retinal detachment Gene Set

Dataset MPO 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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11 gene mutations causing the retinal detachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BEST1 bestrophin 1
BMP4 bone morphogenetic protein 4
CDKN2A cyclin-dependent kinase inhibitor 2A
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1
LDLR low density lipoprotein receptor
MITF microphthalmia-associated transcription factor
PDGFRB platelet-derived growth factor receptor, beta polypeptide
RHO rhodopsin
RPL24 ribosomal protein L24
SPARC secreted protein, acidic, cysteine-rich (osteonectin)
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box)