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58524 DMRT3

58524

DMRT3

doublesex and mab-3 related transcription factor 3

protein-coding

Homo sapiens

基因描述

Type Description
Definition doublesex and mab-3 related transcription factor 3

研究结论

Date Results Publications
2018-02-17 10:48:00 Thus, the deletion of the cis-regulatory element for DMRT3 in humans may cause impaired development of the forebrain and gait abnormalities, resulting in spastic CP. In conclusion, this study provides new mechanistic insights into the genetic basis of CP. 29305858
2010-11-13 10:56:00 Chromosome 9p loss is the hallmark of squamous cell carcinoma, and DMRT1, DMRT3 and DOCK8 genes at 9p24.3 might be of interest for the study of the pathophysiology of SCC as potential targets for therapeutic measures. 20596660

名称对应

Type IDs
Synonymous DMRTA3
Gene
UniProtKB-ID: DMRT3_HUMAN
UniprotKB: Q9NQL9
UniParc: UPI0000073634
EMBL: AL136365, AF193873, AJ301581, BC117245, BC113584
Ensembl: ENSG00000064218
KO: hsa:58524
Nucleutide sequences
EMBL-CDS: AAI13585.1, AAF78892.1, CAC37947.1, AAI17246.1
Ensembl_TRS: ENST00000190165
Protein sequencees
Ensembl_PRO: ENSP00000190165
RefSeq: NP_067063.1
Others
UniRef100: UniRef100_Q9NQL9
UniRef90: UniRef90_Q9NQL9
UniRef50: UniRef50_Q9NQL9
UniGene: Hs.189174, Hs.672740, Hs.744394
CCDS: CCDS6443.1

全选

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研究热度

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