Type | Description |
---|---|
Definition | pleckstrin homology and RhoGEF domain containing G1 |
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 |
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
|
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Refseq |
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