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100128927 ZBTB42

100128927

ZBTB42

zinc finger and BTB domain containing 42

protein-coding

Homo sapiens

基因描述

Type Description
Definition zinc finger and BTB domain containing 42

研究结论

Date Results Publications
2015-07-25 10:40:00 ZBTB42 mutation defines a novel lethal congenital contracture syndrome. 25055871
2011-06-18 10:10:00 Data show that ZBTB42 protein is expressed in human skeletal muscle and a murine cell line C2C12 myotubes. 21193930
2010-09-15 22:06:00 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) 20628086
2010-09-15 22:06:00 Observational study of gene-disease association. (HuGE Navigator) 19913121

名称对应

Type IDs
Synonymous LCCS6, ZNF925
Gene
UniProtKB-ID: ZBT42_HUMAN
UniprotKB: B2RXF5
UniParc: UPI0001849D48
EMBL: AL590327, BC157833, BC171822
Ensembl: ENSG00000179627
KO: hsa:100128927
Nucleutide sequences
EMBL-CDS: AAI71822.1, AAI57834.1
Ensembl_TRS: ENST00000342537, ENST00000555360
Protein sequencees
Ensembl_PRO: ENSP00000409107, ENSP00000450673
RefSeq: NP_001131073.1, NP_001357271.1
Others
UniRef100: UniRef100_B2RXF5
UniRef90: UniRef90_B2RXF5
UniRef50: UniRef50_B2RXF5
UniGene: Hs.170853
CCDS: CCDS45174.1

全选

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研究热度

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