Type | Description |
---|---|
Definition | retinal G protein coupled receptor |
Date | Results | Publications |
---|---|---|
2019-05-11 11:03:00 | The clinical data suggest a variable and slow degeneration of the RPE. A shared chromosomal segment surrounding the RGR gene suggests a single ancestral mutational event underlying all three families. | 30347075 |
2018-11-17 11:53:00 | The results indicate that the cone photoreceptors of humans and cattle express a nonvisual opsin of the Go/RGR or tetraopsin group. | 30034210 |
2017-06-10 12:15:00 | study to systemically analyze the potential role of variants of RGR in retinal diseases results of the suggested that the heterozygous truncation variants in RGR were less likely to be pathogenic | 27748892 |
2011-10-15 11:30:00 | conclude that the ability of hRgr to activate both Ral and Ras is responsible for its transformation-inducing phenotype and it could be an important contributor in the development of some T-cell malignancies | 21441953 |
2011-01-22 10:28:00 | It is likely that mutations in RGR, RBP3, and possibly RBP1 occur rarely in inherited retinal dystrophies. | 21067480 |
Type | IDs |
---|---|
Synonymous | RP44 |
Gene |
UniProtKB-ID:
RGR_HUMAN,
A0A0S2Z498_HUMAN,
A0A0S2Z494_HUMAN
UniprotKB:
P47804,
A0A0S2Z498,
A0A0S2Z494
UniParc:
UPI0000148530,
UPI0000050433,
UPI0000072293
EMBL:
KU178307,
U15789,
BC011349,
U15788,
U15786,
U15785,
U15790,
AC022389,
U14911,
BG912392,
U15787,
U14910,
KU178308,
CH471142
Ensembl:
ENSG00000148604
KO:
hsa:5995
|
Nucleutide sequences |
EMBL-CDS:
AAH11349.1,
AAA56748.1,
AAB92384.1,
ALQ33765.1,
EAW80354.1,
ALQ33766.1
Gene_ORFName:
hCG_20085
Ensembl_TRS:
ENST00000358110,
ENST00000359452,
ENST00000652092
|
Protein sequencees |
Ensembl_PRO:
ENSP00000498299,
ENSP00000350823,
ENSP00000352427
RefSeq:
NP_002912.2,
NP_001012740.1,
XP_024303886.1,
NP_001012738.1
|
Others |
UniRef100:
UniRef100_A0A494BZT6,
UniRef100_P47804,
UniRef100_P47804-2
UniRef90:
UniRef90_A0A2I3HX40,
UniRef90_P47804-2,
UniRef90_P47804
UniRef50:
UniRef50_Q28EK0,
UniRef50_P47804,
UniRef50_P47804-2
UniGene:
Hs.1544
CCDS:
CCDS41543.1,
CCDS7374.1
|
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