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7484 WNT9B

7484

WNT9B

Wnt family member 9B

protein-coding

Homo sapiens

基因描述

Type Description
Definition Wnt family member 9B

研究结论

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

名称对应

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

全选

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