abnormal eye anterior chamber morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the space in the eye, filled with aqueous humor, and bounded anteriorly by the cornea and a small portion of the sclera and posteriorly by a small portion of the ciliary body, the iris, and part of the crystalline lens (Mammalian Phenotype Ontology, MP_0005205)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005205
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26 gene mutations causing the abnormal eye anterior chamber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BCAR3 breast cancer anti-estrogen resistance 3
COL4A2 collagen, type IV, alpha 2
COL8A1 collagen, type VIII, alpha 1
COL8A2 collagen, type VIII, alpha 2
EGR1 early growth response 1
FGF9 fibroblast growth factor 9
FOXC1 forkhead box C1
FOXE3 forkhead box E3
GNPAT glyceronephosphate O-acyltransferase
GUCY1A3 guanylate cyclase 1, soluble, alpha 3
LIMK2 LIM domain kinase 2
LMX1B LIM homeobox transcription factor 1, beta
LYST lysosomal trafficking regulator
MCPH1 microcephalin 1
OTX1 orthodenticle homeobox 1
PAX6 paired box 6
PITX2 paired-like homeodomain 2
PRSS56 protease, serine, 56
PVRL3 poliovirus receptor-related 3
PXDN peroxidasin
ROCK2 Rho-associated, coiled-coil containing protein kinase 2
RUFY2 RUN and FYVE domain containing 2
SH3PXD2B SH3 and PX domains 2B
TDRD7 tudor domain containing 7
TGFA transforming growth factor, alpha
TGFB2 transforming growth factor, beta 2