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65266 WNK4

65266

WNK4

WNK lysine deficient protein kinase 4

protein-coding

Homo sapiens

基因描述

Type Description
Definition WNK lysine deficient protein kinase 4

研究结论

Date Results Publications
2020-05-30 10:10:00 D564N mutation in WNK4 is a novel genetic cause of PHA2 with a relatively mild phenotype. 31044551
2020-02-29 11:41:00 Molecular dynamics simulations indicate the effects of these mutations on the interaction between the Kelch domain of kelch-like protein 3 (KLHL3) and the acidic motif (AM) of WNK lysine deficient protein kinase 4 protein (WNK4). 30931564
2019-11-02 12:12:00 This study has identified specific WNK4 that are involved in opening TRPV4, using a selective screen of short interfering ribonucleic acid (siRNA) SMARTpools, which individually targeted all human kinases, in human embryonic kidney 293 (HEK293) cells that stably express inducible TRPV4. 29148820
2019-07-13 11:40:00 Kidney-specific WNK1 isoform is a potent activator of WNK4 and NCC-mediated sodium/chloride transport. 29846116
2019-05-04 11:41:00 tacrolimus increases levels of KLHL3(S433-P), resulting in increased levels of WNK4, phosphorylated and Na-Cl cotransporter.These findings demonstrate that KLHL3(S433-P) is a calcineurin substrate and implicate increased KLHL3 phosphorylation in tacrolimus-induced pathologies. 30718414

名称对应

Type IDs
Synonymous PHA2B, PRKWNK4
Gene
UniProtKB-ID: WNK4_HUMAN
UniprotKB: Q96J92
UniParc: UPI000006FC0F, UPI0000236D78, UPI0000236D79
EMBL: EU332870, AK096003, AK096052, AJ316534, AF390018, CH471152, BC136664, AJ309861
Ensembl: ENSG00000126562
KO: hsa:65266
Nucleutide sequences
EMBL-CDS: EAW60881.1, BAC04669.1, BAC04688.1, AAK91995.1, ABY87559.1, EAW60882.1, CAC32991.1, AAI36665.1, CAC48387.1
Ensembl_TRS: ENST00000246914
Protein sequencees
Ensembl_PRO: ENSP00000246914
RefSeq: NP_001308228.1, NP_115763.2, XP_016880451.1, XP_016880455.1
Others
UniRef100: UniRef100_Q96J92
UniRef90: UniRef90_Q96J92
UniRef50: UniRef50_Q96J92
UniGene: Hs.105448
CCDS: CCDS11439.1

全选

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