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2024-04-19 15:42:36, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_005597 7823 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens nuclear factor I/C (CCAAT-binding transcription
factor) (NFIC), transcript variant 5, mRNA.
ACCESSION NM_005597
VERSION NM_005597.3 GI:350529399
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 7823)
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 7823)
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 7823)
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 7823)
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 7823)
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 7823)
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 7823)
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 7823)
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 7823)
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 7823)
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.
On Oct 8, 2011 this sequence version replaced gi:45505148.
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 (5) lacks two consecutive in-frame
coding exons compared to variant 1. This results in a shorter
isoform (5) missing an internal protein segment 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 :: BC012120.1, X92857.1 [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
9-1555 BC012120.1 1-1547
1556-1897 AK289885.1 1732-2073
1898-2257 CB053896.1 51-410 c
2258-2850 CK431049.1 45-637
2851-7541 AC005551.1 12615-17305
7542-7823 BU727954.1 1-282 c
FEATURES Location/Qualifiers
source 1..7823
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19p13.3"
gene 1..7823
/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..1357
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="isoform 5 is encoded by transcript variant 5;
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 5"
/protein_id="NP_005588.2"
/db_xref="GI:45505149"
/db_xref="CCDS:CCDS12107.1"
/db_xref="GeneID:4782"
/db_xref="HGNC:7786"
/db_xref="MIM:600729"
/translation="
MYSSPLCLTQDEFHPFIEALLPHVRAFAYTWFNLQARKRKYFKKHEKRMSKDEERAVKDELLGEKPEVKQKWASRLLAKLRKDIRPECREDFVLSITGKKAPGCVLSNPDQKGKMRRIDCLRQADKVWRLDLVMVILFKGIPLESTDGERLVKAAQCGHPVLCVQPHHIGVAVKELDLYLAYFVRERDAEQSGSPRTGMGSDQEDSKPITLDTTDFQESFVTSGVFSVTELIQVSRTPVVTGTGPNFSLGELQGHLAYDLNPASTGLRRTLPSTSSSGSKRHKSGSMEEDVDTSPGGDYYTSPSSPTSSSRNWTEDMEGGISSPVKKTEMDKSPFNSPSPQDSPRLSSFTQHHRPVIAVHSGIARSPHPSSALHFPTTSILPQTASTYFPHTAIRYPPHLNPQDPLKDLVSLACDPASQQPGPSWYLG
"
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 80..82
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
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 644..646
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
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 650..652
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 719..>1339
/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 1037..1039
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="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 1067..1069
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="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 1079..1081
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="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 1085..1087
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1085..1087
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="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..7805
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
STS 1347..1472
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH70943"
/db_xref="UniSTS:18913"
variation 1364..1366
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="tct"
/db_xref="dbSNP:202152750"
variation 1406
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:374310905"
variation 1409
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370736060"
variation 1439
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:8047"
variation 1441
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:377580938"
variation 1498
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:62130570"
variation 1530
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:185384063"
variation 1581
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:369618261"
variation 1589
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:143763131"
variation 1667
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:147192339"
variation 1669..1670
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:35103414"
variation 1729
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:112297811"
variation 1781
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:371877071"
variation 2066
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:35033094"
variation 2122
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:189392307"
variation 2132
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:376897288"
variation 2355
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:115020939"
variation 2358
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:4807474"
variation 2492
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:116669109"
variation 2618
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373175985"
variation 2638
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:74656266"
variation 2663..2664
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:143359349"
variation 2763
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:10426917"
variation 2831
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:10426352"
variation 2878
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:140546305"
variation 2910
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:3746298"
variation 2911
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:3746299"
variation 2929
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:7258954"
variation 3086
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:115534300"
variation 3113
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:6510757"
variation 3289
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:191016688"
variation 3302
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:12971613"
variation 3383
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:142170418"
variation 3564
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:11673590"
STS 3578..3709
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH47688"
/db_xref="UniSTS:41852"
variation 3608
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:60093027"
variation 3708
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:713043"
variation 3712
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:11666623"
variation 3725
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:61089125"
variation 3740..3741
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:71782480"
variation 3751
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaaa"
/db_xref="dbSNP:71708589"
variation 3762..3763
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:59668846"
variation 3763..3767
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="gatac"
/db_xref="dbSNP:146468333"
variation 3763
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201570343"
variation 3765
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:369702439"
variation 3766
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:2392709"
variation 3767
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373239554"
variation 3770
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:377659423"
variation 3818
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:56294037"
variation 3912
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:11541514"
variation 3986..3990
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaat"
/db_xref="dbSNP:142281202"
variation 3990
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:370549069"
variation 3995
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaat"
/db_xref="dbSNP:71731809"
variation 3995
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:373766499"
variation 4002
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:377329843"
variation 4005
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370429651"
variation 4030
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:10617203"
variation 4043..4044
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="gg"
/db_xref="dbSNP:373260051"
variation 4270
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:150732039"
variation 4276
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:112962670"
variation 4287
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:190974806"
variation 4354
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:112077871"
variation 4372
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370523643"
variation 4417
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373678102"
variation 4468
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:371834921"
variation 4480
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:139103336"
variation 4661
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:116639605"
variation 4811..4812
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:11388112"
variation 4811
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201353930"
variation 4818..4819
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:200434679"
variation 4823
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:375507336"
variation 4982
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:182718334"
variation 5026
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:376532943"
variation 5060
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:149869150"
variation 5187
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:188692410"
variation 5198
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:191740254"
variation 5201
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:111606883"
variation 5246..5247
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:112243853"
variation 5282
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:73919194"
variation 5308
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:183256663"
variation 5341
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:368229276"
variation 5401
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:202195970"
variation 5448
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:373841623"
STS 5576..5736
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="A008X33"
/db_xref="UniSTS:11659"
variation 5624
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:148735510"
variation 5653
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:188079746"
variation 5683..5684
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:201187022"
variation 5689
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8112889"
variation 5690..5691
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:146782728"
variation 5690
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8108753"
variation 5691..5692
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:68098094"
variation 5693..5694
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:373716537"
variation 5696
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:148147968"
variation 5696
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8108755"
variation 5703..5704
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:59410286"
variation 5729
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:182356784"
variation 5801
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:374469121"
variation 5811
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="c"
/db_xref="dbSNP:11357750"
variation 5843
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:118139977"
variation 5894
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:187795070"
variation 5897
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:111969590"
variation 6048
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:192533268"
variation 6210
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:146433383"
variation 6297
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:73919195"
STS 6321..6457
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="G32369"
/db_xref="UniSTS:116958"
STS 6321..6457
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH67057"
/db_xref="UniSTS:84684"
variation 6346..6347
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatatat"
/db_xref="dbSNP:374523932"
variation 6346..6347
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:8110278"
variation 6346
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:28665162"
variation 6347..6366
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatat"
/db_xref="dbSNP:375414685"
variation 6347..6348
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatatat"
/replace="atatattatatatatatatat"
/db_xref="dbSNP:34605422"
variation 6354
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:185019123"
variation 6369
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:190207945"
variation 6379..6380
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:35325992"
variation 6412
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:8113786"
variation 6450
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:192998513"
variation 6482
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:116148466"
variation 6522
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:72974787"
variation 6555
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:140704632"
variation 6580
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:8110928"
variation 6596
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372237245"
variation 6778..6779
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:377115512"
variation 6783
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:374793831"
variation 6786
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:369655483"
variation 6914
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:184806177"
variation 7041
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:74741143"
variation 7093
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:4807475"
variation 7174
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:188683808"
variation 7203
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:376460082"
variation 7243
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:144557238"
variation 7302..7303
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:199586457"
variation 7353..7355
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="ctt"
/db_xref="dbSNP:370673109"
variation 7355..7357
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="tct"
/db_xref="dbSNP:57761031"
variation 7365
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:180737599"
variation 7428
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:185090028"
variation 7528
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:369940873"
variation 7552
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:146638802"
STS 7555..7682
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="WI-12079"
/db_xref="UniSTS:15156"
variation 7559
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:35160631"
STS 7570..7686
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH36034"
/db_xref="UniSTS:47850"
variation 7573
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:189164209"
variation 7592
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:10417031"
variation 7645
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:141326218"
variation 7668
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:11547206"
variation 7740..7743
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="acaa"
/db_xref="dbSNP:199877074"
variation 7742..7746
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaca"
/db_xref="dbSNP:147791651"
variation 7742
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaca"
/db_xref="dbSNP:71715433"
variation 7745..7749
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:146550572"
variation 7745
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:10543929"
variation 7745
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:60861688"
variation 7749
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:373990617"
variation 7750..7751
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="ag"
/db_xref="dbSNP:71656643"
variation 7751
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:12983451"
polyA_signal 7780..7785
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
polyA_site 7805
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
ORIGIN
tttggaaaaatgactcagtaagttcagcgcgcccgctccggccggccctgcgcctcccgccgcgcccgggatgtattcgtccccgctctgcctcacccaggatgagttccacccgttcatcgaggccctgctgcctcacgtccgcgccttcgcctacacctggttcaacctgcaggcgcggaagcgcaagtacttcaagaagcacgagaagcggatgtcgaaggacgaggagcgtgcggtcaaggacgagctgctgggcgagaagcccgaggtcaagcagaagtgggcgtcgcggctgctggccaagctgcgcaaggacatccggcccgagtgccgcgaggacttcgtgctgagcatcaccggcaagaaggcgccgggctgcgtgctctccaaccccgaccagaagggcaagatgcggcgcatcgactgtctccggcaggcggacaaggtgtggcggctggacctggtcatggtcatcctgttcaagggcatcccgctggagagcaccgacggcgagcgcctggtcaaggctgcgcagtgcggtcacccggtcctgtgcgtgcagccgcaccacattggcgtggccgtcaaggagctggacctctacctggcctacttcgtgcgtgagcgagatgcagagcaaagcggcagtccccggacagggatgggctctgaccaggaggacagcaagcccatcacgctggacacgaccgacttccaggagagctttgtcacctccggcgtgttcagcgtcactgagctcatccaagtgtcccggacacccgtggtgactggaacaggacccaacttctccctgggggagctgcaggggcacctggcatacgacctgaacccagccagcactggcctcagaagaacgctgcccagcacctcctccagtgggagcaagcggcacaaatcgggctcgatggaggaagacgtggacacgagccctggcggcgattactacacttcgcccagctcgcccacgagtagcagccgcaactggacggaggacatggaaggaggcatctcgtccccggtgaagaagacagagatggacaagtcaccattcaacagcccgtccccccaggactctccccgcctctccagcttcacccagcaccaccggcccgtcatcgccgtgcacagcgggatcgcccggagcccacacccgtcctccgctctgcatttccctacgacgtccatcctaccccagacggcctccacctacttcccccacacggccatccgctacccacctcatctcaacccccaggacccgctcaaagatcttgtctcgctggcctgcgacccagccagccagcaacctggaccgtcctggtatctgggatagcaaaggtcttcttccctcgccccttctccatcgtcccaggaatcccagggggcagcacagccggcccccggcccacgttttcggtggaaaattagagtgaacaagaacacccctgccgactcccagcccggccaaaaagacaaaacacatagacgcacacactcaggaggaaaagaaaaaacaaaggcagaagaagaagaagaagaaataaaaacccacccaagcaagaagacaaaaggtaaagacgcaacgtttccaactctcgggacgccaaggccgcaggactggagggccaggccccgccacccccacgggagacccgggacagggcgtcttcctaagttattcatctcctctccgcctgctgctcgggaaggacagacgccggccgcccgcccgcgccccggaggccctggctctgtccggagaccaggtgagcacagcctggagcctgtgcccagggccgacaggcgcgacacccagcaaggccacctctccccgggcccccgcgcctctgccggacacggaccggcccctcagcccccaccgaggacgcagccactggggggaaagggagacacagcggaccccggccgggcagcggagaccgcagaggcgggcagggtggggcaggcgagtggtgtcgcgggggtgcgtggcgcttgcgagccctggccaggggaggaagtgaggcccaggcacctgctgcccctcgagggggccctgcctgccgcggggcctccccacaagcccctcccaaagcgccggccgactcgctgtctcgctggggactctttcagccctcgcgcccgcccgtttgggaggagaagtctctatgcaattggccccggcccctccaccccccacccccggcataggaggcccccccacctcgcccggctcacacccccaaagggagggacccacattgcacacactgtaagaaatgcactttccgaggaaggggatgggggagcccggacacccagagctccccgagttgggggtgcccgtctggagcgcccccgtcagcccctggcggtgggaggtgagagcgagtggtttaagtgcctgattaccaccacccgcccccccctttgtccagctgggacacggaatggccgcgggcctcctccccctcccctccagcctctccaccagcccctccagtcaaccctcatcgccgtgcccccccagagctagagagatggggcccctgcgtggcccgaggggcagagctgggcgtcacttcgcaagcgtcctgccctgccggggcgcgggggtgggctctggggaagccggtgcgccccccacgcctccgctgccagtgccttacattctggagcgacccccctccctggtgcctcccagcgaagggggaccgccgtttgcactttcatcgcctaccccgacgcggggcccagctgcgggacgtgcatcacggctgggcccccagaggagagaggaggccgacgccagcggtccccgctcggaacggggagggttttcggggggttcggcgtcgcaccttggggccccccgcagccgtgtagggggcctcccatctgctaagcgtttttccgttgagccgctccaaaaacactaagctggggacgccaggtgcccccccaccccggctccctggccctatccacacctccacccccaccccaggatcgccatctttaggggaggcctgggagggggtgttaggtgttttagggccaccgagctcaaacacaaggacccctccccggcccacccagcccagccccaactgacctccatgcctagggaaaaactccccccaccactgccccctcccccgacccaggccaaagccagggcaggtctccgggtctcacctgctcctagcctcacccccctgcccccgaaaaccagactctcctcccaaactagcctcaggagcttggcgaacccgctcgctcctaaagagaaagacccaggaccctcccccatcacccccaagagaggttcgccatcctctggcctcgagcccttggtccctccgtccgtctgtcctcggggcccgctcccccggtggcccttggggatcaaagcgtgggccgctctccgggagggcgggcgggggagggggtggtcgggttgtgccattggggtgtccggaagcttctcagccagggtgggggtcgtggagtgggggagggaggccagccgggctccagaggggtcagggcgcgacgagaaccaactctttacctaactttgcatggtgcttagtcaaggactcctgcgacctggctcccgaggtcagctggcggcgctgacacacatgcatggcagactatccctggctctatctccctgttcctcgccccctccaccccccacttcctctttaaaaaaaaaaaaaaaaaaaaaaagatacaagaaaaacctttaaaaaaattccatgtttcctaatttgcacgaaattttctaccacaagatgtgccttgccttccgagaataagtattacctttaaacaatatcagcgcacacacatagctgcatgttctgctcgtgtagtttaaaaaaaaaaagacaaaacagtgacatgaaataaaaaataaaaattgaaaagggatgtatttctatttgtaaaaaaaataaaataaaaaataagaaagtgagaatctaaaaaaaaaaaaaaaaaaaaaaaaggaagaaaaaccacgctaaaaatcaagccactgaaaacaattgcccccaggtctacccagcccctggctgtccttggtcctgtctcccctcctgctgtattcaggggtgccccctggtgctcagcctctaccacccccaaccctgctcttgggtacccagaggggtcatttctgaatcccttgcccagaggacagacctccggggcccatcttggccctgggaaagggctctcctctctgattggtccctaggccacgggccggcccccagacaccattcaccgacccactgcaggctgtcctccaaccatggggtggccactccacccgcagccagactccccgctccccacttttcatgcaggctggcatacccctggctcagggtcaaatgctgttccacacccacctcagaggcaccccctctcccctgccccgtgcatccccacccttcttgccaaaggacctcttttcccctatccagagaccaccccaggtggcattctctcccaccttctcctttgtcccccatcccctgtctctgtcttccagctgtgaatatgaagggtatcctgtatgaaacaaaaacaaaacctgatatatgcaatatctgtctgtctgtctgtacccatgggcctggctcagccattggaggcccagccgagggtccggcagggcacagggacagccaggtggcaccgagtcacaggctgtggtccggtggctgagcatgctgttgtcttgtccttgattttattttcttttgttctttttttttttcttttctttttgtttttaactccagcttcctttgctttttacttgaccaaagctaagacaatagccagatggttagtggggcagccaggcagggaggacccagggctgggattctccaaccttaggccattcctgcagccctcaccacctccagcccctccaagcatctcgtgtagggacccacgcagatggtcccattcattcactattgcccccaaccccgggattttgggtggtctccacagccaccatcatacactcatcccgtgttttcttccaaaaagtcacctcagcagcctccccaggcgatacagagggagagcccagaccaccacagctggccacgacattgcccttaagtaatatgcattggccagagagcccgggctggctgtgcacagcattcatgtagctgatttctagctttttttttttttctgccccactcctgagcaaatctgtcttgccaaggaactaggagcaaccggaggcaaagggagtgggtggccccatcactattgggaccatcgcgtccctgcacagcccacacccgggggcccagagtcctgggctggacgccacccttctcaccccgagcttgcctccttggctcacttggcaccttggctgagtacagcaggcaaaagcccataccaggcagcatgttgtggatggtttagttctccccgcctccctgtttcttggaaaagctacagggtccctgtagggcaaaattcccaggcgccttgctgcagacagagtaagacaaaaacaccaggaagcaggattccgtgcccatctctgcagtttgggttcacaaaagggggtgccgtcatccctgggtggaggagggagtgttggttttttgtttttgtttttttaacatgtatgaaactgacatcttctcaaatcttgttccacccccctctggaagcccccatcacccacccctgctatggacaccacacctatgccaggcccccccccccaccccagtctcattctggggtctgcccatgctgtgggaaagaatagggaggcctcccaaatatatgcaaattgtccccattccgtgggggcacctgacaatgacccgggtggagatggggcatggaggagtaggaagacccagccctatttgactggggagaggaggatctggagtccttcatgcccaggtctggaacccaggttctgaccccagggccccaccctgggctggacaatcagatcccaaaggaatgccaaaggggactcggttgggagagccgcttaggggccagacctgggtccccctgcaggtccccaggcagcagacaattccaccttccctgccccaggaccttgagagacagcagcattccaggcacagacagacttggctgcaccccactgtcccttgcaagacaggttctggagccaggagcaactgtccagccctccagaagagacagcaagcagcccccctacccactctggcctccccaatggtactttgacctccagtgtagggctatactatacatatatatatatatatatatatatatatataattttggaatttgtttctcataatacagaatatatagtggctaccttgtatcttggtctggattctctctctgagaccccggattttactttctctttggagggcgctgggacatacatctctcaatccagcttcctccgcatcctcccatcttgccccatttctgccacgtcagacacttcctgagagtctcaccttcaaaatgacaccgctgcccatccattgctcaatggtacagagtgtggggtcagtccaccacccttgacctcccggcagggcaaggtgaggaggcggacccaaagcagtaccagcaggacttgttgccagtgataccaaaacagacttttcccaagcagtgcctcacatgtctgctggtgtggctttgggattctcctgccccacccccccgtccatggcagccccctccccaaggctttgctcacacctgagacaggaaggaggaaggggatccaataggaatatgggccccggaggggaagtcatgcacccccaagccaccaccccccagccttccacgcacatctcctggctggaagagagccctccaaaaaggggacacaggctgccccggcccctcaactgcatccacaccccatcctctcatcttgggtcccagccaggcccccccaaaaccaaagccccctcaagtcctggggtcccagcctgtgcccccagcttcctgcccacccagccctgagcattctcacacagagaaagaacaagcaagggctccagggggacaggatggggcagggcatacagtggggggtgggggggcagctgggaggagggagggacaaaacaaaacattttcctttgggttttttttttctttcttttttctcccctttactctttgggtggtgttgcttttcctttccttttccctttgagatttttttgttgttgtttcctttttgtattttactgatatcaccaggatagtttactctccttctagctttctgcttaccgcacactggataacacacacatacacacccacaaaaatgctcatgaacccaatccggagaaggttccagcaggtcccccaccctcccctcctcctcctacttctcctcttgacagcgaggacaggagggggacaaggggacacctgggcagacccgccggctctccccccaccccaccccgcccctcacatcatactccaatcataaccttgtatattacgcagtcattttggttttcgcggacgcgcctacctaagtaccatttacagaaagtgactctggctgtcattattttgtttatttgttccctatgcaaaaaaaaaatgaaaatgaaaaaagggggattccataaaagattcaataaaagacaaacaaaaaaaaaagaaaaaagaaaaaaatgtataaaaattaaacaagctatgcttcgactcttaaaaaaaaaaaaaaaaaa
//
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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