abnormal retinal blood vessel morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the blood vessels supplying the retina (Mammalian Phenotype Ontology, MP_0010097)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010097
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14 gene mutations causing the abnormal retinal blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANGPTL4 angiopoietin-like 4
CBS cystathionine-beta-synthase
CRX cone-rod homeobox
DOT1L DOT1-like histone H3K79 methyltransferase
FGF10 fibroblast growth factor 10
LAMA1 laminin, alpha 1
NOS1AP nitric oxide synthase 1 (neuronal) adaptor protein
NPHP4 nephronophthisis 4
NRP1 neuropilin 1
PAX2 paired box 2
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
PROM1 prominin 1
ROM1 retinal outer segment membrane protein 1
SIRT1 sirtuin 1