Optic Atrophy Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Xref MGI. (Human Disease Ontology, DOID_5723)
Similar Terms
Downloads & Tools

Genes

15 genes associated with the Optic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ARMS2 age-related maculopathy susceptibility 2
C2 complement component 2
C3 complement component 3
CFB complement factor B
CFH complement factor H
CISD2 CDGSH iron sulfur domain 2
HTRA1 HtrA serine peptidase 1
LIPC lipase, hepatic
MT-ATP6 ATP synthase F0 subunit 6
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
ND1
OPA1 optic atrophy 1 (autosomal dominant)
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
WFS1 Wolfram syndrome 1 (wolframin)