retinal atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001105
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Genes

8 genes associated with the retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CTSD cathepsin D
LAMA1 laminin, alpha 1
MERTK MER proto-oncogene, tyrosine kinase
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
POMT1 protein-O-mannosyltransferase 1
RBP4 retinol binding protein 4, plasma
RS1 retinoschisin 1
SLC7A14 solute carrier family 7, member 14