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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Calb2
calbindin 2
MGI:101914
6 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Calb2tm1(cre)Zjh/Calb2tm1(cre)Zjh
involves: C57BL/6
no abnormal phenotype detected J:151755
Calb2tm1Map/Calb2tm1Map
involves: 129P2/OlaHsd * C57BL/6JIco
abnormal long-term potentiation J:42924
abnormal nervous system electrophysiology J:54517
normal behavior/neurological phenotype J:42924
impaired coordination J:54517
Calb2tm2.1(cre/ERT2)Zjh/Calb2+
involves: C57BL/6 * SJL
no abnormal phenotype detected J:151755
Calb2tm2.1(cre/ERT2)Zjh/Calb2tm2.1(cre/ERT2)Zjh
involves: C57BL/6 * SJL
abnormal nervous system electrophysiology J:151755
impaired coordination J:151755
reduced long-term potentiation J:151755

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
04/30/2024
MGI 6.23
The Jackson Laboratory