About   Help   FAQ
Phenotypic Alleles
Query Results -- Summary
 Symbol
Name
ID
Mpv17
MpV17 mitochondrial inner membrane protein
MGI:97138

1 matching Allele (1 Gene/Marker represented)
                                        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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
04/08/2014
MGI 5.17
The Jackson Laboratory