Oculomotor Nerve Paralysis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0028866
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Genes

22 genes associated with the disease Oculomotor Nerve Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACSM3 acyl-CoA synthetase medium-chain family member 3
AIP aryl hydrocarbon receptor interacting protein
ANGPTL6 angiopoietin-like 6
AQP4 aquaporin 4
CDC42 cell division cycle 42
CDH23 cadherin-related 23
CHN1 chimerin 1
COL25A1 collagen, type XXV, alpha 1
COL3A1 collagen, type III, alpha 1
ENG endoglin
KIF21A kinesin family member 21A
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
MEN1 multiple endocrine neoplasia I
NF2 neurofibromin 2 (merlin)
PDGFB platelet-derived growth factor beta polypeptide
PLEC plectin
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
SUFU suppressor of fused homolog (Drosophila)
TGFBR3 transforming growth factor, beta receptor III
TMEM8C transmembrane protein 8C
TRPV4 transient receptor potential cation channel, subfamily V, member 4
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1