Limch1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Limch1
LIM and calponin homology domains 1
MGI:1924819

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Limch1^em1Coop/Limch1^em1Coop FVB-Limch1^em1Coop	abnormal calcium ion homeostasis	J:336773
	abnormal skeletal muscle fiber morphology	J:336773
	decreased grip strength	J:336773
	impaired muscle relaxation	J:336773
	impaired skeletal muscle contractility	J:336773
	normal muscle phenotype	J:336773
	muscle weakness	J:336773
Limch1^{tm1b(EUCOMM)Hmgu}/Limch1^{tm1b(EUCOMM)Hmgu} C57BL/6N-Limch1^{tm1b(EUCOMM)Hmgu}/J	abnormal retina morphology	J:211773
	abnormal sleep behavior	J:211773
	preweaning lethality, incomplete penetrance	J:211773

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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