Skor2 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Skor2
SKI family transcriptional corepressor 2
MGI:3645984

12 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Skor2^{Tn(sb-Tyr)1799B.CA3Ove}/Skor2^{Tn(sb-Tyr)1799B.CA3Ove} involves: FVB/N	abnormal gait	J:178818
	abnormal neuromuscular synapse morphology	J:178818
	decreased body size	J:178818
	prenatal lethality, incomplete penetrance	J:178818
	respiratory failure	J:178818
Skor2^{Tn(sb-Tyr)1799B.CA7BOve}/Skor2^{Tn(sb-Tyr)1799B.CA7BOve} involves: FVB/N	abnormal cerebellum development	J:178891
	abnormal cerebellum morphology	J:178891
	abnormal food intake	J:178891
	abnormal gait	J:178891
	abnormal Purkinje cell differentiation	J:178891
	ataxia	J:178891
	cleft secondary palate	J:178891
	decreased body size	J:178891
	decreased cerebellar granule cell precursor proliferation	J:178891
	prenatal lethality, incomplete penetrance	J:178891
	respiratory failure	J:178891

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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