Retinoid metabolism in retina: healthy vs. RLBP1-deficient (Homo sapiens)
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Description
RLBP1 encodes CRALBP, a cellular retinaldehyde-binding protein that functions as a soluble retinoid carrier in the visual cycle of the eye. Mutations in RLBP1 are linked to recessively inherited conditions, such as Bothnia dystrophy, retinitis pigmentosa, retinitis punctata albescens, fundus albipunctatus, and Newfoundland rod-cone dystrophy.
Quality Tags
Ontology Terms
Pathway Ontology : vascular endothelial growth factor signaling pathway
Cell Type : endothelial cell
Bibliography
- Schlegel DK, Ramkumar S, von Lintig J, Neuhauss SC; ''Disturbed retinoid metabolism upon loss of rlbp1a impairs cone function and leads to subretinal lipid deposits and photoreceptor degeneration in the zebrafish retina.''; Elife, 2021 PubMed Europe PMC Scholia
History
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External references
DataNodes
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Name ![]() | Type ![]() | Database reference ![]() | Comment ![]() |
---|---|---|---|
11cisRAL | Metabolite | CHEBI:16066 (ChEBI) ![]() | |
11cisRE | Metabolite | CHEBI:195358 (ChEBI) ![]() | |
11cisROL | Metabolite | CHEBI:46856 (ChEBI) ![]() | |
RLBP1 | GeneProduct | ENSG00000140522 (Ensembl) ![]() | "Cralbpa" in source |
atRAL | Metabolite | CHEBI:17898 (ChEBI) ![]() | |
atRE | Metabolite | CHEBI:63410 (ChEBI) ![]() | |
atROL | Metabolite | CHEBI:17336 (ChEBI) ![]() |
Annotated Interactions
No annotated interactions