abnormal vitamin a level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the concentration of any of the vitamin A compounds, retinol, retinal (retinaldehyde) and retinoic acid; animals can not synthesize vitamin A de novo, but form it through oxidative cleavage of carotenoids supplied in the diet (Mammalian Phenotype Ontology, MP_0011232)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011232
Similar Terms
Downloads & Tools

Genes

14 gene mutations causing the abnormal vitamin a level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
ADH7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide
BCO1 beta-carotene oxygenase 1
DGAT1 diacylglycerol O-acyltransferase 1
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
RBP7 retinol binding protein 7, cellular
RDH16 retinol dehydrogenase 16 (all-trans)
RHO rhodopsin
SIK3 SIK family kinase 3
STRA6 stimulated by retinoic acid 6
TTR transthyretin