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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Mpv17
MpV17 mitochondrial inner membrane protein
MGI:97138
74 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Mpv17/Mpv17
CFW-Mpv17/J
abnormal auditory brainstem response J:48661
abnormal blood homeostasis J:10661
abnormal coat/hair pigmentation J:143355
abnormal cochlea morphology J:48653
abnormal glomerular capillary morphology J:10661
abnormal hepatocyte morphology J:143355
abnormal hypodermis muscle layer morphology J:143355
abnormal liver lobule morphology J:143355
abnormal liver sinusoid morphology J:143355
abnormal mitochondrial crista morphology J:143355
abnormal portal triad morphology J:143355
abnormal renal glomerulus morphology J:108252, J:143355
abnormal renal tubule morphology J:108252
abnormal renal/urinary system physiology J:59102
abnormal scala media morphology J:48653
abnormal sebaceous gland morphology J:143355
abnormal skin morphology J:143355
albuminuria J:62419, J:108252
anemia J:10661
cachexia J:10661
normal cellular phenotype J:143355
cochlear ganglion degeneration J:48662
cochlear ganglion hypoplasia J:48653
cochlear outer hair cell degeneration J:48662
cortical renal glomerulopathies J:10661, J:108252
decreased body weight J:143355
decreased circulating serum albumin level J:10661, J:62419
decreased erythrocyte cell number J:10661
decreased hair follicle number J:143355
decreased hemoglobin content J:10661
decreased hepatocyte mitochondrial DNA content J:143355
decreased locomotor activity J:10661
decreased mitochondrial DNA content J:143355
decreased muscle fiber mitochondrial DNA content J:143355
decreased subcutaneous adipose tissue amount J:143355
decreased urine osmolality J:59102
dilated mitochondrion J:143355
dilated renal tubule J:10661
expanded mesangial matrix J:108252
fused podocyte foot processes J:10661
glomerulosclerosis J:10661, J:143355
normal homeostasis/metabolism phenotype J:143355
hypertension J:59102
increased blood urea nitrogen level J:10661
increased circulating alanine transaminase level J:143355
increased circulating aspartate transaminase level J:143355
increased circulating cholesterol level J:10661
increased circulating creatine kinase level J:143355
increased circulating creatinine level J:10661
increased circulating lactate level J:143355
increased heart rate J:59102
increased kidney weight J:62419
increased or absent threshold for auditory brainstem response J:48661
increased urine protein level J:10661, J:108252, J:143355
increased urine sodium level J:59102
kidney degeneration J:143355
kidney failure J:48662
normal liver/biliary system phenotype J:143355
organ of Corti degeneration J:48653, J:48662
podocyte foot process effacement J:108252
polyuria J:59102
premature death J:10661, J:27358, J:62419, J:143355
renal glomerulus hypertrophy J:10661, J:108252
renal interstitial fibrosis J:143355
sensorineural hearing loss J:48661, J:48662
small sebaceous gland J:143355
spiral ligament degeneration J:48653, J:48662
stria vascularis degeneration J:48653, J:48662
thin epidermis J:143355
thin skin J:143355
Mpv17em1(IMPC)J/Mpv17em1(IMPC)J
C57BL/6NJ-Mpv17em1(IMPC)J/J
decreased circulating glucose level J:211773
decreased mean corpuscular hemoglobin J:211773
increased blood urea nitrogen level J:211773
increased heart weight J:211773
thrombocytopenia J:211773

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory