Mmaa Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mmaa
methylmalonic aciduria (cobalamin deficiency) type A
MGI:1923805

23 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Mmaa^em1(IMPC)J/Mmaa^em1(IMPC)J C57BL/6NJ-Mmaa^em1(IMPC)J/Mmjax	abnormal bone structure	J:211773
	decreased body length	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	decreased circulating calcium level	J:211773
	decreased circulating total protein level	J:211773
	decreased erythrocyte cell number	J:211773
	decreased exploration in new environment	J:211773
	decreased heart rate	J:211773
	decreased lean body mass	J:211773
	decreased locomotor activity	J:211773
	decreased mean corpuscular hemoglobin concentration	J:211773
	decreased thigmotaxis	J:211773
	female infertility	J:211773
	increased circulating alanine transaminase level	J:211773
	increased circulating alkaline phosphatase level	J:211773
	increased circulating bilirubin level	J:211773
	increased grip strength	J:211773
	increased mean corpuscular hemoglobin	J:211773
	increased mean corpuscular volume	J:211773
	increased total body fat amount	J:211773
	prolonged RR interval	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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