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1106 CHD2

1106

CHD2

chromodomain helicase DNA binding protein 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition chromodomain helicase DNA binding protein 2

研究结论

Date Results Publications
2021-04-03 13:34:00 CHD2-Related CNS Pathologies. 33435571
2020-07-04 10:16:00 Study finds that Q1392TfsX17 maybe the hot-spot mutation of CHD2 and that West syndrome could be a new phenotype of CHD2 mutation. 31677157
2020-03-07 11:19:00 CHD2 encodes a member of the chromodomain helicase DNA-binding (CHD) family involved in chromatin remodeling. This observation adds schizophrenia to the phenotypic spectrum of chromodomain remodeling disorders, which may lead to innovative therapeutic approaches. 31914951
2019-06-01 12:26:00 DNA helicases CHD2 and CHD7 could reduce BAP1 promoter activity, likely through unwinding its G4 structures. 29787736
2019-05-25 10:57:00 CHD2 mutation is associated with neurodevelopmental disorders. 29740950

名称对应

Type IDs
Synonymous EEOC
Gene
UniProtKB-ID: CHD2_HUMAN
UniprotKB: O14647
UniParc: UPI000006EF54, UPI00001AEF2D, UPI0000E8A85C
EMBL: CH471101, BC007347, AF006514, BT007050, AC013394, CR978407, FJ515838
Ensembl: ENSG00000173575
KO: hsa:1106
Nucleutide sequences
EMBL-CDS: EAX02160.1, AAH07347.1, AAP35699.1, AAB87382.1, ACS13730.1
Ensembl_TRS: ENST00000626874, ENST00000420239, ENST00000394196
Protein sequencees
Ensembl_PRO: ENSP00000377747, ENSP00000406581, ENSP00000486629
RefSeq: NP_001036037.1, NP_001262.3
Others
UniRef100: UniRef100_O14647
UniRef90: UniRef90_O14647
UniRef50: UniRef50_O14647
UniGene: Hs.220864
CCDS: CCDS45356.1, CCDS10374.2

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