Slc20a2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc20a2
solute carrier family 20, member 2
MGI:97851

44 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc20a2^{tm1a(EUCOMM)Wtsi}/Slc20a2⁺ C57BL/6N-Slc20a2^{tm1a(EUCOMM)Wtsi}/Wtsi	increased grip strength	J:211773
Slc20a2^{tm1a(EUCOMM)Wtsi}/Slc20a2^{tm1a(EUCOMM)Wtsi} C57BL/6N-Slc20a2^{tm1a(EUCOMM)Wtsi}/Wtsi	abnormal atrioventricular cushion morphology	J:239583
	abnormal auditory brainstem response	J:211773
	abnormal forebrain morphology	J:239583
	abnormal hypoglossal nerve topology	J:239583
	abnormal incisor color	J:211773
	abnormal iris morphology	J:211773
	abnormal lens morphology	J:211773
	abnormal liver vasculature morphology	J:239583
	abnormal spine curvature	J:211773
	abnormal vena cava morphology	J:239583
	absent pinna reflex	J:211773
	anomalous pulmonary venous connection	J:239583
	arteriovenous malformation	J:239583
	cataract	J:211773
	decreased body length	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	ectopic cartilage	J:239583
	embryo cyst	J:239583
	embryo tumor	J:239583
	eyelids fail to open	J:211773
	fusion of vertebral arches	J:239583
	increased circulating alkaline phosphatase level	J:211773
	increased circulating magnesium level	J:211773
	increased hemangioma incidence	J:239583
	irregularly shaped pupil	J:211773
	kyphosis	J:211773
	multiple persisting craniopharyngeal ducts	J:239583
	narrow eye opening	J:211773
	small superior cervical ganglion	J:239583
	subcutaneous edema	J:239583
Slc20a2^{tm1a(EUCOMM)Wtsi}/Slc20a2^{tm1a(EUCOMM)Wtsi} C57BL/6NTac-Slc20a2^{tm1a(EUCOMM)Wtsi}/Ieg	abnormal basal ganglion morphology	J:223197
	abnormal cerebral cortex morphology	J:223197
	abnormal mineral level	J:234034
	abnormal thalamus morphology	J:223197
	calcified brain	J:223197
	decreased circulating phosphate level	J:234034
	microgliosis	J:223197
Slc20a2^{tm1b(EUCOMM)Wtsi}/Slc20a2⁺ C57BL/6N-Slc20a2^{tm1b(EUCOMM)Wtsi}/Ieg	abnormal motor coordination/balance	J:211773
	abnormal vocalization	J:211773
	impaired glucose tolerance	J:211773
	increased total body fat amount	J:211773
Slc20a2^{tm1b(EUCOMM)Wtsi}/Slc20a2^{tm1b(EUCOMM)Wtsi} C57BL/6N-Slc20a2^{tm1b(EUCOMM)Wtsi}/Ieg	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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