Home |
Help |
Advanced search
2025-05-09 20:32:33, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001174093 5938 bp mRNA linear PRI 07-JUL-2013 DEFINITION Homo sapiens zinc finger E-box binding homeobox 1 (ZEB1), transcript variant 6, mRNA. ACCESSION NM_001174093 VERSION NM_001174093.1 GI:291575184 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 5938) AUTHORS Lemma,S., Karihtala,P., Haapasaari,K.M., Jantunen,E., Soini,Y., Bloigu,R., Pasanen,A.K., Turpeenniemi-Hujanen,T. and Kuittinen,O. TITLE Biological roles and prognostic values of the epithelial-mesenchymal transition-mediating transcription factors Twist, ZEB1 and Slug in diffuse large B-cell lymphoma JOURNAL Histopathology 62 (2), 326-333 (2013) PUBMED 23190132 REMARK GeneRIF: In diffuse large B-cell lymphoma, cytoplasmic Slug expression was linked to a favourable disease outcome, whereas nuclear expression of ZEB1 indicated an adverse outcome. REFERENCE 2 (bases 1 to 5938) AUTHORS Lechner,J., Dash,D.P., Muszynska,D., Hosseini,M., Segev,F., George,S., Frazer,D.G., Moore,J.E., Kaye,S.B., Young,T., Simpson,D.A., Churchill,A.J., Heon,E. and Willoughby,C.E. TITLE Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation JOURNAL Invest. Ophthalmol. Vis. Sci. 54 (5), 3215-3223 (2013) PUBMED 23599324 REMARK GeneRIF: Missense substitutions in the ZEB1 protein are associated with FECD6 and keratoconus, whereas protein truncating ZEB1 mutations result in PPCD3. Publication Status: Online-Only REFERENCE 3 (bases 1 to 5938) AUTHORS Guo,S., Li,Y., Tong,Q., Gu,F., Zhu,T., Fu,L. and Yang,S. TITLE deltaEF1 down-regulates ER-alpha expression and confers tamoxifen resistance in breast cancer JOURNAL PLoS ONE 7 (12), E52380 (2012) PUBMED 23285017 REMARK GeneRIF: The expression of deltaEF1 is up-regulated by 17beta-estradiol (E2) in MCF-7 cells in an ER-alpha-dependent manner. REFERENCE 4 (bases 1 to 5938) AUTHORS Mehta,J.S., Vithana,E.N., Tan,D.T., Yong,V.H., Yam,G.H., Law,R.W., Chong,W.G., Pang,C.P. and Aung,T. TITLE Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy JOURNAL Invest. Ophthalmol. Vis. Sci. 49 (1), 184-188 (2008) PUBMED 18172091 REMARK GeneRIF: The identification of a novel missense mutation in only one of the patients implied that TCF8 does not play a significant role in the pathogenesis of FECD in this Chinese population. GeneRIF: Observational study of gene-disease association. (HuGE Navigator) REFERENCE 5 (bases 1 to 5938) AUTHORS Manavella,P.A., Roqueiro,G., Darling,D.S. and Cabanillas,A.M. TITLE The ZFHX1A gene is differentially autoregulated by its isoforms JOURNAL Biochem. Biophys. Res. Commun. 360 (3), 621-626 (2007) PUBMED 17610840 REMARK GeneRIF: The Zfhx1a-1 gene is autoregulated in part by negative feedback on its own promoter which is, in turn, modified by the availability of the negative dominant isoform Zfhx1a-2. REFERENCE 6 (bases 1 to 5938) AUTHORS Liskova,P., Tuft,S.J., Gwilliam,R., Ebenezer,N.D., Jirsova,K., Prescott,Q., Martincova,R., Pretorius,M., Sinclair,N., Boase,D.L., Jeffrey,M.J., Deloukas,P., Hardcastle,A.J., Filipec,M. and Bhattacharya,S.S. TITLE Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy JOURNAL Hum. Mutat. 28 (6), 638 (2007) PUBMED 17437275 REMARK GeneRIF: Four novel pathogenic mutations were identified in four families; two deletions, one nonsense, and one duplication within exon 7 in the ZEB1 gene at 10p11.2. Czech patients were genotyped for a founder haplotype and lack of 20p11.2 locus segregation. REFERENCE 7 (bases 1 to 5938) AUTHORS Franklin,A.J., Jetton,T.L., Shelton,K.D. and Magnuson,M.A. TITLE BZP, a novel serum-responsive zinc finger protein that inhibits gene transcription JOURNAL Mol. Cell. Biol. 14 (10), 6773-6788 (1994) PUBMED 7935395 REFERENCE 8 (bases 1 to 5938) AUTHORS Watanabe,Y., Kawakami,K., Hirayama,Y. and Nagano,K. TITLE Transcription factors positively and negatively regulating the Na,K-ATPase alpha 1 subunit gene JOURNAL J. Biochem. 114 (6), 849-855 (1993) PUBMED 8138542 REFERENCE 9 (bases 1 to 5938) AUTHORS Williams,T.M., Montoya,G., Wu,Y., Eddy,R.L., Byers,M.G. and Shows,T.B. TITLE The TCF8 gene encoding a zinc finger protein (Nil-2-a) resides on human chromosome 10p11.2 JOURNAL Genomics 14 (1), 194-196 (1992) PUBMED 1427828 REFERENCE 10 (bases 1 to 5938) AUTHORS Williams,T.M., Moolten,D., Burlein,J., Romano,J., Bhaerman,R., Godillot,A., Mellon,M., Rauscher,F.J. III and Kant,J.A. TITLE Identification of a zinc finger protein that inhibits IL-2 gene expression JOURNAL Science 254 (5039), 1791-1794 (1991) PUBMED 1840704 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DB442432.1, DC299346.1, BC112392.1, AL831979.1, AI086650.1, BX111519.1 and BQ003893.1. Summary: This gene encodes a zinc finger transcription factor. The encoded protein likely plays a role in transcriptional repression of interleukin 2. Mutations in this gene have been associated with posterior polymorphous corneal dystrophy-3 and late-onset Fuchs endothelial corneal dystrophy. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2010]. Transcript Variant: This variant (6) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at an alternate start codon, compared to variant 1. This variant also lacks an in-frame exon in the 5' coding region compared to variant 1. The encoded isoform (c) is shorter and has a distinct N-terminus, compared to isoform a. 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 :: AK091478.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025087, ERS025098 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-24 DB442432.1 1-24 25-47 DC299346.1 1-23 48-322 BC112392.1 1-275 323-3567 BC112392.1 339-3583 3568-5053 AL831979.1 3886-5371 5054-5219 AI086650.1 103-268 c 5220-5353 BX111519.1 1-134 5354-5938 BQ003893.1 8-592 c FEATURES Location/Qualifiers source 1..5938 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="10" /map="10p11.2" gene 1..5938 /gene="ZEB1" /gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3; TCF8; ZFHEP; ZFHX1A" /note="zinc finger E-box binding homeobox 1" /db_xref="GeneID:6935" /db_xref="HGNC:11642" /db_xref="MIM:189909" exon 1..121 /gene="ZEB1" /gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3; TCF8; ZFHEP; ZFHX1A" /inference="alignment:Splign:1.39.8" misc_feature 31..33 /gene="ZEB1" /gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3; TCF8; ZFHEP; ZFHX1A" /note="upstream in-frame stop codon" variation 36 /gene="ZEB1" /gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3; TCF8; ZFHEP; ZFHX1A" /replace="c" /replace="g" /db_xref="dbSNP:367615307" CDS 64..3378 /gene="ZEB1" /gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3; TCF8; ZFHEP; ZFHX1A" /note="isoform c is encoded by transcript variant 6; zinc finger homeodomain enhancer-binding protein; posterior polymorphous corneal dystrophy 3; transcription factor 8 (represses interleukin 2 expression); delta-crystallin enhancer binding factor 1; negative regulator of IL2" /codon_start=1 /product="zinc finger E-box-binding homeobox 1 isoform c" /protein_id="NP_001167564.1" /db_xref="GI:291575185" /db_xref="CCDS:CCDS53506.1" /db_xref="GeneID:6935" /db_xref="HGNC:11642" /db_xref="MIM:189909" /translation="
MADGPRCKRRKQANPRRNNVTNYNTVVETNSDSDDEDKLHIVEEESVTDAADCEGVPEDDLPTDQTVLPGRSSEREGNAKNCWEDDIKDDECESDAENEQNHDPNVEEFLQQQDTAVIFPEAPEEDQRQGTPEASGHDENGTPDAFSQLLTCPYCDRGYKRFTSLKEHIKYRHEKNEDNFSCSLCSYTFAYRTQLERHMTSHKSGRDQRHVTQSGCNRKFKCTECGKAFKYKHHLKEHLRIHSGEKPYECPNCKKRFSHSGSYSSHISSKKCISLIPVNGRPRTGLKTSQCSSPSLSASPGSPTRPQIRQKIENKPLQEQLSVNQIKTEPVDYEFKPIVVASGINCSTPLQNGVFTGGGPLQATSSPQGMVQAVVLPTVGLVSPISINLSDIQNVLKVAVDGNVIRQVLENNQANLASKEQETINASPIQQGGHSVISAISLPLVDQDGTTKIIINYSLEQPSQLQVVPQNLKKENPVATNSCKSEKLPEDLTVKSEKDKSFEGGVNDSTCLLCDDCPGDINALPELKHYDLKQPTQPPPLPAAEAEKPESSVSSATGDGNLSPSQPPLKNLLSLLKAYYALNAQPSAEELSKIADSVNLPLDVVKKWFEKMQAGQISVQSSEPSSPEPGKVNIPAKNNDQPQSANANEPQDSTVNLQSPLKMTNSPVLPVGSTTNGSRSSTPSPSPLNLSSSRNTQGYLYTAEGAQEEPQVEPLDLSLPKQQGELLERSTITSVYQNSVYSVQEEPLNLSCAKKEPQKDSCVTDSEPVVNVIPPSANPINIAIPTVTAQLPTIVAIADQNSVPCLRALAANKQTILIPQVAYTYSTTVSPAVQEPPLKVIQPNGNQDERQDTSSEGVSNVEDQNDSDSTPPKKKMRKTENGMYACDLCDKIFQKSSSLLRHKYEHTGKRPHECGICKKAFKHKHHLIEHMRLHSGEKPYQCDKCGKRFSHSGSYSQHMNHRYSYCKREAEERDSTEQEEAGPEILSNEHVGARASPSQGDSDERESLTREEDEDSEKEEEEEDKEMEELQEEKECEKPQGDEEEEEEEEEVEEEEVEEAENEGEEAKTEGLMKDDRAESQASSLGQKVGESSEQVSEEKTNEA
"
misc_feature 601..669
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/note="Zinc finger, C2H2 type; Region: zf-C2H2; cl15478"
/db_xref="CDD:210117"
misc_feature 721..789
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/note="zinc finger; Region: ZnF_C2H2; smart00355"
/db_xref="CDD:197676"
misc_feature 763..834
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/note="Zinc-finger double domain; Region: zf-H2C2_2;
pfam13465"
/db_xref="CDD:205643"
misc_feature 967..969
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P37275.2); phosphorylation site"
misc_feature 1780..1905
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/note="Homeodomain; DNA binding domains involved in the
transcriptional regulation of key eukaryotic developmental
processes; may bind to DNA as monomers or as homo- and/or
heterodimers, in a sequence-specific manner; Region:
homeodomain; cd00086"
/db_xref="CDD:28970"
misc_feature order(1816..1818,1834..1836,1873..1875,1879..1884,
1891..1896,1900..1905)
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/note="DNA binding site [nucleotide binding]"
/db_xref="CDD:28970"
misc_feature order(1882..1884,1891..1896,1903..1905)
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/note="specific DNA base contacts [nucleotide binding];
other site"
/db_xref="CDD:28970"
misc_feature 1927..1929
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P37275.2); phosphorylation site"
misc_feature 2038..2040
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P37275.2); phosphorylation site"
misc_feature 2107..2109
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphothreonine; propagated from
UniProtKB/Swiss-Prot (P37275.2); phosphorylation site"
misc_feature 2755..2832
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/note="Zinc-finger double domain; Region: zf-H2C2_2;
pfam13465"
/db_xref="CDD:205643"
misc_feature 2839..2916
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/note="Zinc-finger double domain; Region: zf-H2C2_2;
pfam13465"
/db_xref="CDD:205643"
exon 122..322
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/inference="alignment:Splign:1.39.8"
variation 148
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:375120441"
variation 163..165
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="gat"
/db_xref="dbSNP:141941188"
variation 176
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:184444132"
variation 181
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:369331715"
variation 228
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:148639111"
variation 243
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:142039874"
variation 255
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:7918614"
variation 296
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:80194531"
variation 305
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:189276857"
exon 323..484
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/inference="alignment:Splign:1.39.8"
variation 340
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:369476602"
variation 396
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:189111678"
variation 454
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:202218576"
variation 467
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:369587040"
exon 485..687
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/inference="alignment:Splign:1.39.8"
variation 492
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142133469"
variation 594
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:150051354"
variation 606
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:79134358"
variation 613
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:201419824"
exon 688..793
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/inference="alignment:Splign:1.39.8"
variation 698
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:370082712"
variation 699
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:149166539"
variation 792
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:143232269"
exon 794..2604
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/inference="alignment:Splign:1.39.8"
variation 879
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:374468151"
variation 884
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:370663355"
variation 945
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:373826858"
variation 961
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371970352"
variation 969
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:199664973"
variation 1054
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:367672138"
variation 1061
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="t"
/db_xref="dbSNP:148310638"
variation 1084
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:192544989"
variation 1125
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:113838847"
variation 1150
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:142232415"
variation 1206
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:145398072"
variation 1207
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:371431986"
variation 1216
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146384341"
variation 1244
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:138491446"
variation 1252
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:145576217"
variation 1260
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:35238902"
variation 1262
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:75910137"
variation 1267
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:201283071"
variation 1316
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:148867206"
variation 1330
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="t"
/db_xref="dbSNP:150669496"
variation 1424
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:199595565"
variation 1441
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:374398055"
variation 1498
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:139511659"
variation 1529
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:149705490"
variation 1530
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:144430294"
variation 1572
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="a"
/db_xref="dbSNP:35708848"
variation 1609
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:368461324"
variation 1661
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:35753967"
variation 1688
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:140611114"
variation 1704
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:372068000"
variation 1707
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:184880161"
variation 1747
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:143542961"
variation 1755
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="t"
/db_xref="dbSNP:367749817"
variation 1776
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:371536001"
variation 1778
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:375798509"
variation 1797
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:369994958"
variation 1847
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:373879318"
variation 1878
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142143222"
variation 1902
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:201912416"
variation 1906
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:151017318"
variation 1949
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:370211218"
variation 1977
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:151205909"
variation 1980
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:140987489"
variation 1982
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:150228807"
variation 1994
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:141110915"
variation 2037
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:146821579"
variation 2064
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:34846414"
variation 2073
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:35501784"
variation 2082
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="t"
/db_xref="dbSNP:75229306"
variation 2157
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:34111864"
variation 2187
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:200572671"
variation 2198
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:372597335"
variation 2206
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:138456617"
variation 2242
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:117534296"
variation 2254
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:138507868"
variation 2284
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200667415"
variation 2294
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:376963555"
variation 2319
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:143340752"
variation 2321
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:201927623"
variation 2400..2401
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="c"
/db_xref="dbSNP:35905383"
variation 2410
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:148358382"
variation 2414
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1577181"
variation 2419
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:141194628"
variation 2432
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:199944415"
variation 2445
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200125768"
variation 2487
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:201567879"
variation 2522
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:118020901"
variation 2559
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:367685869"
variation 2563
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:139581793"
variation 2591
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:202145455"
exon 2605..2785
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/inference="alignment:Splign:1.39.8"
variation 2620
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:369581136"
variation 2671
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:143370284"
variation 2675
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:369330183"
variation 2693
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:35653460"
variation 2706
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:147142042"
variation 2710
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:184220160"
variation 2717
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:78449005"
exon 2786..5928
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/inference="alignment:Splign:1.39.8"
variation 2797
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:370801976"
variation 2855
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:374536300"
variation 2890
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:149757409"
variation 2901
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:145553237"
variation 2973
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:376922710"
variation 2986
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:371696203"
variation 3034
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:148446855"
variation 3048
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:200948247"
variation 3056
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200238558"
variation 3064
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:142629102"
variation 3069
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146803682"
variation 3093
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:140617391"
variation 3095
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="t"
/db_xref="dbSNP:145633572"
variation 3174
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:146561222"
variation 3193..3195
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="gaa"
/db_xref="dbSNP:375988551"
variation 3195..3197
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="aga"
/db_xref="dbSNP:370699695"
variation 3196..3198
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="gag"
/db_xref="dbSNP:369270839"
variation 3230
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="t"
/db_xref="dbSNP:375270538"
variation 3232
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:146672684"
variation 3244
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:140217290"
variation 3260
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:201845244"
variation 3290
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="t"
/db_xref="dbSNP:141086946"
variation 3303
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:34256798"
variation 3311
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:150279725"
variation 3316
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:138952579"
variation 3334
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:143438972"
variation 3391
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:188563673"
variation 3424
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:113977142"
variation 3428
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:374867798"
STS 3436..3586
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/standard_name="D10S1781"
/db_xref="UniSTS:34015"
variation 3447
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:78595841"
STS 3456..3672
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/standard_name="SHGC-31480"
/db_xref="UniSTS:26889"
variation 3526..3527
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="ac"
/db_xref="dbSNP:143911186"
variation 3527..3528
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="ac"
/db_xref="dbSNP:72221464"
variation 3552..3557
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="cacaca"
/db_xref="dbSNP:36207630"
variation 3554..3559
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="cacaca"
/db_xref="dbSNP:5784248"
variation 3555..3558
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="acac"
/db_xref="dbSNP:10610992"
variation 3557..3562
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="acacac"
/db_xref="dbSNP:3086583"
variation 3564..3567
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="caca"
/db_xref="dbSNP:60354357"
variation 3567..3568
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="tg"
/db_xref="dbSNP:71027030"
variation 3644
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:372557668"
variation 3721
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:148015830"
variation 3732
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:372771766"
variation 3764
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:141676377"
variation 3782
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:10490929"
variation 4061..4064
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="actc"
/db_xref="dbSNP:376070628"
variation 4220
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:150246922"
variation 4272..4279
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="gtattttc"
/db_xref="dbSNP:368007808"
variation 4334
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:193087933"
variation 4359
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:139194135"
variation 4687
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:185686910"
variation 4752..4753
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="tg"
/db_xref="dbSNP:149726475"
variation 4935
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="t"
/db_xref="dbSNP:118189529"
variation 5009
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:2839667"
variation 5015
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:191505587"
variation 5091
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:7349"
variation 5159
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:183651581"
variation 5163
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="c"
/db_xref="dbSNP:188702835"
variation 5344
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:77992406"
variation 5396
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:75678706"
variation 5438..5439
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace=""
/replace="t"
/db_xref="dbSNP:201215623"
variation 5517
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="g"
/replace="t"
/db_xref="dbSNP:143336093"
variation 5547
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:75717753"
variation 5591
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:147527127"
variation 5593
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:200534090"
variation 5711
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:181434712"
variation 5749
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="t"
/db_xref="dbSNP:220071"
variation 5793
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="a"
/replace="g"
/db_xref="dbSNP:184147533"
variation 5798
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
/replace="c"
/replace="g"
/db_xref="dbSNP:190131604"
polyA_signal 5897..5902
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
polyA_site 5928
/gene="ZEB1"
/gene_synonym="AREB6; BZP; DELTAEF1; FECD6; NIL2A; PPCD3;
TCF8; ZFHEP; ZFHX1A"
ORIGIN
gggggggaagggggagggagggggaggaggtgactcgagcatttagacacaagcgagaggatcatggcggatggccccaggtgtaagcgcagaaagcaggcgaacccgcggcgcaataacgttacaaattataatactgtggtagaaacaaattcagattcagatgatgaagacaaactgcatattgtggaagaagaaagtgttacagatgcagctgactgtgaaggtgtaccagaggatgacctgccaacagaccagacagtgttaccagggaggagcagtgaaagagaagggaatgctaagaactgctgggaggatgacataaaagatgatgaatgcgagtcagatgcagaaaatgagcaaaaccatgatcctaatgttgaagagtttctacaacaacaagacactgctgtcatttttcctgaggcacctgaagaggaccagaggcagggcacaccagaagccagtggtcatgatgaaaatggaacaccagatgcattttcacaattactcacctgtccatattgtgatagaggctataaacgctttacctctctgaaagaacacattaaatatcgtcatgaaaagaatgaagataactttagttgctccctgtgcagttacacctttgcatacagaacccaacttgaacgtcacatgacatcacataaatcaggaagagatcaaagacatgtgacgcagtctgggtgtaatcgtaaattcaaatgcactgagtgtggaaaagctttcaaatacaaacatcacctaaaagagcacttaagaattcacagtggagagaagccatatgaatgcccaaactgcaagaaacgcttttcccattctggctcctatagctcacacataagcagtaagaaatgtatcagcttgatacctgtgaatgggcgaccaagaacaggactcaagacatctcagtgttcttcaccgtctctttcagcatcaccaggcagtcccacacgaccacagatacggcaaaagatagagaataaaccccttcaagaacaactttctgttaaccaaattaaaactgaacctgtggattatgaattcaaacccatagtggttgcttcaggaatcaactgttcaacccctttacaaaatggggttttcactggtggtggcccattacaggcaaccagttctcctcagggcatggtgcaagctgttgttctgccaacagttggtttggtgtctcccataagtatcaatttaagtgatattcagaatgtacttaaagtggcggtagatggtaatgtaataaggcaagtgttggagaataatcaagccaatcttgcatccaaagaacaagaaacaatcaatgcttcacccatacaacaaggtggccattctgttatttcagccatcagtcttcctttggttgatcaagatggaacaaccaaaattatcatcaactacagtcttgagcagcctagccaacttcaagttgttcctcaaaatttaaaaaaagaaaatccagtcgctacaaacagttgtaaaagtgaaaagttaccagaagatcttactgttaagtctgagaaggacaaaagctttgaagggggggtgaatgatagcacttgtcttctgtgtgatgattgtccaggagatattaatgcacttccagaattaaagcactatgacctaaagcagcctactcagcctcctccactccctgcagcagaagctgagaagcctgagtcctctgtttcatcagctactggagatggcaatttgtctcctagtcagccacctttaaagaacctcttgtctctcctaaaagcatattatgctttgaatgcacaaccaagtgcagaagagctctcaaaaattgctgattcagtaaacctaccactggatgtagtaaaaaagtggtttgaaaagatgcaagctggacagatttcagtgcagtcttctgaaccatcttctcctgaaccaggcaaagtaaatatccctgccaagaacaatgatcagcctcaatctgcaaatgcaaatgaaccccaggacagcacagtaaatctacaaagtcctttgaagatgactaactccccagttttaccagtgggatcaaccaccaatggttccagaagtagtacaccatccccatcacctctaaacctttcctcatccagaaatacacagggttacttgtacacagctgagggtgcacaagaagagccacaagtagaacctcttgatctttcactaccaaagcaacagggagaattattagaaaggtcaactatcactagtgtttaccagaacagtgtttattctgtccaggaagaacccttgaacttgtcttgcgcaaaaaaggagccacaaaaggacagttgtgttacagactcagaaccagttgtaaatgtaatcccaccaagtgccaaccccataaatatcgctatacctacagtcactgcccagttacccacaatcgtggccattgctgaccagaacagtgttccatgcttaagagcgctagctgccaataagcaaacgattctgattccccaggtggcatacacctactcaactacggtcagccctgcagtccaagaaccacccttgaaagtgatccagccaaatggaaatcaggatgaaagacaagatactagctcagaaggagtatcaaatgtagaggatcagaatgactctgattctacaccgcccaaaaagaaaatgcggaagacagaaaatggaatgtatgcttgtgatttgtgtgacaagatattccaaaagagtagttcattattgagacataaatatgaacacacaggtaaaagacctcatgagtgtggaatctgtaaaaaggcatttaaacacaaacatcatttgattgaacacatgcgattacattctggagaaaagccctatcaatgtgacaaatgtggaaagcgcttctcacactctgggtcttattctcaacacatgaatcatcgctactcctactgtaagagagaagcggaagaacgtgacagcacagagcaggaagaggcagggcctgaaatcctctcgaatgagcacgtgggtgccagggcgtctccctcacagggcgactcggacgagagagagagtttgacaagggaagaggatgaagacagtgaaaaagaggaagaggaggaggataaagagatggaagaattgcaggaagaaaaagaatgtgaaaaaccacaaggggatgaggaagaggaggaggaggaggaagaagtggaagaagaagaggtagaagaggcagagaatgagggagaagaagcaaaaactgaaggtctgatgaaggatgacagggctgaaagtcaagcaagcagcttaggacaaaaagtaggcgagagtagtgagcaagtgtctgaagaaaagacaaatgaagcctaatcgtttttctagaaggaaaataaattctaattgataatgaatttcgttcaatattatccttgcttttcatggaaacacagtaacctgtatgctgtgattcctgttcactactgtgtaaagtaaaaactaaaaaaatacaaaatacaaaacacacacacacacacacacacacacacacacacacacacaaaataaatccgggtgtgcctgaacctcagacctagtaatttttcatgcagttttcaaagttaggaacaagtttgtaacatgcagcagattagaaaaccttaatgactcagagagcaacaatacaagaggttaaaggaagctgattaattagatatgcatctggcattgttttatcttatcagtattatcactcttatgttggtttattcttaagctgtacaattgggagaaattttataattttttattggtaaacatatgctaaatccgcttcagtattttattatgttttttaaaatgtgagaacttctgcactacaaaattcccttcacagagaagtataatgtagttccaacccgtgctaactaccttttataaattcagtctagaaggtagtaatttctaatatttagatgtcttagtagagcgtattatcatttaaagtgtattgttagccttaagaaagcagctgatagaagaactgaagtttcttactcacgtggtttaaaatggagttcaaaagattgccattgagttctgattgcagggactaacaatgttaatctgataaggacagcaaaatcatcagaatcagtgtttgtgattgtgtttgaatatgtggtaacatatgaaggatatgacatgaagctttgtatctcctttggccttaagcaagacctgtgtgctgtaagtgccatttctcagtattttcaaggctctaacccgccttcatccaatgtgtggcctacaataactagcatttgttgatttgtctcttgtatcaaaattcccaaataaaacttaaaaccactgactctgtcagagaaactgaaacactgggacatttcatccttcaattcctcggtattgattttatgttgattgattttcagaatttctctacagaaacgaaagggaaattttctaatctgctttatccatgtacttgcatttcagacatggacatgctattgttatttggctcataactgtttccaaatgttagttattatggacccaatttattaacaacattagctgatttttacctatcagtattattttatttcttttagtttatagatctgtgcaacatttttgtactgtatgtcttcaaacctggcagtattaatacccttcttactgacatatgtacttttagttttagaaaacttttatatttatgtgtcttatttttatatttctttatttattacacagtgtagtgtataatactgtagtttgtattaatacaataatatattttagtatgaaaatttggaaagttgataagatttaaagtagagatgcaattggttctcctgcattgagatttgatttaacagtgttatgttaacatttatacttgccttggactgtagaacagaacttaaatgggaatgtattagttttacaactacaatcaagtcattttacctttacccagtttttaatataaaacttaaattttgaaattcactgtgtgactaatagcatgatgctctgcagttttattaagaaatcagcctaaccatacaactctcatttccttagtaagccaaattaggattaacttctataaacagtgttgggaacaatgtttaacattttgtgccaatttgttcctgtattcatgtatgtaagttacagatctgactcttcatttttaagttccttgttacatcatggtcattttctagttttttaccagactcccatctcacaataaaatgcatcaacaagcctgaactgctgtcattcttttcatcattatcagtattttctttggaaaactgtgaaatggggtacattgtcatcctgcatttgattcatcttgagctgaatttgggtaacactaaatgttttagacattctccactaaattatggattttcttgtggctaaatgtttctggagaggtcagagttgacaaaacctcttcacaggttgctccttcttcctgaaatccttaatcctccgcatttcatgcttcaggtcatttcagggaagcctgggtttagatgcctttctgactctcagctcctgcacttctgtcatcatacctctgatactattatttatattccttccccactaggaacaggaaccacatttgtcatagtcactctcacattcctcactgcctaacagggtgcctggcataagttgggacaacagatatttgttgaataaaaatataatttgcatgtttatggagctcagctatgttctcactttttttgcttctaattccagaatatatgttaaatgatctaataatttgattattttcttataagtcttattaaacactagtcataatagacacaataaattatgccttctttttctattgccttaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:6935 -> Molecular function: GO:0003682 [chromatin binding] evidence: IEA
GeneID:6935 -> Molecular function: GO:0003690 [double-stranded DNA binding] evidence: IEA
GeneID:6935 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IEA
GeneID:6935 -> Molecular function: GO:0003713 [transcription coactivator activity] evidence: TAS
GeneID:6935 -> Molecular function: GO:0003714 [transcription corepressor activity] evidence: TAS
GeneID:6935 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:6935 -> Molecular function: GO:0008134 [transcription factor binding] evidence: IEA
GeneID:6935 -> Molecular function: GO:0008270 [zinc ion binding] evidence: TAS
GeneID:6935 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IEA
GeneID:6935 -> Molecular function: GO:0070888 [E-box binding] evidence: ISS
GeneID:6935 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IEA
GeneID:6935 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
GeneID:6935 -> Biological process: GO:0006357 [regulation of transcription from RNA polymerase II promoter] evidence: TAS
GeneID:6935 -> Biological process: GO:0006955 [immune response] evidence: TAS
GeneID:6935 -> Biological process: GO:0007389 [pattern specification process] evidence: IEA
GeneID:6935 -> Biological process: GO:0008283 [cell proliferation] evidence: TAS
GeneID:6935 -> Biological process: GO:0008285 [negative regulation of cell proliferation] evidence: IEA
GeneID:6935 -> Biological process: GO:0010464 [regulation of mesenchymal cell proliferation] evidence: IEA
GeneID:6935 -> Biological process: GO:0014823 [response to activity] evidence: IEA
GeneID:6935 -> Biological process: GO:0017015 [regulation of transforming growth factor beta receptor signaling pathway] evidence: IEA
GeneID:6935 -> Biological process: GO:0030857 [negative regulation of epithelial cell differentiation] evidence: IEA
GeneID:6935 -> Biological process: GO:0030900 [forebrain development] evidence: IEA
GeneID:6935 -> Biological process: GO:0031667 [response to nutrient levels] evidence: IEA
GeneID:6935 -> Biological process: GO:0033081 [regulation of T cell differentiation in thymus] evidence: IEA
GeneID:6935 -> Biological process: GO:0045666 [positive regulation of neuron differentiation] evidence: ISS
GeneID:6935 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IDA
GeneID:6935 -> Biological process: GO:0045892 [negative regulation of transcription, DNA-dependent] evidence: IMP
GeneID:6935 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IEA
GeneID:6935 -> Biological process: GO:0048596 [embryonic camera-type eye morphogenesis] evidence: IEA
GeneID:6935 -> Biological process: GO:0048704 [embryonic skeletal system morphogenesis] evidence: IEA
GeneID:6935 -> Biological process: GO:0048752 [semicircular canal morphogenesis] evidence: IEA
GeneID:6935 -> Biological process: GO:0051150 [regulation of smooth muscle cell differentiation] evidence: IEA
GeneID:6935 -> Biological process: GO:0051216 [cartilage development] evidence: IEA
GeneID:6935 -> Biological process: GO:0071230 [cellular response to amino acid stimulus] evidence: IEA
GeneID:6935 -> Biological process: GO:0071560 [cellular response to transforming growth factor beta stimulus] evidence: IEA
GeneID:6935 -> Biological process: GO:0090103 [cochlea morphogenesis] evidence: IEA
GeneID:6935 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:6935 -> Cellular component: GO:0005667 [transcription factor complex] evidence: IEA
GeneID:6935 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
GeneID:6935 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.