Type | Description |
---|---|
Definition | chromodomain helicase DNA binding protein 2 |
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 |
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
|