abnormal mitochondrial proliferation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the expansion rate of the cellular organelles responsible for energy production by division (Mammalian Phenotype Ontology, MP_0006037)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006037
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4 gene mutations causing the abnormal mitochondrial proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
LBR lamin B receptor
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
UCP2 uncoupling protein 2 (mitochondrial, proton carrier)
VCP valosin containing protein