small lens Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the transparent structure of the eye responsible for focusing light rays (Mammalian Phenotype Ontology, MP_0001306)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001306
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Genes

39 gene mutations causing the small lens phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
CRYAA crystallin, alpha A
CRYAB crystallin, alpha B
CRYBA2 crystallin, beta A2
CRYBB2 crystallin, beta B2
CRYGC crystallin, gamma C
CRYGD crystallin, gamma D
FGF9 fibroblast growth factor 9
FIGN fidgetin
FOXC1 forkhead box C1
FOXE3 forkhead box E3
GAS1 growth arrest-specific 1
GJA8 gap junction protein, alpha 8, 50kDa
GJE1 gap junction protein, epsilon 1, 23kDa
HIP1 huntingtin interacting protein 1
HSF4 heat shock transcription factor 4
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LIM2 lens intrinsic membrane protein 2, 19kDa
MAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
MEIS1 Meis homeobox 1
MIP major intrinsic protein of lens fiber
MSX2 msh homeobox 2
NCAPH non-SMC condensin I complex, subunit H
NCOA6 nuclear receptor coactivator 6
PAX6 paired box 6
PKNOX1 PBX/knotted 1 homeobox 1
POU2F1 POU class 2 homeobox 1
PVRL3 poliovirus receptor-related 3
PXDN peroxidasin
PYGO2 pygopus family PHD finger 2
RAX retina and anterior neural fold homeobox
RDH10 retinol dehydrogenase 10 (all-trans)
SOX1 SRY (sex determining region Y)-box 1
SPNS2 spinster homolog 2 (Drosophila)
TBC1D20 TBC1 domain family, member 20
TBC1D32 TBC1 domain family, member 32
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
VSX2 visual system homeobox 2