abnormal lens vesicle development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description malformation or abnormal patterning of the ectodermal invagination that forms opposite the optic cup in the primordium of the lens of the eye (Mammalian Phenotype Ontology, MP_0001292)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001292
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Genes

13 gene mutations causing the abnormal lens vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP7 bone morphogenetic protein 7
FOXE3 forkhead box E3
GJE1 gap junction protein, epsilon 1, 23kDa
GRIP1 glutamate receptor interacting protein 1
MAB21L1 mab-21-like 1 (C. elegans)
MAB21L2 mab-21-like 2 (C. elegans)
MAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
MSX2 msh homeobox 2
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
PAX6 paired box 6
RAB23 RAB23, member RAS oncogene family
SOX1 SRY (sex determining region Y)-box 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)