Protein Rho

URN urn:agi-llid:6010
Total Entities 0
Connectivity 626
Name Rho
Description rhodopsin
Notes Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25% of total cases, approximately 30% of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness. [provided by RefSeq]

Ariadne Ontology Secreted proteins
Biofluids assayable substances

GO Molecular Function retinal binding
metal ion binding
photoreceptor activity
G-protein coupled receptor activity
signal transducer activity

GO Cellular Component membrane
rough endoplasmic reticulum membrane
photoreceptor outer segment membrane
integral to plasma membrane
integral to membrane
plasma membrane
photoreceptor inner segment membrane
photoreceptor inner segment
Golgi apparatus
photoreceptor outer segment

GO Biological Process response to stimulus
signal transduction
phototransduction
G-protein coupled receptor signaling pathway
rhodopsin mediated signaling pathway
red, far-red light phototransduction
phototransduction, visible light
protein-chromophore linkage
protein phosphorylation
cellular response to light stimulus
detection of light stimulus
response to light stimulus
retina development in camera-type eye
sensory perception of light stimulus
visual perception

Pathway Vitamin A (retinol) metabolism and visual cycle
visual phototransduction pathway
retinoid cycle metabolic pathway
retinitis pigmentosa pathway
altered visual phototransduction pathway
altered retinoid cycle metabolic pathway

Group response to stimulus
signal transduction
phototransduction
G-protein coupled receptor signaling pathway
rhodopsin mediated signaling pathway
red, far-red light phototransduction
phototransduction, visible light
protein-chromophore linkage
protein phosphorylation
cellular response to light stimulus
detection of light stimulus
response to light stimulus
retina development in camera-type eye
sensory perception of light stimulus
visual perception
retinal binding
metal ion binding
photoreceptor activity
G-protein coupled receptor activity
signal transducer activity
membrane
rough endoplasmic reticulum membrane
photoreceptor outer segment membrane
integral to plasma membrane
integral to membrane
plasma membrane
photoreceptor inner segment membrane
photoreceptor inner segment
Golgi apparatus
photoreceptor outer segment
Secreted proteins
Biofluids assayable substances

MedScan ID 6010

Hugo ID 10012

Human chromosome position 3q21-q24

GenBank ID NC_000003
NM_000539
NP_000530
NG_009115
NC_018914
AC_000135
AB065668
BAC05894
AC080007
CH471052
EAW79244
S81166
AAB35906
U16824
AAA97436
U49742
AAC31763
BC112104
AAI12105
BC112106
AAI12107
BX537381
CAD97623
P08100
AM392780
CAL37658
BC111451
AAI11452
NC_000072
NM_145383
NP_663358
AC_000028
AC142099
CH466523
EDK99545
EDK99546
M36695
AAA39861
M36696
M36697
M36698
M36699
M55171
AAA63392
AK044333
BAC31871
AK044412
BAC31908
AK164314
BAE37732
BC013125
AAH13125
BC031766
AAH31766
BC094460
P15409
NC_005103
NM_033441
NP_254276
AC_000072
CH473964
EDM02135
EDM02136
U22180
AAA84439
Z46957
CAA87081
P51489
NT_005612
NW_921807
NW_001838884
AC_000046
NT_039353
NW_001030811
Q3TPK4
Q8K0D8
NW_001084832
NW_047696

LocusLink ID 6010
212541
24717

Alias RP4
OPN2
CSNBAD1
rhodopsin
opsin-2
opsin 2, rod pigment
Ops
Noerg1
L opsin
opsin 2
LWS opsin
Red Opsin
Rod Opsin
Long Wavelength Sensitive opsin
Rhodopsin (retinitis pigmentosa 4, autosomal dominant)
Opsin II
retinitis pigmentosa 4, autosomal dominant
rhodopsin (opsin 2, rod pigment) (retinitis pigmentosa 4, autosomal dominan
rhodopsin (opsin 2, rod pigment) (retinitis pigmentosa 4, autosomal dominant)
rhodopsins
visual purple
metarhodopsin II
lumirhodopsin
MGC138309
isorhodopsin
metarhodopsin
metarhodopsin I
metarhodopsins
bathorhodopsin
MGC138311
MGC21585
MGC25387
L opsins

Organism Homo sapiens
Mus musculus
Rattus norvegicus

OMIM ID 180380
610445
136880
613731

Unigene ID Hs.247565
Mm.2965
Mm.406156
Rn.92530

KEGG ID hsa:6010
mmu:212541
rno:24717

Swiss-Prot Accession P08100
P15409
P51489
Q8K0D8
Q96DZ2
Q16414
Q2M249
Q3TPK4

GO ID 0004930
0046872
0009881
0007186
0007603
0006468
0018298
0060041
0016056
0007601
0005794
0005887
0001917
0060342
0001750
0042622
0005886
0016918
0004871
0071482
0009583
0007602
0009585
0009416
0050896
0050953
0007165
0016021
0016020
0030867
0009586
0004872

PIR ID A23665
S51677
A41200

Swiss-Prot ID OPSD_MOUSE
OPSD_RAT
OPSD_HUMAN
Q8K0D8_MOUSE

Cell Localization Membrane

IPI ID IPI00130448
IPI00231956
IPI00027391
IPI00169550
IPI00653892

Mouse chromosome position 6 51.5 cM

Rat chromosome position 4q42

Homologene ID 68068

MGI ID 97914

RGD ID 3573