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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Mmut
methylmalonyl-Coenzyme A mutase
MGI:97239
52 phenotypes from 5 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Mmutem1Cpv/Mmutem1Cpv
involves: 129S/SvEv * C57BL/6 * FVB/N 		decreased body weight J:332892
increased circulating methylmalonic acid level J:332892
postnatal growth retardation J:332892
postnatal lethality, incomplete penetrance J:332892
premature death J:332892
Mmutem2Cpv/Mmutem2Cpv
involves: 129S/SvEv * C57BL/6 * FVB/N 		increased circulating methylmalonic acid level J:332892
normal mortality/aging J:332892
postnatal growth retardation J:332892
Mmuttm1.1Mrb/Mmuttm1.1Mrb
involves: C57BL/6 		abnormal fatty acids level J:237040
acidosis J:237040
increased circulating ammonia level J:237040
increased circulating carnitine level J:237040
increased circulating glycine level J:237040
methylmalonic aciduria J:237040
normal mortality/aging J:237040
postnatal growth retardation J:237040
weight loss J:237040
Mmuttm1Cpv/Mmuttm1Cpv
involves: 129S/SvEv * C57BL/6 		neonatal lethality, incomplete penetrance J:147313
Mmuttm1Cpv/Mmuttm1Cpv
involves: 129S/SvEv * C57BL/6 * FVB/N 		abnormal blood homeostasis J:147313
abnormal circulating amino acid level J:147313
abnormal exocrine pancreas morphology J:147313
abnormal hepatocyte mitochondrial morphology J:147313
abnormal pancreas morphology J:147313
abnormal pancreatic beta cell morphology J:147313
abnormal proximal convoluted tubule morphology J:147313
abnormal respiratory electron transport chain J:147313
abnormal tricarboxylic acid cycle J:147313
decreased body weight J:147313
decreased survivor rate J:147313
hepatic steatosis J:147313
organic aciduria J:147313
postnatal growth retardation J:147313
postnatal lethality, incomplete penetrance J:147313
tubulointerstitial nephritis J:147313
Mmuttm1Cpv/Mmuttm1Cpv
Not Specified 		abnormal blood homeostasis J:147338
abnormal brain morphology J:147338
abnormal liver morphology J:147338
acidemia J:147338
aciduria J:147338
dehydration J:147338
lung hemorrhage J:147338
postnatal lethality, complete penetrance J:147338
respiratory distress J:147338
Mmuttm1Pai/Mmuttm1.1Mrb
involves: 129S1/Sv * C57BL/6 		abnormal brain morphology J:237040
abnormal fatty acids level J:237040
abnormal kidney morphology J:237040
abnormal kidney physiology J:237040
abnormal sphingolipid level J:237040
acidosis J:237040
decreased body weight J:237040
increased blood urea nitrogen level J:237040
increased brain weight J:237040
increased circulating ammonia level J:237040
increased circulating carnitine level J:237040
increased circulating glycine level J:237040
increased lipocalin 2 level J:237040
increased urine calcium level J:237040
increased urine chloride ion level J:237040
increased urine magnesium level J:237040
increased urine potassium level J:237040
increased urine sodium level J:237040
methylmalonic aciduria J:237040
normal mortality/aging J:237040
oliguria J:237040
postnatal growth retardation J:237040
weight loss J:237040
Mmuttm1Pai/Mmuttm1Pai
involves: 129S1/Sv * C57BL/6 		abnormal liver parenchyma morphology J:87081
abnormal suckling behavior J:87081
absent gastric milk in neonates J:87081
decreased locomotor activity J:87081
increased circulating carnitine level J:87081
methylmalonic aciduria J:87081
neonatal lethality, complete penetrance J:87081
respiratory distress J:87081
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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Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory