ruptured lens capsule Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a break or tear in the elastic, clear, membrane-like structure, that is outer most layer of the lens (Mammalian Phenotype Ontology, MP_0008841)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008841
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Genes

12 gene mutations causing the ruptured lens capsule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BCAR3 breast cancer anti-estrogen resistance 3
CRYAA crystallin, alpha A
CRYGA crystallin, gamma A
GJA8 gap junction protein, alpha 8, 50kDa
HSF4 heat shock transcription factor 4
LIM2 lens intrinsic membrane protein 2, 19kDa
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
PXDN peroxidasin
SPARC secreted protein, acidic, cysteine-rich (osteonectin)
TBC1D20 TBC1 domain family, member 20
TDRD7 tudor domain containing 7
TGFA transforming growth factor, alpha