abnormal mitochondrial shape Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly in the surface contour of mitochondria. (Human Phenotype Ontology, HP_0012087)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011633
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7 gene mutations causing the abnormal mitochondrial shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRG6 adhesion G protein-coupled receptor G6
CISD2 CDGSH iron sulfur domain 2
COL6A3 collagen, type VI, alpha 3
NDUFA13 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1
THEM5 thioesterase superfamily member 5
TLR2 toll-like receptor 2