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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Chp1
calcineurin-like EF hand protein 1
MGI:1927185
14 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Chp1em1(IMPC)Tcp/Chp1+
C57BL/6NCrl-Chp1em1(IMPC)Tcp/Tcp
abnormal coat/ hair morphology J:211773
abnormal embryo size J:211773
decreased mean corpuscular hemoglobin J:211773
decreased mean corpuscular volume J:211773
embryonic growth retardation J:211773
Chp1em1(IMPC)Tcp/Chp1em1(IMPC)Tcp
C57BL/6NCrl-Chp1em1(IMPC)Tcp/Tcp
abnormal embryo size J:211773
embryonic growth retardation J:211773
embryonic lethality prior to tooth bud stage J:211773
preweaning lethality, complete penetrance J:211773
Chp1vac/Chp1vac
B6(C3Fe)-Chp1vac
abnormal Purkinje cell axon morphology J:199873
abnormal synaptic bouton morphology J:199873
ataxia J:199873
axon degeneration J:199873
axonal dystrophy J:199873
Purkinje cell degeneration J:199873
tremors J:199873

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
11/19/2024
MGI 6.24
The Jackson Laboratory