| Type | Description |
|---|---|
| Definition | WD repeat domain 37 |
| Date | Results | Publications |
|---|---|---|
| 2020-03-21 10:44:00 | Missense Variants in WDR37 Cause a Severe Multisystemic Syndrome. | 31327510 |
| 2020-03-21 10:44:00 | Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. | 31327508 |
| 2010-09-15 22:06:00 | Observational study of gene-disease association. (HuGE Navigator) | 20677014 |
| 2010-06-30 22:05:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
| 2010-06-30 22:05:00 | Meta-analysis and genome-wide association study of gene-disease association. (HuGE Navigator) | 20383146 |
| Type | IDs |
|---|---|
| Gene |
UniProtKB-ID:
WDR37_HUMAN
UniprotKB:
Q9Y2I8
UniParc:
UPI0000E22280,
UPI000013D3B7,
UPI000041ACBB
EMBL:
AL136827,
AB023199,
CH471072,
AK292591,
AC022536,
AL607085,
BC018044
Ensembl:
ENSG00000047056
KO:
hsa:22884
|
| Nucleutide sequences |
EMBL-CDS:
CAB66761.1,
BAA76826.2,
BAF85280.1,
AAH18044.1,
EAW86514.1,
EAW86516.1
Ensembl_TRS:
ENST00000263150,
ENST00000358220
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000350954,
ENSP00000263150
RefSeq:
NP_054742.2
|
| Others |
UniRef100:
UniRef100_Q9Y2I8
UniRef90:
UniRef90_Q9Y2I8
UniRef50:
UniRef50_Q9Y2I8
UniGene:
Hs.188495
CCDS:
CCDS7057.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| 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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