absent photoreceptor inner segment Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence 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_0008583)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008583
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Genes

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

Symbol Name
ARL6 ADP-ribosylation factor-like 6
CLCN7 chloride channel, voltage-sensitive 7
CRX cone-rod homeobox
TULP1 tubby like protein 1