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57480 PLEKHG1

57480

PLEKHG1

pleckstrin homology and RhoGEF domain containing G1

protein-coding

Homo sapiens

基因描述

Type Description
Definition pleckstrin homology and RhoGEF domain containing G1

研究结论

Date Results Publications
2019-11-30 10:58:00 Genetic variation in PLEKHG1 is associated with white matter hyperintensities and ischemic stroke, most strongly with the small vessel subtype, suggesting it acts by promoting small vessel arteriopathy. 30659137
2019-04-27 12:09:00 PLEKHG1 rs9478812 variant substantially increases risk of preeclampsia. 29967039
2010-09-15 22:07:00 Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) 20641033
2010-06-30 22:05:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614
2009-02-11 21:30:00 Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) 19165232

名称对应

Type IDs
Synonymous ARHGEF41
Gene
UniProtKB-ID: PKHG1_HUMAN, Q5JYA6_HUMAN
UniprotKB: Q9ULL1, Q5JYA6
UniParc: UPI000015FC80
EMBL: AL450339, BC151134, BC140864, CH471051, AB033035, AL035086, LS482403
Ensembl: ENSG00000120278
KO: hsa:57480
Nucleutide sequences
EMBL-CDS: BAA86523.1, AAI40865.1, SPT35780.1, EAW47765.1, EAW47766.1, AAI51135.1
Gene_ORFName: hCG_22081
Ensembl_TRS: ENST00000644968, ENST00000358517
Protein sequencees
Ensembl_PRO: ENSP00000496254, ENSP00000351318
RefSeq: NP_001316735.1, NP_001316731.1, NP_001025055.1, NP_001316733.1, NP_001316734.1, NP_001316732.1, NP_001316730.1, NP_001316727.1, NP_001316729.1, NP_001316728.1
Others
UniRef100: UniRef100_Q9ULL1
UniRef90: UniRef90_Q9ULL1
UniRef50: UniRef50_Q9ULL1
UniGene: Hs.189781
CCDS: CCDS34552.1

全选

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研究热度

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