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2025-05-09 16:57:13, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001245002 8063 bp mRNA linear PRI 01-MAY-2013
DEFINITION Homo sapiens nuclear factor I/C (CCAAT-binding transcription
factor) (NFIC), transcript variant 1, mRNA.
ACCESSION NM_001245002
VERSION NM_001245002.1 GI:350529395
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 8063)
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 8063)
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 8063)
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 8063)
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 8063)
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 8063)
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 8063)
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 8063)
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 8063)
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 8063)
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,
AK297825.1, 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 (1) encodes the longest 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 :: AK297825.1 [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
1340-1735 AK297825.1 1322-1717
1736-2137 AK289885.1 1672-2073
2138-2497 CB053896.1 51-410 c
2498-3090 CK431049.1 45-637
3091-7781 AC005551.1 12615-17305
7782-8063 BU727954.1 1-282 c
FEATURES Location/Qualifiers
source 1..8063
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19p13.3"
gene 1..8063
/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..1597
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="isoform 1 is encoded by transcript variant 1;
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 1"
/protein_id="NP_001231931.1"
/db_xref="GI:350529396"
/db_xref="CCDS:CCDS59330.1"
/db_xref="GeneID:4782"
/db_xref="HGNC:7786"
/db_xref="MIM:600729"
/translation="
MYSSPLCLTQDEFHPFIEALLPHVRAFAYTWFNLQARKRKYFKKHEKRMSKDEERAVKDELLGEKPEVKQKWASRLLAKLRKDIRPECREDFVLSITGKKAPGCVLSNPDQKGKMRRIDCLRQADKVWRLDLVMVILFKGIPLESTDGERLVKAAQCGHPVLCVQPHHIGVAVKELDLYLAYFVRERDAEQSGSPRTGMGSDQEDSKPITLDTTDFQESFVTSGVFSVTELIQVSRTPVVTGTGPNFSLGELQGHLAYDLNPASTGLRRTLPSTSSSGSKRHKSGSMEEDVDTSPGGDYYTSPSSPTSSSRNWTEDMEGGISSPVKKTEMDKSPFNSPSPQDSPRLSSFTQHHRPVIAVHSGIARSPHPSSALHFPTTSILPQTASTYFPHTAIRYPPHLNPQDPLKDLVSLACDPASQQPGPLNGSGQLKMPSHCLSAQMLAPPPPGLPRLALPPATKPATTSEGGATSPTSPSYSPPDTSPANRSFVGLGPRDPAGIYQAQSWYLG
"
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..1594
/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"
misc_feature 1529..1531
/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..1493
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 1384
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:376400951"
variation 1404
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:199528650"
variation 1410
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:199905745"
variation 1436
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201510249"
variation 1447..1448
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:150025045"
variation 1460
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:76933523"
variation 1476
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:370906966"
variation 1480
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:373976044"
exon 1494..1579
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 1501
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:76459565"
variation 1503
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372572344"
variation 1526
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:376511703"
variation 1569
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:368331116"
exon 1580..8045
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
STS 1587..1712
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH70943"
/db_xref="UniSTS:18913"
variation 1604..1606
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="tct"
/db_xref="dbSNP:202152750"
variation 1646
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:374310905"
variation 1649
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370736060"
variation 1679
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:8047"
variation 1681
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:377580938"
variation 1738
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:62130570"
variation 1770
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:185384063"
variation 1821
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:369618261"
variation 1829
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:143763131"
variation 1907
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:147192339"
variation 1909..1910
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:35103414"
variation 1969
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:112297811"
variation 2021
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:371877071"
variation 2306
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:35033094"
variation 2362
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:189392307"
variation 2372
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:376897288"
variation 2595
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:115020939"
variation 2598
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:4807474"
variation 2732
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:116669109"
variation 2858
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373175985"
variation 2878
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:74656266"
variation 2903..2904
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:143359349"
variation 3003
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:10426917"
variation 3071
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:10426352"
variation 3118
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:140546305"
variation 3150
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:3746298"
variation 3151
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:3746299"
variation 3169
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:7258954"
variation 3326
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:115534300"
variation 3353
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:6510757"
variation 3529
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:191016688"
variation 3542
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:12971613"
variation 3623
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:142170418"
variation 3804
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:11673590"
STS 3818..3949
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH47688"
/db_xref="UniSTS:41852"
variation 3848
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:60093027"
variation 3948
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:713043"
variation 3952
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:11666623"
variation 3965
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:61089125"
variation 3980..3981
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:71782480"
variation 3991
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaaa"
/db_xref="dbSNP:71708589"
variation 4002..4003
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:59668846"
variation 4003..4007
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="gatac"
/db_xref="dbSNP:146468333"
variation 4003
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201570343"
variation 4005
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:369702439"
variation 4006
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:2392709"
variation 4007
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373239554"
variation 4010
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:377659423"
variation 4058
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:56294037"
variation 4152
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:11541514"
variation 4226..4230
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaat"
/db_xref="dbSNP:142281202"
variation 4230
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:370549069"
variation 4235
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaat"
/db_xref="dbSNP:71731809"
variation 4235
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:373766499"
variation 4242
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:377329843"
variation 4245
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370429651"
variation 4270
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:10617203"
variation 4283..4284
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="gg"
/db_xref="dbSNP:373260051"
variation 4510
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:150732039"
variation 4516
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:112962670"
variation 4527
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:190974806"
variation 4594
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:112077871"
variation 4612
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370523643"
variation 4657
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373678102"
variation 4708
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:371834921"
variation 4720
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:139103336"
variation 4901
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:116639605"
variation 5051..5052
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:11388112"
variation 5051
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201353930"
variation 5058..5059
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:200434679"
variation 5063
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:375507336"
variation 5222
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:182718334"
variation 5266
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:376532943"
variation 5300
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:149869150"
variation 5427
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:188692410"
variation 5438
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:191740254"
variation 5441
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:111606883"
variation 5486..5487
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:112243853"
variation 5522
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:73919194"
variation 5548
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:183256663"
variation 5581
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:368229276"
variation 5641
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:202195970"
variation 5688
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:373841623"
STS 5816..5976
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="A008X33"
/db_xref="UniSTS:11659"
variation 5864
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:148735510"
variation 5893
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:188079746"
variation 5923..5924
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:201187022"
variation 5929
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8112889"
variation 5930..5931
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:146782728"
variation 5930
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8108753"
variation 5931..5932
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:68098094"
variation 5933..5934
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:373716537"
variation 5936
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:148147968"
variation 5936
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8108755"
variation 5943..5944
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:59410286"
variation 5969
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:182356784"
variation 6041
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:374469121"
variation 6051
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="c"
/db_xref="dbSNP:11357750"
variation 6083
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:118139977"
variation 6134
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:187795070"
variation 6137
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:111969590"
variation 6288
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:192533268"
variation 6450
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:146433383"
variation 6537
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:73919195"
STS 6561..6697
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="G32369"
/db_xref="UniSTS:116958"
STS 6561..6697
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH67057"
/db_xref="UniSTS:84684"
variation 6586..6587
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatatat"
/db_xref="dbSNP:374523932"
variation 6586..6587
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:8110278"
variation 6586
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:28665162"
variation 6587..6606
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatat"
/db_xref="dbSNP:375414685"
variation 6587..6588
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatatat"
/replace="atatattatatatatatatat"
/db_xref="dbSNP:34605422"
variation 6594
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:185019123"
variation 6609
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:190207945"
variation 6619..6620
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:35325992"
variation 6652
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:8113786"
variation 6690
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:192998513"
variation 6722
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:116148466"
variation 6762
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:72974787"
variation 6795
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:140704632"
variation 6820
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:8110928"
variation 6836
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372237245"
variation 7018..7019
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:377115512"
variation 7023
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:374793831"
variation 7026
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:369655483"
variation 7154
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:184806177"
variation 7281
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:74741143"
variation 7333
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:4807475"
variation 7414
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:188683808"
variation 7443
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:376460082"
variation 7483
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:144557238"
variation 7542..7543
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:199586457"
variation 7593..7595
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="ctt"
/db_xref="dbSNP:370673109"
variation 7595..7597
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="tct"
/db_xref="dbSNP:57761031"
variation 7605
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:180737599"
variation 7668
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:185090028"
variation 7768
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:369940873"
variation 7792
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:146638802"
STS 7795..7922
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="WI-12079"
/db_xref="UniSTS:15156"
variation 7799
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:35160631"
STS 7810..7926
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH36034"
/db_xref="UniSTS:47850"
variation 7813
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:189164209"
variation 7832
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:10417031"
variation 7885
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:141326218"
variation 7908
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:11547206"
variation 7980..7983
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="acaa"
/db_xref="dbSNP:199877074"
variation 7982..7986
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaca"
/db_xref="dbSNP:147791651"
variation 7982
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaca"
/db_xref="dbSNP:71715433"
variation 7985..7989
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:146550572"
variation 7985
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:10543929"
variation 7985
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:60861688"
variation 7989
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:373990617"
variation 7990..7991
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="ag"
/db_xref="dbSNP:71656643"
variation 7991
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:12983451"
polyA_signal 8020..8025
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
polyA_site 8045
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
ORIGIN
tttggaaaaatgactcagtaagttcagcgcgcccgctccggccggccctgcgcctcccgccgcgcccgggatgtattcgtccccgctctgcctcacccaggatgagttccacccgttcatcgaggccctgctgcctcacgtccgcgccttcgcctacacctggttcaacctgcaggcgcggaagcgcaagtacttcaagaagcacgagaagcggatgtcgaaggacgaggagcgtgcggtcaaggacgagctgctgggcgagaagcccgaggtcaagcagaagtgggcgtcgcggctgctggccaagctgcgcaaggacatccggcccgagtgccgcgaggacttcgtgctgagcatcaccggcaagaaggcgccgggctgcgtgctctccaaccccgaccagaagggcaagatgcggcgcatcgactgtctccggcaggcggacaaggtgtggcggctggacctggtcatggtcatcctgttcaagggcatcccgctggagagcaccgacggcgagcgcctggtcaaggctgcgcagtgcggtcacccggtcctgtgcgtgcagccgcaccacattggcgtggccgtcaaggagctggacctctacctggcctacttcgtgcgtgagcgagatgcagagcaaagcggcagtccccggacagggatgggctctgaccaggaggacagcaagcccatcacgctggacacgaccgacttccaggagagctttgtcacctccggcgtgttcagcgtcactgagctcatccaagtgtcccggacacccgtggtgactggaacaggacccaacttctccctgggggagctgcaggggcacctggcatacgacctgaacccagccagcactggcctcagaagaacgctgcccagcacctcctccagtgggagcaagcggcacaaatcgggctcgatggaggaagacgtggacacgagccctggcggcgattactacacttcgcccagctcgcccacgagtagcagccgcaactggacggaggacatggaaggaggcatctcgtccccggtgaagaagacagagatggacaagtcaccattcaacagcccgtccccccaggactctccccgcctctccagcttcacccagcaccaccggcccgtcatcgccgtgcacagcgggatcgcccggagcccacacccgtcctccgctctgcatttccctacgacgtccatcctaccccagacggcctccacctacttcccccacacggccatccgctacccacctcatctcaacccccaggacccgctcaaagatcttgtctcgctggcctgcgacccagccagccagcaacctggaccgttaaatggaagtggtcagctcaaaatgcccagccactgcctttctgctcagatgctggcacctccgcccccggggctgccacggctggcgctcccccctgccaccaaacccgccaccacctccgagggaggagccacgtcgccgacctcgccttcctactctccgcccgacacgtcccctgcaaaccgttcctttgtgggattaggaccaagggatcctgcgggcatttatcaggcacagtcctggtatctgggatagcaaaggtcttcttccctcgccccttctccatcgtcccaggaatcccagggggcagcacagccggcccccggcccacgttttcggtggaaaattagagtgaacaagaacacccctgccgactcccagcccggccaaaaagacaaaacacatagacgcacacactcaggaggaaaagaaaaaacaaaggcagaagaagaagaagaagaaataaaaacccacccaagcaagaagacaaaaggtaaagacgcaacgtttccaactctcgggacgccaaggccgcaggactggagggccaggccccgccacccccacgggagacccgggacagggcgtcttcctaagttattcatctcctctccgcctgctgctcgggaaggacagacgccggccgcccgcccgcgccccggaggccctggctctgtccggagaccaggtgagcacagcctggagcctgtgcccagggccgacaggcgcgacacccagcaaggccacctctccccgggcccccgcgcctctgccggacacggaccggcccctcagcccccaccgaggacgcagccactggggggaaagggagacacagcggaccccggccgggcagcggagaccgcagaggcgggcagggtggggcaggcgagtggtgtcgcgggggtgcgtggcgcttgcgagccctggccaggggaggaagtgaggcccaggcacctgctgcccctcgagggggccctgcctgccgcggggcctccccacaagcccctcccaaagcgccggccgactcgctgtctcgctggggactctttcagccctcgcgcccgcccgtttgggaggagaagtctctatgcaattggccccggcccctccaccccccacccccggcataggaggcccccccacctcgcccggctcacacccccaaagggagggacccacattgcacacactgtaagaaatgcactttccgaggaaggggatgggggagcccggacacccagagctccccgagttgggggtgcccgtctggagcgcccccgtcagcccctggcggtgggaggtgagagcgagtggtttaagtgcctgattaccaccacccgcccccccctttgtccagctgggacacggaatggccgcgggcctcctccccctcccctccagcctctccaccagcccctccagtcaaccctcatcgccgtgcccccccagagctagagagatggggcccctgcgtggcccgaggggcagagctgggcgtcacttcgcaagcgtcctgccctgccggggcgcgggggtgggctctggggaagccggtgcgccccccacgcctccgctgccagtgccttacattctggagcgacccccctccctggtgcctcccagcgaagggggaccgccgtttgcactttcatcgcctaccccgacgcggggcccagctgcgggacgtgcatcacggctgggcccccagaggagagaggaggccgacgccagcggtccccgctcggaacggggagggttttcggggggttcggcgtcgcaccttggggccccccgcagccgtgtagggggcctcccatctgctaagcgtttttccgttgagccgctccaaaaacactaagctggggacgccaggtgcccccccaccccggctccctggccctatccacacctccacccccaccccaggatcgccatctttaggggaggcctgggagggggtgttaggtgttttagggccaccgagctcaaacacaaggacccctccccggcccacccagcccagccccaactgacctccatgcctagggaaaaactccccccaccactgccccctcccccgacccaggccaaagccagggcaggtctccgggtctcacctgctcctagcctcacccccctgcccccgaaaaccagactctcctcccaaactagcctcaggagcttggcgaacccgctcgctcctaaagagaaagacccaggaccctcccccatcacccccaagagaggttcgccatcctctggcctcgagcccttggtccctccgtccgtctgtcctcggggcccgctcccccggtggcccttggggatcaaagcgtgggccgctctccgggagggcgggcgggggagggggtggtcgggttgtgccattggggtgtccggaagcttctcagccagggtgggggtcgtggagtgggggagggaggccagccgggctccagaggggtcagggcgcgacgagaaccaactctttacctaactttgcatggtgcttagtcaaggactcctgcgacctggctcccgaggtcagctggcggcgctgacacacatgcatggcagactatccctggctctatctccctgttcctcgccccctccaccccccacttcctctttaaaaaaaaaaaaaaaaaaaaaaagatacaagaaaaacctttaaaaaaattccatgtttcctaatttgcacgaaattttctaccacaagatgtgccttgccttccgagaataagtattacctttaaacaatatcagcgcacacacatagctgcatgttctgctcgtgtagtttaaaaaaaaaaagacaaaacagtgacatgaaataaaaaataaaaattgaaaagggatgtatttctatttgtaaaaaaaataaaataaaaaataagaaagtgagaatctaaaaaaaaaaaaaaaaaaaaaaaaggaagaaaaaccacgctaaaaatcaagccactgaaaacaattgcccccaggtctacccagcccctggctgtccttggtcctgtctcccctcctgctgtattcaggggtgccccctggtgctcagcctctaccacccccaaccctgctcttgggtacccagaggggtcatttctgaatcccttgcccagaggacagacctccggggcccatcttggccctgggaaagggctctcctctctgattggtccctaggccacgggccggcccccagacaccattcaccgacccactgcaggctgtcctccaaccatggggtggccactccacccgcagccagactccccgctccccacttttcatgcaggctggcatacccctggctcagggtcaaatgctgttccacacccacctcagaggcaccccctctcccctgccccgtgcatccccacccttcttgccaaaggacctcttttcccctatccagagaccaccccaggtggcattctctcccaccttctcctttgtcccccatcccctgtctctgtcttccagctgtgaatatgaagggtatcctgtatgaaacaaaaacaaaacctgatatatgcaatatctgtctgtctgtctgtacccatgggcctggctcagccattggaggcccagccgagggtccggcagggcacagggacagccaggtggcaccgagtcacaggctgtggtccggtggctgagcatgctgttgtcttgtccttgattttattttcttttgttctttttttttttcttttctttttgtttttaactccagcttcctttgctttttacttgaccaaagctaagacaatagccagatggttagtggggcagccaggcagggaggacccagggctgggattctccaaccttaggccattcctgcagccctcaccacctccagcccctccaagcatctcgtgtagggacccacgcagatggtcccattcattcactattgcccccaaccccgggattttgggtggtctccacagccaccatcatacactcatcccgtgttttcttccaaaaagtcacctcagcagcctccccaggcgatacagagggagagcccagaccaccacagctggccacgacattgcccttaagtaatatgcattggccagagagcccgggctggctgtgcacagcattcatgtagctgatttctagctttttttttttttctgccccactcctgagcaaatctgtcttgccaaggaactaggagcaaccggaggcaaagggagtgggtggccccatcactattgggaccatcgcgtccctgcacagcccacacccgggggcccagagtcctgggctggacgccacccttctcaccccgagcttgcctccttggctcacttggcaccttggctgagtacagcaggcaaaagcccataccaggcagcatgttgtggatggtttagttctccccgcctccctgtttcttggaaaagctacagggtccctgtagggcaaaattcccaggcgccttgctgcagacagagtaagacaaaaacaccaggaagcaggattccgtgcccatctctgcagtttgggttcacaaaagggggtgccgtcatccctgggtggaggagggagtgttggttttttgtttttgtttttttaacatgtatgaaactgacatcttctcaaatcttgttccacccccctctggaagcccccatcacccacccctgctatggacaccacacctatgccaggcccccccccccaccccagtctcattctggggtctgcccatgctgtgggaaagaatagggaggcctcccaaatatatgcaaattgtccccattccgtgggggcacctgacaatgacccgggtggagatggggcatggaggagtaggaagacccagccctatttgactggggagaggaggatctggagtccttcatgcccaggtctggaacccaggttctgaccccagggccccaccctgggctggacaatcagatcccaaaggaatgccaaaggggactcggttgggagagccgcttaggggccagacctgggtccccctgcaggtccccaggcagcagacaattccaccttccctgccccaggaccttgagagacagcagcattccaggcacagacagacttggctgcaccccactgtcccttgcaagacaggttctggagccaggagcaactgtccagccctccagaagagacagcaagcagcccccctacccactctggcctccccaatggtactttgacctccagtgtagggctatactatacatatatatatatatatatatatatatatataattttggaatttgtttctcataatacagaatatatagtggctaccttgtatcttggtctggattctctctctgagaccccggattttactttctctttggagggcgctgggacatacatctctcaatccagcttcctccgcatcctcccatcttgccccatttctgccacgtcagacacttcctgagagtctcaccttcaaaatgacaccgctgcccatccattgctcaatggtacagagtgtggggtcagtccaccacccttgacctcccggcagggcaaggtgaggaggcggacccaaagcagtaccagcaggacttgttgccagtgataccaaaacagacttttcccaagcagtgcctcacatgtctgctggtgtggctttgggattctcctgccccacccccccgtccatggcagccccctccccaaggctttgctcacacctgagacaggaaggaggaaggggatccaataggaatatgggccccggaggggaagtcatgcacccccaagccaccaccccccagccttccacgcacatctcctggctggaagagagccctccaaaaaggggacacaggctgccccggcccctcaactgcatccacaccccatcctctcatcttgggtcccagccaggcccccccaaaaccaaagccccctcaagtcctggggtcccagcctgtgcccccagcttcctgcccacccagccctgagcattctcacacagagaaagaacaagcaagggctccagggggacaggatggggcagggcatacagtggggggtgggggggcagctgggaggagggagggacaaaacaaaacattttcctttgggttttttttttctttcttttttctcccctttactctttgggtggtgttgcttttcctttccttttccctttgagatttttttgttgttgtttcctttttgtattttactgatatcaccaggatagtttactctccttctagctttctgcttaccgcacactggataacacacacatacacacccacaaaaatgctcatgaacccaatccggagaaggttccagcaggtcccccaccctcccctcctcctcctacttctcctcttgacagcgaggacaggagggggacaaggggacacctgggcagacccgccggctctccccccaccccaccccgcccctcacatcatactccaatcataaccttgtatattacgcagtcattttggttttcgcggacgcgcctacctaagtaccatttacagaaagtgactctggctgtcattattttgtttatttgttccctatgcaaaaaaaaaatgaaaatgaaaaaagggggattccataaaagattcaataaaagacaaacaaaaaaaaaagaaaaaagaaaaaaatgtataaaaattaaacaagctatgcttcgactcttaaaaaaaaaaaaaaaaaa
//
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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