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145873 MESP2

145873

MESP2

mesoderm posterior bHLH transcription factor 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition mesoderm posterior bHLH transcription factor 2

研究结论

Date Results Publications
2012-09-15 11:12:00 MESP2, HES7 and DUSP6 genes may not be involved in the etiopathogenesis of sporadic and non-syndromic CS in Chinese Han population. 22744456
2010-01-21 00:00:00 Mutated MESP2 causes spondylocostal dysostosis 15122512
2010-01-21 00:00:00 findings suggest a founder-effect mutation in the MESP2 gene as a major cause of the classical Puerto Rican form of spondylothoracic dysostosis/Jarcho-Levin syndrome 18485326
2010-01-21 00:00:00 Mesp1 is down-regulated in the later stages of development by increasing levels of Mesp2 in the wild-type embryo. 16996494

名称对应

Type IDs
Synonymous SCDO2, bHLHc6
Gene
UniProtKB-ID: MESP2_HUMAN
UniprotKB: Q0VG99
UniParc: UPI00006E232B
EMBL: BK000142, AC079075, BC111413
Ensembl: ENSG00000188095
KO: hsa:145873
Nucleutide sequences
EMBL-CDS: DAA00304.1, AAI11414.1
Ensembl_TRS: ENST00000341735
Protein sequencees
Ensembl_PRO: ENSP00000342392
RefSeq: NP_001035047.1
Others
UniRef100: UniRef100_Q0VG99
UniRef90: UniRef90_Q0VG99
UniRef50: UniRef50_O08574
UniGene: Hs.37311
CCDS: CCDS42078.1

全选

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研究热度

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