abnormal retinol metabolism Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description altered ability to metabolize retinol, which plays an essential role in metabolic functioning of the retina, and growth of and differentiation (Mammalian Phenotype Ontology, MP_0005444)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005444
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5 gene mutations causing the abnormal retinol metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADH1C alcohol dehydrogenase 1C (class I), gamma polypeptide
ADH7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide
DHRS3 dehydrogenase/reductase (SDR family) member 3
RBP1 retinol binding protein 1, cellular
TTR transthyretin