RDH5 A294P

Stable Identifier
R-HSA-2471966
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
11-cis retinol dehydrogenase 5, RDH5 Ala294Pro
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
RDH5, HSD17B9, RDH1, SDR9C5
Chain
signal peptide:1-23, chain:24-318
Other Identifiers
0002850541
00280+1.1.1.31
11724965_at
11724966_s_at
210106_at
32727_at
3416922
3416924
3416925
3416926
3416927
3416930
3416932
3416934
3416935
3416936
5959
63345
7956018
A0A024RB18
CCDS31829
ENSG00000135437
ENSP00000257895
ENSP00000447128
ENST00000257895
ENST00000548082
EntrezGene:5959
g1616653_3p_at
GE54293
GO:0001523
GO:0004745
GO:0005783
GO:0005788
GO:0005789
GO:0007601
GO:0016020
GO:0016491
GO:0042572
GO:0044297
GO:0050896
GO:0055114
HGNC:9940
HPA063345
Hs.600940
ILMN_1773395
MIM:136880
MIM:601617
NM_001199771
NM_002905
NP_001186700
NP_002896
PF00106
PR00080
PR00081
PWY-6861
RDH5
RDH5-201
RDH5-204
U89717_at
uc001shk.4
uc001shl.4
UPI0000034C0B
Participant Of
Other forms of this molecule
Modified Residues
Name
L-alanine 294 replaced with L-proline
Coordinate
294
PsiMod HEY
A protein modification that effectively converts a source amino acid residue to L-proline.
A protein modification that effectively removes or replaces an L-alanine.
Disease
Name Identifier Synonyms
fundus albipunctatus 11105 Pigmentary retinal dystrophy, Pigmentary retinal dystrophy (disorder)
Cross References
Brenda
GeneCards
PRO
Orphanet
HMDB Protein
Interactors (1)
Accession #Entities Entities Confidence Score Evidence (IntAct)
 UniProt:O43929 ORC4  1 0.488 2