Type | Description |
---|---|
Definition | Wnt family member 10B |
Date | Results | Publications |
---|---|---|
2020-07-11 10:03:00 | No genotype-phenotype correlation is delineated but heterozygous individuals might have mild features of split hand/foot malformation, suggesting a dose-effect of the WNT10B loss-of-function | 31050392 |
2020-02-22 11:59:00 | results suggest a dual role for Wnt family member 10B protein (WNT10B) in normal development and in prostate cancer progression with opposing functions depending on disease stage | 31433503 |
2020-02-15 10:18:00 | Study shows for the first time significant ultraviolet B induced upregulation of WNT7B, WNT10B and TCF7L2 in patients with psoriasis and suggests a potential role of these genes in psoriasis pathogenesis. | 31089877 |
2019-12-14 12:26:00 | Authors define WNT10B-dependent biomarkers for beta-CATENIN/HMGA2/EZH2 signaling predictive of reduced relapse-free survival. | 30563890 |
2019-09-28 11:49:00 | In 7 families afflicted with dental anomalies we detected 4 heterozygous missense variants in WNT10B. We performed whole exome sequencing in the patients who had WNT10B mutations and found no mutations in other known hypodontia-associated genes..They also show that WNT10B variants are associated not only with oligodontia and isolated tooth agenesis, but also with microdontia, short tooth roots, dental pulp stones | 29364501 |
Type | IDs |
---|---|
Synonymous | SHFM6, STHAG8, WNT-12 |
Gene |
UniProtKB-ID:
WN10B_HUMAN
UniprotKB:
O00744
UniParc:
UPI0000138F21,
UPI000050ED7F
EMBL:
X97057,
BC096353,
AK312906,
U81787,
AB070724,
BC096355,
BC096356,
AF028700,
AC073610,
CH471111,
BC096354
Ensembl:
ENSG00000169884
KO:
hsa:7480
|
Nucleutide sequences |
EMBL-CDS:
EAW58028.1,
BAG35752.1,
BAB72181.1,
AAC39549.1,
CAA65769.1,
AAH96355.1,
AAB51685.1,
AAH96356.1,
AAH96354.1,
AAH96353.1
Ensembl_TRS:
ENST00000407467,
ENST00000301061
|
Protein sequencees |
Ensembl_PRO:
ENSP00000301061,
ENSP00000384691
RefSeq:
XP_011537024.1,
XP_011537026.1,
NP_003385.2,
XP_016875408.1,
XP_024304947.1
|
Others |
UniRef100:
UniRef100_O00744
UniRef90:
UniRef90_P48614
UniRef50:
UniRef50_P48614
UniGene:
Hs.91985
CCDS:
CCDS8775.1
|
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