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2025-05-09 17:17:29, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_205843 8086 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens nuclear factor I/C (CCAAT-binding transcription
factor) (NFIC), transcript variant 2, mRNA.
ACCESSION NM_205843
VERSION NM_205843.2 GI:350529394
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 8086)
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 8086)
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 8086)
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 8086)
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 8086)
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 8086)
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 8086)
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 8086)
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 8086)
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 8086)
AUTHORS Santoro,C., Mermod,N., Andrews,P.C. and Tjian,R.
TITLE A family of human CCAAT-box-binding proteins active in
transcription and DNA replication: cloning and expression of
multiple cDNAs
JOURNAL Nature 334 (6179), 218-224 (1988)
PUBMED 3398920
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BP279194.1, AK289885.1,
CB053896.1, CK431049.1, AC005551.1 and BU727954.1.
This sequence is a reference standard in the RefSeqGene project.
On Oct 8, 2011 this sequence version replaced gi:45505150.
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 (2) contains an alternate 5'
terminal exon compared to variant 1. This results in translation
initiation from an alternate start codon, and a shorter isoform (2)
with a distinct N-terminus compared to isoform 1.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AK289885.1, X12492.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025084, ERS025085 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-87 BP279194.1 1-87
88-2160 AK289885.1 1-2073
2161-2520 CB053896.1 51-410 c
2521-3113 CK431049.1 45-637
3114-7804 AC005551.1 12615-17305
7805-8086 BU727954.1 1-282 c
FEATURES Location/Qualifiers
source 1..8086
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="19"
/map="19p13.3"
gene 1..8086
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="nuclear factor I/C (CCAAT-binding transcription
factor)"
/db_xref="GeneID:4782"
/db_xref="HGNC:7786"
/db_xref="MIM:600729"
exon 1..123
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
CDS 121..1620
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="isoform 2 is encoded by transcript variant 2;
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 2"
/protein_id="NP_995315.1"
/db_xref="GI:45505151"
/db_xref="CCDS:CCDS45914.1"
/db_xref="GeneID:4782"
/db_xref="HGNC:7786"
/db_xref="MIM:600729"
/translation="
MDEFHPFIEALLPHVRAFAYTWFNLQARKRKYFKKHEKRMSKDEERAVKDELLGEKPEVKQKWASRLLAKLRKDIRPECREDFVLSITGKKAPGCVLSNPDQKGKMRRIDCLRQADKVWRLDLVMVILFKGIPLESTDGERLVKAAQCGHPVLCVQPHHIGVAVKELDLYLAYFVRERDAEQSGSPRTGMGSDQEDSKPITLDTTDFQESFVTSGVFSVTELIQVSRTPVVTGTGPNFSLGELQGHLAYDLNPASTGLRRTLPSTSSSGSKRHKSGSMEEDVDTSPGGDYYTSPSSPTSSSRNWTEDMEGGISSPVKKTEMDKSPFNSPSPQDSPRLSSFTQHHRPVIAVHSGIARSPHPSSALHFPTTSILPQTASTYFPHTAIRYPPHLNPQDPLKDLVSLACDPASQQPGPLNGSGQLKMPSHCLSAQMLAPPPPGLPRLALPPATKPATTSEGGATSPTSPSYSPPDTSPANRSFVGLGPRDPAGIYQAQSWYLG
"
misc_feature 124..234
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="Nuclear factor I protein pre-N-terminus; Region:
NfI_DNAbd_pre-N; pfam10524"
/db_xref="CDD:151076"
misc_feature 295..600
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/note="N-terminal Mad Homology 1 (MH1) domain; Region:
MH1; cl00055"
/db_xref="CDD:206806"
misc_feature 667..669
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 673..675
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 742..1617
/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 1060..1062
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1090..1092
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1102..1104
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1108..1110
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1108..1110
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
exon 124..655
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 154
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:190753458"
variation 174
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:144268546"
variation 201
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:148748813"
variation 203
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:141482719"
variation 213
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370694661"
variation 219
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:150819987"
variation 238
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:139273924"
variation 261
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:201762449"
variation 321
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:144458967"
variation 385
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:146638960"
variation 396
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:367554475"
variation 399
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:369119535"
variation 407
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:61731129"
variation 465
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:199785054"
variation 519
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:146650773"
variation 534
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372862380"
variation 561
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:375768351"
variation 571
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:201434711"
variation 583
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:200551240"
variation 585
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:11878387"
variation 590
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:138699938"
variation 636
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201632995"
variation 642
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372436353"
variation 643
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:201510675"
variation 646
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:369796013"
variation 653
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:201011953"
exon 656..727
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 659
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:145828739"
variation 663
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:369261498"
variation 670
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:200153960"
variation 688
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:78728474"
variation 723
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:371331059"
exon 728..802
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 732
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:377664780"
variation 762
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:111422145"
variation 763
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:143519997"
variation 774
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201124721"
variation 777
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:138225094"
variation 800
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:116865554"
exon 803..926
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 807
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:150930822"
variation 831
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:374471241"
variation 837
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:112569402"
variation 864
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:373306178"
variation 887
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:35952068"
variation 902..903
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:34108601"
variation 908
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:368371894"
exon 927..1051
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 942
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:146070921"
variation 945
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:138945457"
variation 946
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:142790393"
variation 951
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:369569353"
variation 972..973
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/db_xref="dbSNP:34937859"
variation 983
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:373904141"
variation 1016
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:200221249"
variation 1035
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:377153122"
variation 1041
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:369185182"
exon 1052..1177
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 1122
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:117114356"
variation 1127
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:200686979"
variation 1155
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:199780384"
variation 1164
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:149374084"
variation 1167
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:375318776"
exon 1178..1362
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 1206
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:138179732"
variation 1244
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:374896582"
variation 1245
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:142781909"
variation 1248
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:201575539"
variation 1257
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:146145775"
variation 1260
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:372361568"
variation 1269
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:200793537"
variation 1277
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:140170107"
variation 1302
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:11671446"
variation 1305
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:142476049"
variation 1308
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:368456734"
variation 1317
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:141932371"
variation 1335
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:1060363"
variation 1342
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:10412720"
variation 1362
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:372367068"
exon 1363..1516
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 1407
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:376400951"
variation 1427
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:199528650"
variation 1433
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:199905745"
variation 1459
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201510249"
variation 1470..1471
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:150025045"
variation 1483
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:76933523"
variation 1499
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:370906966"
variation 1503
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:373976044"
exon 1517..1602
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
variation 1524
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:76459565"
variation 1526
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372572344"
variation 1549
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:376511703"
variation 1592
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:368331116"
exon 1603..8068
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/inference="alignment:Splign:1.39.8"
STS 1610..1735
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH70943"
/db_xref="UniSTS:18913"
variation 1627..1629
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="tct"
/db_xref="dbSNP:202152750"
variation 1669
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:374310905"
variation 1672
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370736060"
variation 1702
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:8047"
variation 1704
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:377580938"
variation 1761
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:62130570"
variation 1793
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:185384063"
variation 1844
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:369618261"
variation 1852
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:143763131"
variation 1930
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:147192339"
variation 1932..1933
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:35103414"
variation 1992
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:112297811"
variation 2044
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:371877071"
variation 2329
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:35033094"
variation 2385
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:189392307"
variation 2395
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:376897288"
variation 2618
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:115020939"
variation 2621
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:4807474"
variation 2755
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:116669109"
variation 2881
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373175985"
variation 2901
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:74656266"
variation 2926..2927
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:143359349"
variation 3026
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:10426917"
variation 3094
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:10426352"
variation 3141
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:140546305"
variation 3173
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:3746298"
variation 3174
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:3746299"
variation 3192
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:7258954"
variation 3349
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:115534300"
variation 3376
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:6510757"
variation 3552
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:191016688"
variation 3565
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:12971613"
variation 3646
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:142170418"
variation 3827
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:11673590"
STS 3841..3972
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH47688"
/db_xref="UniSTS:41852"
variation 3871
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:60093027"
variation 3971
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:713043"
variation 3975
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:11666623"
variation 3988
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:61089125"
variation 4003..4004
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:71782480"
variation 4014
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaaa"
/db_xref="dbSNP:71708589"
variation 4025..4026
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:59668846"
variation 4026..4030
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="gatac"
/db_xref="dbSNP:146468333"
variation 4026
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201570343"
variation 4028
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:369702439"
variation 4029
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:2392709"
variation 4030
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373239554"
variation 4033
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:377659423"
variation 4081
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:56294037"
variation 4175
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:11541514"
variation 4249..4253
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaat"
/db_xref="dbSNP:142281202"
variation 4253
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:370549069"
variation 4258
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaat"
/db_xref="dbSNP:71731809"
variation 4258
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:373766499"
variation 4265
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:377329843"
variation 4268
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370429651"
variation 4293
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:10617203"
variation 4306..4307
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="gg"
/db_xref="dbSNP:373260051"
variation 4533
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:150732039"
variation 4539
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:112962670"
variation 4550
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:190974806"
variation 4617
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:112077871"
variation 4635
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:370523643"
variation 4680
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:373678102"
variation 4731
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:371834921"
variation 4743
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:139103336"
variation 4924
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:116639605"
variation 5074..5075
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:11388112"
variation 5074
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:201353930"
variation 5081..5082
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:200434679"
variation 5086
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:375507336"
variation 5245
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:182718334"
variation 5289
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:376532943"
variation 5323
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:149869150"
variation 5450
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:188692410"
variation 5461
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:191740254"
variation 5464
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:111606883"
variation 5509..5510
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:112243853"
variation 5545
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="t"
/db_xref="dbSNP:73919194"
variation 5571
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:183256663"
variation 5604
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:368229276"
variation 5664
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:202195970"
variation 5711
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:373841623"
STS 5839..5999
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="A008X33"
/db_xref="UniSTS:11659"
variation 5887
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:148735510"
variation 5916
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:188079746"
variation 5946..5947
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:201187022"
variation 5952
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8112889"
variation 5953..5954
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:146782728"
variation 5953
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8108753"
variation 5954..5955
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:68098094"
variation 5956..5957
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:373716537"
variation 5959
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:148147968"
variation 5959
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:8108755"
variation 5966..5967
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:59410286"
variation 5992
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/db_xref="dbSNP:182356784"
variation 6064
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:374469121"
variation 6074
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="a"
/replace="c"
/db_xref="dbSNP:11357750"
variation 6106
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:118139977"
variation 6157
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:187795070"
variation 6160
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:111969590"
variation 6311
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:192533268"
variation 6473
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:146433383"
variation 6560
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:73919195"
STS 6584..6720
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="G32369"
/db_xref="UniSTS:116958"
STS 6584..6720
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH67057"
/db_xref="UniSTS:84684"
variation 6609..6610
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatatat"
/db_xref="dbSNP:374523932"
variation 6609..6610
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:8110278"
variation 6609
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:28665162"
variation 6610..6629
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatat"
/db_xref="dbSNP:375414685"
variation 6610..6611
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="atatatatatatatatatatat"
/replace="atatattatatatatatatat"
/db_xref="dbSNP:34605422"
variation 6617
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:185019123"
variation 6632
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:190207945"
variation 6642..6643
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="t"
/db_xref="dbSNP:35325992"
variation 6675
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:8113786"
variation 6713
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:192998513"
variation 6745
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:116148466"
variation 6785
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:72974787"
variation 6818
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:140704632"
variation 6843
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:8110928"
variation 6859
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:372237245"
variation 7041..7042
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="c"
/db_xref="dbSNP:377115512"
variation 7046
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:374793831"
variation 7049
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:369655483"
variation 7177
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:184806177"
variation 7304
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:74741143"
variation 7356
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:4807475"
variation 7437
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:188683808"
variation 7466
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:376460082"
variation 7506
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:144557238"
variation 7565..7566
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="g"
/db_xref="dbSNP:199586457"
variation 7616..7618
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="ctt"
/db_xref="dbSNP:370673109"
variation 7618..7620
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="tct"
/db_xref="dbSNP:57761031"
variation 7628
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:180737599"
variation 7691
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:185090028"
variation 7791
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:369940873"
variation 7815
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:146638802"
STS 7818..7945
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="WI-12079"
/db_xref="UniSTS:15156"
variation 7822
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="t"
/db_xref="dbSNP:35160631"
STS 7833..7949
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/standard_name="RH36034"
/db_xref="UniSTS:47850"
variation 7836
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:189164209"
variation 7855
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:10417031"
variation 7908
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:141326218"
variation 7931
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="g"
/replace="t"
/db_xref="dbSNP:11547206"
variation 8003..8006
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="acaa"
/db_xref="dbSNP:199877074"
variation 8005..8009
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaca"
/db_xref="dbSNP:147791651"
variation 8005
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="aaaca"
/db_xref="dbSNP:71715433"
variation 8008..8012
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:146550572"
variation 8008
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="c"
/db_xref="dbSNP:10543929"
variation 8008
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:60861688"
variation 8012
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="caaaa"
/db_xref="dbSNP:373990617"
variation 8013..8014
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace=""
/replace="ag"
/db_xref="dbSNP:71656643"
variation 8014
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
/replace="a"
/replace="g"
/db_xref="dbSNP:12983451"
polyA_signal 8043..8048
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
polyA_site 8068
/gene="NFIC"
/gene_synonym="CTF; CTF5; NF-I; NFI"
ORIGIN
gctcgctccctcccccgcgcgccctccctcgccgcctcctcccgccgcctgcggcccccccctcgccggggaccgagcgcgctcgctccggcgccggcctcgcctcctcgcagcagcgccatggatgagttccacccgttcatcgaggccctgctgcctcacgtccgcgccttcgcctacacctggttcaacctgcaggcgcggaagcgcaagtacttcaagaagcacgagaagcggatgtcgaaggacgaggagcgtgcggtcaaggacgagctgctgggcgagaagcccgaggtcaagcagaagtgggcgtcgcggctgctggccaagctgcgcaaggacatccggcccgagtgccgcgaggacttcgtgctgagcatcaccggcaagaaggcgccgggctgcgtgctctccaaccccgaccagaagggcaagatgcggcgcatcgactgtctccggcaggcggacaaggtgtggcggctggacctggtcatggtcatcctgttcaagggcatcccgctggagagcaccgacggcgagcgcctggtcaaggctgcgcagtgcggtcacccggtcctgtgcgtgcagccgcaccacattggcgtggccgtcaaggagctggacctctacctggcctacttcgtgcgtgagcgagatgcagagcaaagcggcagtccccggacagggatgggctctgaccaggaggacagcaagcccatcacgctggacacgaccgacttccaggagagctttgtcacctccggcgtgttcagcgtcactgagctcatccaagtgtcccggacacccgtggtgactggaacaggacccaacttctccctgggggagctgcaggggcacctggcatacgacctgaacccagccagcactggcctcagaagaacgctgcccagcacctcctccagtgggagcaagcggcacaaatcgggctcgatggaggaagacgtggacacgagccctggcggcgattactacacttcgcccagctcgcccacgagtagcagccgcaactggacggaggacatggaaggaggcatctcgtccccggtgaagaagacagagatggacaagtcaccattcaacagcccgtccccccaggactctccccgcctctccagcttcacccagcaccaccggcccgtcatcgccgtgcacagcgggatcgcccggagcccacacccgtcctccgctctgcatttccctacgacgtccatcctaccccagacggcctccacctacttcccccacacggccatccgctacccacctcatctcaacccccaggacccgctcaaagatcttgtctcgctggcctgcgacccagccagccagcaacctggaccgttaaatggaagtggtcagctcaaaatgcccagccactgcctttctgctcagatgctggcacctccgcccccggggctgccacggctggcgctcccccctgccaccaaacccgccaccacctccgagggaggagccacgtcgccgacctcgccttcctactctccgcccgacacgtcccctgcaaaccgttcctttgtgggattaggaccaagggatcctgcgggcatttatcaggcacagtcctggtatctgggatagcaaaggtcttcttccctcgccccttctccatcgtcccaggaatcccagggggcagcacagccggcccccggcccacgttttcggtggaaaattagagtgaacaagaacacccctgccgactcccagcccggccaaaaagacaaaacacatagacgcacacactcaggaggaaaagaaaaaacaaaggcagaagaagaagaagaagaaataaaaacccacccaagcaagaagacaaaaggtaaagacgcaacgtttccaactctcgggacgccaaggccgcaggactggagggccaggccccgccacccccacgggagacccgggacagggcgtcttcctaagttattcatctcctctccgcctgctgctcgggaaggacagacgccggccgcccgcccgcgccccggaggccctggctctgtccggagaccaggtgagcacagcctggagcctgtgcccagggccgacaggcgcgacacccagcaaggccacctctccccgggcccccgcgcctctgccggacacggaccggcccctcagcccccaccgaggacgcagccactggggggaaagggagacacagcggaccccggccgggcagcggagaccgcagaggcgggcagggtggggcaggcgagtggtgtcgcgggggtgcgtggcgcttgcgagccctggccaggggaggaagtgaggcccaggcacctgctgcccctcgagggggccctgcctgccgcggggcctccccacaagcccctcccaaagcgccggccgactcgctgtctcgctggggactctttcagccctcgcgcccgcccgtttgggaggagaagtctctatgcaattggccccggcccctccaccccccacccccggcataggaggcccccccacctcgcccggctcacacccccaaagggagggacccacattgcacacactgtaagaaatgcactttccgaggaaggggatgggggagcccggacacccagagctccccgagttgggggtgcccgtctggagcgcccccgtcagcccctggcggtgggaggtgagagcgagtggtttaagtgcctgattaccaccacccgcccccccctttgtccagctgggacacggaatggccgcgggcctcctccccctcccctccagcctctccaccagcccctccagtcaaccctcatcgccgtgcccccccagagctagagagatggggcccctgcgtggcccgaggggcagagctgggcgtcacttcgcaagcgtcctgccctgccggggcgcgggggtgggctctggggaagccggtgcgccccccacgcctccgctgccagtgccttacattctggagcgacccccctccctggtgcctcccagcgaagggggaccgccgtttgcactttcatcgcctaccccgacgcggggcccagctgcgggacgtgcatcacggctgggcccccagaggagagaggaggccgacgccagcggtccccgctcggaacggggagggttttcggggggttcggcgtcgcaccttggggccccccgcagccgtgtagggggcctcccatctgctaagcgtttttccgttgagccgctccaaaaacactaagctggggacgccaggtgcccccccaccccggctccctggccctatccacacctccacccccaccccaggatcgccatctttaggggaggcctgggagggggtgttaggtgttttagggccaccgagctcaaacacaaggacccctccccggcccacccagcccagccccaactgacctccatgcctagggaaaaactccccccaccactgccccctcccccgacccaggccaaagccagggcaggtctccgggtctcacctgctcctagcctcacccccctgcccccgaaaaccagactctcctcccaaactagcctcaggagcttggcgaacccgctcgctcctaaagagaaagacccaggaccctcccccatcacccccaagagaggttcgccatcctctggcctcgagcccttggtccctccgtccgtctgtcctcggggcccgctcccccggtggcccttggggatcaaagcgtgggccgctctccgggagggcgggcgggggagggggtggtcgggttgtgccattggggtgtccggaagcttctcagccagggtgggggtcgtggagtgggggagggaggccagccgggctccagaggggtcagggcgcgacgagaaccaactctttacctaactttgcatggtgcttagtcaaggactcctgcgacctggctcccgaggtcagctggcggcgctgacacacatgcatggcagactatccctggctctatctccctgttcctcgccccctccaccccccacttcctctttaaaaaaaaaaaaaaaaaaaaaaagatacaagaaaaacctttaaaaaaattccatgtttcctaatttgcacgaaattttctaccacaagatgtgccttgccttccgagaataagtattacctttaaacaatatcagcgcacacacatagctgcatgttctgctcgtgtagtttaaaaaaaaaaagacaaaacagtgacatgaaataaaaaataaaaattgaaaagggatgtatttctatttgtaaaaaaaataaaataaaaaataagaaagtgagaatctaaaaaaaaaaaaaaaaaaaaaaaaggaagaaaaaccacgctaaaaatcaagccactgaaaacaattgcccccaggtctacccagcccctggctgtccttggtcctgtctcccctcctgctgtattcaggggtgccccctggtgctcagcctctaccacccccaaccctgctcttgggtacccagaggggtcatttctgaatcccttgcccagaggacagacctccggggcccatcttggccctgggaaagggctctcctctctgattggtccctaggccacgggccggcccccagacaccattcaccgacccactgcaggctgtcctccaaccatggggtggccactccacccgcagccagactccccgctccccacttttcatgcaggctggcatacccctggctcagggtcaaatgctgttccacacccacctcagaggcaccccctctcccctgccccgtgcatccccacccttcttgccaaaggacctcttttcccctatccagagaccaccccaggtggcattctctcccaccttctcctttgtcccccatcccctgtctctgtcttccagctgtgaatatgaagggtatcctgtatgaaacaaaaacaaaacctgatatatgcaatatctgtctgtctgtctgtacccatgggcctggctcagccattggaggcccagccgagggtccggcagggcacagggacagccaggtggcaccgagtcacaggctgtggtccggtggctgagcatgctgttgtcttgtccttgattttattttcttttgttctttttttttttcttttctttttgtttttaactccagcttcctttgctttttacttgaccaaagctaagacaatagccagatggttagtggggcagccaggcagggaggacccagggctgggattctccaaccttaggccattcctgcagccctcaccacctccagcccctccaagcatctcgtgtagggacccacgcagatggtcccattcattcactattgcccccaaccccgggattttgggtggtctccacagccaccatcatacactcatcccgtgttttcttccaaaaagtcacctcagcagcctccccaggcgatacagagggagagcccagaccaccacagctggccacgacattgcccttaagtaatatgcattggccagagagcccgggctggctgtgcacagcattcatgtagctgatttctagctttttttttttttctgccccactcctgagcaaatctgtcttgccaaggaactaggagcaaccggaggcaaagggagtgggtggccccatcactattgggaccatcgcgtccctgcacagcccacacccgggggcccagagtcctgggctggacgccacccttctcaccccgagcttgcctccttggctcacttggcaccttggctgagtacagcaggcaaaagcccataccaggcagcatgttgtggatggtttagttctccccgcctccctgtttcttggaaaagctacagggtccctgtagggcaaaattcccaggcgccttgctgcagacagagtaagacaaaaacaccaggaagcaggattccgtgcccatctctgcagtttgggttcacaaaagggggtgccgtcatccctgggtggaggagggagtgttggttttttgtttttgtttttttaacatgtatgaaactgacatcttctcaaatcttgttccacccccctctggaagcccccatcacccacccctgctatggacaccacacctatgccaggcccccccccccaccccagtctcattctggggtctgcccatgctgtgggaaagaatagggaggcctcccaaatatatgcaaattgtccccattccgtgggggcacctgacaatgacccgggtggagatggggcatggaggagtaggaagacccagccctatttgactggggagaggaggatctggagtccttcatgcccaggtctggaacccaggttctgaccccagggccccaccctgggctggacaatcagatcccaaaggaatgccaaaggggactcggttgggagagccgcttaggggccagacctgggtccccctgcaggtccccaggcagcagacaattccaccttccctgccccaggaccttgagagacagcagcattccaggcacagacagacttggctgcaccccactgtcccttgcaagacaggttctggagccaggagcaactgtccagccctccagaagagacagcaagcagcccccctacccactctggcctccccaatggtactttgacctccagtgtagggctatactatacatatatatatatatatatatatatatatataattttggaatttgtttctcataatacagaatatatagtggctaccttgtatcttggtctggattctctctctgagaccccggattttactttctctttggagggcgctgggacatacatctctcaatccagcttcctccgcatcctcccatcttgccccatttctgccacgtcagacacttcctgagagtctcaccttcaaaatgacaccgctgcccatccattgctcaatggtacagagtgtggggtcagtccaccacccttgacctcccggcagggcaaggtgaggaggcggacccaaagcagtaccagcaggacttgttgccagtgataccaaaacagacttttcccaagcagtgcctcacatgtctgctggtgtggctttgggattctcctgccccacccccccgtccatggcagccccctccccaaggctttgctcacacctgagacaggaaggaggaaggggatccaataggaatatgggccccggaggggaagtcatgcacccccaagccaccaccccccagccttccacgcacatctcctggctggaagagagccctccaaaaaggggacacaggctgccccggcccctcaactgcatccacaccccatcctctcatcttgggtcccagccaggcccccccaaaaccaaagccccctcaagtcctggggtcccagcctgtgcccccagcttcctgcccacccagccctgagcattctcacacagagaaagaacaagcaagggctccagggggacaggatggggcagggcatacagtggggggtgggggggcagctgggaggagggagggacaaaacaaaacattttcctttgggttttttttttctttcttttttctcccctttactctttgggtggtgttgcttttcctttccttttccctttgagatttttttgttgttgtttcctttttgtattttactgatatcaccaggatagtttactctccttctagctttctgcttaccgcacactggataacacacacatacacacccacaaaaatgctcatgaacccaatccggagaaggttccagcaggtcccccaccctcccctcctcctcctacttctcctcttgacagcgaggacaggagggggacaaggggacacctgggcagacccgccggctctccccccaccccaccccgcccctcacatcatactccaatcataaccttgtatattacgcagtcattttggttttcgcggacgcgcctacctaagtaccatttacagaaagtgactctggctgtcattattttgtttatttgttccctatgcaaaaaaaaaatgaaaatgaaaaaagggggattccataaaagattcaataaaagacaaacaaaaaaaaaagaaaaaagaaaaaaatgtataaaaattaaacaagctatgcttcgactcttaaaaaaaaaaaaaaaaaa
//
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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