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51384 WNT16

51384

WNT16

Wnt family member 16

protein-coding

Homo sapiens

基因描述

Type Description
Definition Wnt family member 16

研究结论

Date Results Publications
2021-01-16 15:59:00 Short Communication: The Association of WNT16 Polymorphisms with the CD4(+) T Cell Count in the HIV-Infected Population. 31623455
2019-11-30 11:46:00 significant differences in the polymorphisms of the WNT16 rs2908004 genetic variant contributes to the pathogenesis of osteoporosis 31309515
2019-10-19 12:12:00 Study identified two rare variants in functional regions of WNT16 (rs190011371 in WNT16b 3'UTR and rs570754792 in the SOST TATA box) found present in women with low BMD. 30026596
2018-07-21 10:42:00 there was a significant difference in the genotypic frequencies of rs2707466 between hypertrophic and atrophic hip OA in males, with overrepresentation of G alleles in the hypertrophic phenotype. An association in the same direction was observed between these alleles and the type of knee OA, with G alleles being more common in the hypertrophic than in atrophic knee phenotypes 28766055
2017-09-02 12:53:00 WNT16B recognizes cancer cell surface receptors including frizzled (FZD) 3/4/6, a process enhanced by SFRP2, coordinated by the co-receptor LRP6 but subject to abrogation by DKK1. 26751775

名称对应

Type IDs
Gene
UniProtKB-ID: WNT16_HUMAN, E9PH60_HUMAN
UniprotKB: Q9UBV4, E9PH60
UniParc: UPI000013CC77, UPI000002B6DE, UPI000005104C
EMBL: BC104945, AF152584, AC006364, BC104919, AF169963
Ensembl: ENSG00000002745
KO: hsa:51384
Nucleutide sequences
EMBL-CDS: AAI04946.1, AAD49351.1, AAI04920.1, AAD38052.1
Ensembl_TRS: ENST00000222462, ENST00000361301
Protein sequencees
Ensembl_PRO: ENSP00000222462, ENSP00000355065
RefSeq: NP_476509.1, NP_057171.2
Others
UniRef100: UniRef100_Q9UBV4-2, UniRef100_Q9UBV4
UniRef90: UniRef90_Q9UBV4
UniRef50: UniRef50_Q9UBV4
UniGene: Hs.272375
CCDS: CCDS5781.1

全选

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