disorganized photoreceptor inner segment Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description derangement of the pattern of the photoreceptor region which contains the machinery of the cell (mitochondria, golgi, endoplasmic reticulum, etc) and where opsin molecules are assembled and passed to be part of the outer segment region (Mammalian Phenotype Ontology, MP_0008581)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008581
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Genes

6 gene mutations causing the disorganized photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARL6 ADP-ribosylation factor-like 6
BBS1 Bardet-Biedl syndrome 1
CLCN2 chloride channel, voltage-sensitive 2
OAT ornithine aminotransferase
RHO rhodopsin
RP1 retinitis pigmentosa 1 (autosomal dominant)