abnormal mitochondrial matrix morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the gel-like material, with considerable fine structure, that lies in the matrix space, or lumen, of a mitochondrion, and contains the enzymes of the tricarboxylic acid cycle and, in some organisms, the enzymes concerned with fatty acid oxidation (Mammalian Phenotype Ontology, MP_0011637)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011637
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1 gene mutations causing the abnormal mitochondrial matrix morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1