Camkmt Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Camkmt
calmodulin-lysine N-methyltransferase
MGI:1920832

17 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Camkmt^{tm1b(EUCOMM)Wtsi}/Camkmt^{tm1b(EUCOMM)Wtsi} C57BL/6N-Camkmt^{tm1b(EUCOMM)Wtsi}/Wtsi	decreased total body fat amount	J:211773
	increased blood urea nitrogen level	J:211773
	increased circulating creatinine level	J:211773
	increased circulating sodium level	J:211773
	increased mean platelet volume	J:211773
Camkmt^tm1Rpav/Camkmt^tm1Rpav B6.129S7-Camkmt^tm1Rpav	abnormal behavior	J:228818
	normal behavior/neurological phenotype	J:228818
	behavioral developmental delay	J:228818
	decreased body weight	J:228818
	decreased grip strength	J:228818
	impaired coordination	J:228818
	impaired passive avoidance behavior	J:228818
	normal muscle phenotype	J:228818
Camkmt^tm1Rpav/Camkmt^tm1Rpav involves: 129S7/SvEvBrd * C57BL/6J	abnormal mitochondrial ATP synthesis coupled electron transport	J:228818
	increased variability of skeletal muscle fiber size	J:228818
	myopathy	J:228818
	normal renal/urinary system phenotype	J:228818

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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