RDH13 Products

Description

The RDH13 gene encodes a mitochondrial short-chain dehydrogenase/reductase, which catalyzes the reduction and oxidation ofretinoids. The encoded enzyme may function in retinoic acid production and may also protect the mitochondria againstoxidative stress. Alte

Bioinformatics

Entrez	112724 Human
Uniprot	NP_612421 Human NP_612421.1 Human
Product By Gene ID	112724
Alternate Names	EC 1.1.1.- DKFZp313H0740 short chain dehydrogenase/reductase family 7C, member 3 retinol dehydrogenase 13 (all-trans and 9-cis) retinol dehydrogenase 13 SDR7C3 FLJ39479 retinol dehydrogenase 13 (all-trans/9-cis)

Diseases related to RDH13

Discover more about diseases related to RDH13.

Exophthalmos
Strabismus
Esotropia
Blind Vision
Amaurosis
Leber Congenital Amaurosis
Retinal Degeneration
Radiation Injuries, Experimental
Lymphoma
B-cell Lymphomas
Retinal Diseases
Optic Atrophy, Hereditary, Leber

Pathways for RDH13

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Localization
Transport
Regeneration
Cell Proliferation
Vitellogenesis
Cell Death
Electron Transport
Electron Transport Chain
Pathogenesis

Research Areas for RDH13

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Lipid and Metabolism

PTMs for RDH13

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Cleavage
Oxidation

Bioinformatics Tool for RDH13

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