abnormal retinol level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the concentration of retinol, which plays an essential role in metabolic functioning of the retina, and growth and differentiation (Mammalian Phenotype Ontology, MP_0011234)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011234
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9 gene mutations causing the abnormal retinol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
LRAT lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
RBP1 retinol binding protein 1, cellular
RBP2 retinol binding protein 2, cellular
RBP4 retinol binding protein 4, plasma
RDH16 retinol dehydrogenase 16 (all-trans)
RHO rhodopsin
SIK3 SIK family kinase 3
STRA6 stimulated by retinoic acid 6
TTR transthyretin