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137902 PXDNL

137902

PXDNL

peroxidasin like

protein-coding

Homo sapiens

基因描述

Type Description
Definition peroxidasin like

研究结论

Date Results Publications
2020-06-20 11:31:00 We also observe evidence for an excess burden of rare, predicted loss-of-function variation in PXDNL and BMS1- two genes relevant to the broader laterality phenotype. These findings highlight potential new genes in the development of laterality defects, and suggest extensive locus heterogeneity and complex genetic models in this class of birth defects. 30622330
2019-02-23 13:33:00 the PMR1 pump, a Golgi resident Ca(2+)/Mn(2+) P-type ATPase, plays a pivotal role in regulating the intracellular levels of calcium and manganese ions. 28780169
2017-06-10 11:28:00 The human PXDN endonuclease stimulates cell motility by down regulating miR-200 family microRNAs. 27257068
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20800603
2010-06-30 22:05:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614

名称对应

Type IDs
Synonymous PMR1, PRM1, VPO2
Gene
UniProtKB-ID: PXDNL_HUMAN
UniprotKB: A1KZ92
UniParc: UPI0001AE6ED6, UPI000049E0C0, UPI0001EC9666
EMBL: CH471068, AK131524, AC090186, AC107374, AY877349, AC012413, EU170240, AK058200, AC011128, AC103958
Ensembl: ENSG00000147485
KO: hsa:137902
Nucleutide sequences
EMBL-CDS: ABX24517.1, BAB71713.1, BAD18663.1, EAW86707.1, AAX70929.1
Ensembl_TRS: ENST00000356297
Protein sequencees
Ensembl_PRO: ENSP00000348645
RefSeq: XP_011515760.1, NP_653252.4, XP_005251225.1, XP_016868530.1
Others
UniRef100: UniRef100_A1KZ92
UniRef90: UniRef90_A1KZ92
UniRef50: UniRef50_A1KZ92
UniGene: Hs.444882
CCDS: CCDS47855.1

全选

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研究热度

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