctgtgggaaagaatagggaggcctcccaaatatatgcaaattgtccccattccgtgggggcacctgacaatgacccgggtggagatggggcatggaggagtaggaagacccagccctatttgactggggagaggaggatctggagtccttcatgcccaggtctggaacccaggttctgaccccagggccccaccctgggctggacaatcagatcccaaaggaatgccaaaggggactcggttgggagagccgcttaggggccagacctgggtccccctgcaggtccccaggcagcagacaattccaccttccctgccccaggaccttgagagacagcagcattccaggcacagacagacttggctgcaccccactgtcccttgcaagacaggttctggagccaggagcaactgtccagccctccagaagagacagcaagcagcccccctacccactctggcctccccaatggtactttgacctccagtgtagggctatactatacatatatatatatatatatatatatatatataattttggaatttgtttctcataatacagaatatatagtggctaccttgtatcttggtctggattctctctctgagaccccggattttactttctctttggagggcgctgggacatacatctctcaatccagcttcctccgcatcctcccatcttgccccatttctgccacgtcagacacttcctgagagtctcaccttcaaaatgacaccgctgcccatccattgctcaatggtacagagtgtggggtcagtccaccacccttgacctcccggcagggcaaggtgaggaggcggacccaaagcagtaccagcaggacttgttgccagtgataccaaaacagacttttcccaagcagtgcctcacatgtctgctggtgtggctttgggattctcctgccccacccccccgtccatggcagccccctccccaaggctttgctcacacctgagacaggaaggaggaaggggatccaataggaatatgggccccggaggggaagtcatgcacccccaagccaccaccccccagccttccacgcacatctcctggctggaagagagccctccaaaaaggggacacaggctgccccggcccctcaactgcatccacaccccatcctctcatcttgggtcccagccaggcccccccaaaaccaaagccccctcaagtcctggggtcccagcctgtgcccccagcttcctgcccacccagccctgagcattctcacacagagaaagaacaagcaagggctccagggggacaggatggggcagggcatacagtggggggtgggggggcagctgggaggagggagggacaaaacaaaacattttcctttgggttttttttttctttcttttttctcccctttactctttgggtggtgttgcttttcctttccttttccctttgagatttttttgttgttgtttcctttttgtattttactgatatcaccaggatagtttactctccttctagctttctgcttaccgcacactggataacacacacatacacacccacaaaaatgctcatgaacccaatccggagaaggttccagcaggtcccccaccctcccctcctcctcctacttctcctcttgacagcgaggacaggagggggacaaggggacacctgggcagacccgccggctctccccccaccccaccccgcccctcacatcatactccaatcataaccttgtatattacgcagtcattttggttttcgcggacgcgcctacctaagtaccatttacagaaagtgactctggctgtcattattttgtttatttgttccctatgcaaaaaaaaaatgaaaatgaaaaaagggggattccataaaagattcaataaaagacaaacaaaaaaaaaagaaaaaagaaaaaaatgtataaaaattaaacaagctatgcttcgactcttaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS 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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