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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Ckmt1tm2Bew/Ckmt1tm2Bew
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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last database update
02/11/2020
MGI 6.14
The Jackson Laboratory