Type | Description |
---|---|
Definition | Wnt family member 9B |
Date | Results | Publications |
---|---|---|
2021-04-03 13:32:00 | Canonical Wnts Mediate CD8(+) T Cell Noncytolytic Anti-HIV-1 Activity and Correlate with HIV-1 Clinical Status. | 32887752 |
2021-02-13 13:22:00 | Circulating Exosomal miR-20b-5p Inhibition Restores Wnt9b Signaling and Reverses Diabetes-Associated Impaired Wound Healing. | 31867895 |
2018-02-03 11:22:00 | Our study further supports the involvement of WNT9B as a cleft susceptibility gene in Brazilian families experiencing NSCL+/-P. Although additional studies are still necessary to unveil the exact mechanism by which WNT genes would contribute to NSCL+/-P, allelic polymorphisms in these genes and their interactions may partly explain the variance of individual susceptibility to NSCL+/-P. | 24437584 |
2017-10-14 13:10:00 | Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype | 28915250 |
2016-05-07 11:06:00 | This association study successfully identified two susceptibility (WNT9B and PBX1) associated with Mayer-Rokitansky-Kuster-Hauser syndrome risk, both separately and interactively. | 26075712 |
Type | IDs |
---|---|
Synonymous | WNT14B, WNT15 |
Gene |
UniProtKB-ID:
WNT9B_HUMAN,
E7EPC3_HUMAN
UniprotKB:
O14905,
E7EPC3
UniParc:
UPI000013DFB5,
UPI000040AE77
EMBL:
AC019319,
AB063483,
AC015855,
KC877662,
AY358217,
AF028703,
AC243685
Ensembl:
ENSG00000276799,
ENSG00000158955
KO:
hsa:7484
|
Nucleutide sequences |
EMBL-CDS:
AAC39551.1,
BAB70499.1,
AAQ88584.1
Gene_ORFName:
UNQ6973/PRO21956
Ensembl_TRS:
ENST00000613753,
ENST00000290015,
ENST00000393461,
ENST00000633488
|
Protein sequencees |
Ensembl_PRO:
ENSP00000482127,
ENSP00000290015,
ENSP00000377105,
ENSP00000488518
RefSeq:
NP_003387.1,
XP_011523480.1,
NP_001307387.1
|
Others |
UniRef100:
UniRef100_E7EPC3,
UniRef100_O14905
UniRef90:
UniRef90_O35468,
UniRef90_A0A2K5PDZ7
UniRef50:
UniRef50_B6V3E1,
UniRef50_O35468
UniGene:
Hs.326420
CCDS:
CCDS11506.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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