Retinitis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0035333
Similar Terms
Downloads & Tools

Genes

20 genes associated with the disease Retinitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
C2CD3 C2 calcium-dependent domain containing 3
CASP8 caspase 8, apoptosis-related cysteine peptidase
CFLAR CASP8 and FADD-like apoptosis regulator
CISH cytokine inducible SH2-containing protein
CRH corticotropin releasing hormone
CXCL12 chemokine (C-X-C motif) ligand 12
DPYSL5 dihydropyrimidinase-like 5
FAS Fas cell surface death receptor
IFNL3 interferon, lambda 3
IL6 interleukin 6
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
NDP Norrie disease (pseudoglioma)
PLXNA2 plexin A2
PRKCG protein kinase C, gamma
PRPF31 pre-mRNA processing factor 31
RHO rhodopsin
RLBP1 retinaldehyde binding protein 1
SLC9A6 solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
SOCS1 suppressor of cytokine signaling 1
SOCS3 suppressor of cytokine signaling 3