persistence of hyaloid vascular system Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure of the degeneration of the transient vascular system of the eye during development, that normally nourishes the retina, immature lens and primary vitreous of the developing eye (Mammalian Phenotype Ontology, MP_0001289)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001289
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Genes

26 gene mutations causing the persistence of hyaloid vascular system phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGAP1 ArfGAP with GTPase domain, ankyrin repeat and PH domain 1
ANGPT2 angiopoietin 2
APAF1 apoptotic peptidase activating factor 1
BMP4 bone morphogenetic protein 4
CDKN2A cyclin-dependent kinase inhibitor 2A
CHD7 chromodomain helicase DNA binding protein 7
CLSTN1 calsyntenin 1
COL18A1 collagen, type XVIII, alpha 1
FGF10 fibroblast growth factor 10
FZD4 frizzled class receptor 4
GNPAT glyceronephosphate O-acyltransferase
LAMA1 laminin, alpha 1
LEF1 lymphoid enhancer-binding factor 1
LRP5 low density lipoprotein receptor-related protein 5
MYO10 myosin X
MYO7A myosin VIIA
NR2E1 nuclear receptor subfamily 2, group E, member 1
PRKCZ protein kinase C, zeta
RARB retinoic acid receptor, beta
RPL24 ribosomal protein L24
SIRT1 sirtuin 1
SPI1 Spi-1 proto-oncogene
TGFB2 transforming growth factor, beta 2
TSPAN12 tetraspanin 12
VEGFA vascular endothelial growth factor A
WNT7B wingless-type MMTV integration site family, member 7B