nuclear cataracts Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a lens opacity located in the dense, central part of the lens (Mammalian Phenotype Ontology, MP_0010254)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010254
Similar Terms
Downloads & Tools

Genes

16 gene mutations causing the nuclear cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CRYAA crystallin, alpha A
CRYBB2 crystallin, beta B2
CRYGA crystallin, gamma A
CRYGB crystallin, gamma B
CRYGC crystallin, gamma C
CRYGD crystallin, gamma D
DMD dystrophin
GGT1 gamma-glutamyltransferase 1
GJA8 gap junction protein, alpha 8, 50kDa
HIP1 huntingtin interacting protein 1
LIM2 lens intrinsic membrane protein 2, 19kDa
MAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
NRCAM neuronal cell adhesion molecule
SEP15 15 kDa selenoprotein
SIX5 SIX homeobox 5
SREBF2 sterol regulatory element binding transcription factor 2