Cbln1 Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23