Type | Description |
---|---|
Definition | chromodomain helicase DNA binding protein 4 |
Date | Results | Publications |
---|---|---|
2021-03-27 14:43:00 | The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy. | 31474762 |
2021-02-20 13:33:00 | Nucleosome-CHD4 chromatin remodeler structure maps human disease mutations. | 32543371 |
2021-02-13 13:28:00 | NuRD subunit CHD4 regulates super-enhancer accessibility in rhabdomyosarcoma and represents a general tumor dependency. | 32744500 |
2021-02-06 13:51:00 | ZNF410 Uniquely Activates the NuRD Component CHD4 to Silence Fetal Hemoglobin Expression. | 33301730 |
2021-01-30 13:03:00 | [Clinical and genetic analysis of a novel CHD4 gene variant in a Chinese patient with Sifrim-Hitz-Weiss syndrome]. | 33423261 |
Type | IDs |
---|---|
Synonymous | CHD-4, Mi-2b, Mi2-BETA, SIHIWES |
Gene |
UniProtKB-ID:
CHD4_HUMAN,
F5GWX5_HUMAN
UniprotKB:
Q14839,
F5GWX5
UniParc:
UPI000204A9CE,
UPI00001AE66A,
UPI000013C8EF
EMBL:
BC038596,
AC006064,
X86691
Ensembl:
ENSG00000111642
KO:
hsa:1108
|
Nucleutide sequences |
EMBL-CDS:
AAH38596.1,
CAA60384.1
Ensembl_TRS:
ENST00000544040,
ENST00000645095,
ENST00000645022
|
Protein sequencees |
Ensembl_PRO:
ENSP00000440542,
ENSP00000496634,
ENSP00000496163
RefSeq:
NP_001264.2,
NP_001350535.1,
NP_001284482.1
|
Others |
UniRef100:
UniRef100_Q14839,
UniRef100_F5GWX5
UniRef90:
UniRef90_Q14839,
UniRef90_F5GWX5
UniRef50:
UniRef50_Q14839,
UniRef50_Q6PDQ2
UniGene:
Hs.162233
CCDS:
CCDS8552.1
|
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Refseq |
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Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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