Ckmt1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ckmt1
creatine kinase, mitochondrial 1, ubiquitous
MGI:99441

13 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Ckmt1^tm2Bew/Ckmt1^tm2Bew involves: 129P2/OlaHsd * C57BL/6	abnormal hearing physiology	J:116302
	abnormal prepulse inhibition	J:116302
	abnormal spatial learning	J:116302
	normal behavior/neurological phenotype	J:116302
	decreased exploration in new environment	J:116302
	decreased grooming behavior	J:116302
	decreased startle reflex	J:116302
	decreased vertical activity	J:116302
	normal growth/size/body region phenotype	J:116302
	normal homeostasis/metabolism phenotype	J:116302
	increased defecation amount	J:116302
	normal integument phenotype	J:116302
	normal reproductive system phenotype	J:27221, J:116302

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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