Cbln1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cbln1
cerebellin 1 precursor protein
MGI:88281

10 phenotypes from 4 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cbln1^tm1.1Mmsh/Cbln1^tm1.1Mmsh Tg(Grin2c-cre/PGR)25Mim/0 involves: C57BL/6	abnormal synapse morphology	J:165995
Cbln1^tm1.2Mmsh/Cbln1^tm1.2Mmsh involves: C57BL/6	abnormal synapse morphology	J:165995
Cbln1^tm1Jim/Cbln1^tm1Jim involves: 129S7/SvEvBrd	abnormal cerebellar granule layer morphology	J:102516
	abnormal gait	J:102516
	abnormal long-term depression	J:102516
	abnormal Purkinje cell innervation	J:102516
	ataxia	J:102516
	decreased excitatory postsynaptic current amplitude	J:102516
	impaired coordination	J:102516
Cbln1^tm1Jim/Cbln1^tm1Jim Tg(Pcp2-Cbln1)#Jim/? involves: 129S7/SvEvBrd * FVB	normal behavior/neurological phenotype	J:182277
	normal nervous system phenotype	J:182277

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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