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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cc2d1a
coiled-coil and C2 domain containing 1A
MGI:2384831
16 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cc2d1atm1a(KOMP)Wtsi/Cc2d1atm1a(KOMP)Wtsi
involves: C57BL/6J * C57BL/6N
decreased interferon-beta secretion J:190401
decreased interleukin-6 secretion J:190401
Cc2d1atm1Bisu/Cc2d1atm1Bisu
Not Specified
abnormal brain vasculature morphology J:184920
abnormal dendrite morphology J:184920
abnormal neuron physiology J:184920
decreased body weight J:184920
decreased CNS synapse formation J:184920
hunched posture J:184920
increased cellular sensitivity to hydrogen peroxide J:184920
neonatal lethality, incomplete penetrance J:184920
respiratory distress J:184920
Cc2d1atm1Zjc/Cc2d1atm1Zjc
involves: 129S/SvEv * C57BL/6
abnormal excitatory postsynaptic currents J:177407
abnormal inhibitory postsynaptic currents J:177407
abnormal miniature inhibitory postsynaptic currents J:177407
abnormal synaptic vesicle recycling J:177407
perinatal lethality, complete penetrance J:177407

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
07/07/2020
MGI 6.15
The Jackson Laboratory