Symbol Name ID

Mpv17 MpV17 mitochondrial inner membrane protein MGI:97138

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1 matching Allele (1 Gene/Marker represented)

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                                        Allele Symbol
Name                                           Chr  Synonyms                Category                                                                                                                             Phenotypic Classes                                                                                                                                                                                        Human Diseases                                                                          

Mpv17
MpV17 mitochondrial inner membrane protein; Mpv17 retroviral insertion, kidney disease mutant  5    MPV-      Transgenic (random, gene disruption)  adipose, behavior, cardiovascular, cellular, endocrine/exocrine, growth/size, hearing/vestibular/ear, hematopoietic, homeostasis, integument, liver/biliary, mortality/aging, muscle, nervous system, pigmentation, renal/urinary, skeleton  Alport Syndrome, Autosomal Recessive 203780; Mitochondrial DNA Depletion Syndrome 3 (hepatocerebral Type); MTDPS3 251880; Nephrotic Syndrome, Type 2; NPHS2 600995