dilated mitochondria Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the luminal space of the mitochondria is increased in volume or area, usually with an increase of contained fluid (Mammalian Phenotype Ontology, MP_0011632)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011632
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Genes

5 gene mutations causing the dilated mitochondria phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHDH choline dehydrogenase
CTNS cystinosin, lysosomal cystine transporter
MPV17 MpV17 mitochondrial inner membrane protein
MUC2 mucin 2, oligomeric mucus/gel-forming
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1