Retinal Detachment Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_5327)
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22 genes associated with the Retinal Detachment phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ARMS2 age-related maculopathy susceptibility 2
CERS2 ceramide synthase 2
CFH complement factor H
COL2A1 collagen, type II, alpha 1
IFNG interferon, gamma
IL6 interleukin 6
LDB2 LIM domain binding 2
LOX lysyl oxidase
LST1 leukocyte specific transcript 1
LTA lymphotoxin alpha
NCR3 natural cytotoxicity triggering receptor 3
PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SMAD7 SMAD family member 7
SS18 synovial sarcoma translocation, chromosome 18
TGFB1 transforming growth factor, beta 1
TIAM1 T-cell lymphoma invasion and metastasis 1
TNF tumor necrosis factor
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B
TP53 tumor protein p53
TSTA3 tissue specific transplantation antigen P35B
WRN Werner syndrome, RecQ helicase-like