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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cabp7
calcium binding protein 7
MGI:2183437
11 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cabp7tm1.1Yyam/Cabp7tm1.1Yyam
Tg(ACTA1-cre)79Jme/0
B6.Cg-Cabp7tm1.1Yyam Tg(ACTA1-cre)79Jme
abnormal action potential J:345130
abnormal muscle electrophysiology J:345130
abnormal neuromuscular synapse morphology J:345130
decreased grip strength J:345130
decreased skeletal muscle mass J:345130
impaired coordination J:345130
muscle weakness J:345130
muscular atrophy J:345130
neuromuscular synapse degeneration J:345130
premature death J:345130
Tg(Syn1-Cabp7/mCherry)1Mrkr/0
Not Specified
normal nervous system phenotype J:338143

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
04/07/2026
MGI 6.24
The Jackson Laboratory