Spart Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Spart
spartin
MGI:2139806

26 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Spart^tm1.1Xen/Spart^tm1.1Xen involves: C57BL/6J	abnormal adipose tissue morphology	J:185987
	abnormal axon morphology	J:185987
	abnormal cell migration	J:185987
	abnormal cell morphology	J:185987
	abnormal chondrocyte morphology	J:185987
	abnormal dendrite morphology	J:185987
	abnormal fat cell morphology	J:185987
	abnormal gait	J:185987
	abnormal mitosis	J:185987
	abnormal motor capabilities/coordination/movement	J:185987
	decreased circulating triglyceride level	J:185987
	decreased fat cell size	J:185987
	impaired coordination	J:185987
	increased blood uric acid level	J:185987
	increased cell nucleus count	J:185987
	increased total body fat amount	J:185987
	increased tumor incidence	J:185987
	limb grasping	J:185987
	normal nervous system phenotype	J:185987
	paraparesis	J:185987
	paresis	J:185987
	normal skeleton phenotype	J:185987
Spart^{tm2b(EUCOMM)Hmgu}/Spart^{tm2b(EUCOMM)Hmgu} C57BL/6N-Spart^{tm2b(EUCOMM)Hmgu}/Cnrm	decreased exploration in new environment	J:211773
	dilated aorta	J:211773
	increased fasting circulating glucose level	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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