abnormal intraocular pressure Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly in the amount of force per unit area exerted by the intraocular fluid within the eye. (Human Phenotype Ontology, HP_0012632)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005257
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15 gene mutations causing the abnormal intraocular pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADORA3 adenosine A3 receptor
BEST2 bestrophin 2
BMP4 bone morphogenetic protein 4
COL1A1 collagen, type I, alpha 1
GUCY1A3 guanylate cyclase 1, soluble, alpha 3
LEPR leptin receptor
LMX1B LIM homeobox transcription factor 1, beta
MYOC myocilin, trabecular meshwork inducible glucocorticoid response
PRSS56 protease, serine, 56
ROCK1 Rho-associated, coiled-coil containing protein kinase 1
ROCK2 Rho-associated, coiled-coil containing protein kinase 2
SH3PXD2B SH3 and PX domains 2B
TDRD7 tudor domain containing 7
TYR tyrosinase
VAV2 vav 2 guanine nucleotide exchange factor