Optic Atrophy Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Xref MGI. (Human Disease Ontology, DOID_5723)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D009896
Similar Terms
Downloads & Tools

Genes

13 genes/proteins associated with the disease Optic Atrophy from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
NMNAT1 nicotinamide nucleotide adenylyltransferase 1 2.88009
NDUFS3 NADH dehydrogenase (ubiquinone) Fe-S protein 3, 30kDa (NADH-coenzyme Q reductase) 2.88009
DNM1L dynamin 1-like 2.88009
GSTP1 glutathione S-transferase pi 1 1.32221
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.31237
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1) 1.20361
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.16633
F2 coagulation factor II (thrombin) 1.15458
CAT catalase 1.13895
BCL2 B-cell CLL/lymphoma 2 1.08797
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.06698
MYC v-myc avian myelocytomatosis viral oncogene homolog 1.0561
IL6 interleukin 6 1.04014