Type | Description |
---|---|
Definition | WD repeat domain 11 |
Date | Results | Publications |
---|---|---|
2019-01-19 10:19:00 | Our study reveals a novel class of ciliopathy caused by WDR11 mutations and suggests that CHH/KS may be a part of the human ciliopathy spectrum. | 29263200 |
2018-03-17 12:10:00 | Data indicate a functional link between adaptor protein complex 1 (AP-1) and the WD repeat protein 11 (WDR11) complex. | 29426865 |
2017-10-07 12:02:00 | WDR11 genetic mutation is responsible for the pathophysiology of pituitary stalk interruption syndrome. | 28453858 |
2015-12-12 10:12:00 | Cellular Protein WDR11 Interacts with Specific Herpes Simplex Virus Proteins at the trans-Golgi Network To Promote Virus Replication. | 26178983 |
2010-10-30 10:43:00 | WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome, causing impaired pubertal development. | 20887964 |
Type | IDs |
---|---|
Synonymous | BRWD2, DR11, HH14, SRI1, WDR15 |
Gene |
UniProtKB-ID:
WDR11_HUMAN
UniprotKB:
Q9BZH6
UniParc:
UPI0000138ED1
EMBL:
AB037772,
AL391425,
BC071564,
AC010998,
BC040469,
AF320223
Ensembl:
ENSG00000120008
KO:
hsa:55717
|
Nucleutide sequences |
EMBL-CDS:
AAK08064.1,
AAH71564.1,
AAH40469.1,
BAA92589.2
Ensembl_TRS:
ENST00000263461
|
Protein sequencees |
Ensembl_PRO:
ENSP00000263461
RefSeq:
XP_016871888.1,
NP_060587.8,
XP_016871889.1,
XP_005270020.1,
XP_016871887.1,
XP_024303843.1,
XP_016871886.1
|
Others |
UniRef100:
UniRef100_Q9BZH6
UniRef90:
UniRef90_Q9BZH6
UniRef50:
UniRef50_Q9BZH6
UniGene:
Hs.144447
CCDS:
CCDS7619.1
|
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Refseq |
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