Slc25a20 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc25a20
solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20
MGI:1928738

16 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc25a20^{tm1a(EUCOMM)Wtsi}/Slc25a20^{tm1a(EUCOMM)Wtsi} C57BL/6N-Slc25a20^{tm1a(EUCOMM)Wtsi}/Wtsi	abnormal dorsal pancreas topology	J:239583
	abnormal Mullerian duct morphology	J:239583
	abnormal vitelline vein topology	J:239583
	abnormal Wolffian duct topology	J:239583
	cerebral arteriovenous malformation	J:239583
	double ureter	J:239583
	ductus venosus stenosis	J:239583
	edema	J:239583
	embryo cyst	J:239583
	herniated liver	J:239583
	jugular vein stenosis	J:239583
	multiple persisting craniopharyngeal ducts	J:239583
	placenta hemorrhage	J:261316
	preweaning lethality, complete penetrance	J:211773, J:261316
	retropleural edema	J:239583
	umbilical vein stenosis	J:239583

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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