abnormal mitochondrial chromosome morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structrual anomaly of the chromosome found in the mitochondrion of a eukaryotic cell (Mammalian Phenotype Ontology, MP_0011638)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011638
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14 gene mutations causing the abnormal mitochondrial chromosome morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BDKRB2 bradykinin receptor B2
CLPP caseinolytic mitochondrial matrix peptidase proteolytic subunit
CTF1 cardiotrophin 1
MPV17 MpV17 mitochondrial inner membrane protein
MTERF2 mitochondrial transcription termination factor 2
OMA1 OMA1 zinc metallopeptidase
PDSS2 prenyl (decaprenyl) diphosphate synthase, subunit 2
POLG2 polymerase (DNA directed), gamma 2, accessory subunit
PRKG1 protein kinase, cGMP-dependent, type I
RNASEH1 ribonuclease H1
SESN2 sestrin 2
SUCLA2 succinate-CoA ligase, ADP-forming, beta subunit
TFAM transcription factor A, mitochondrial
TK2 thymidine kinase 2, mitochondrial