Slc25a19 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc25a19
solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
MGI:1914533

15 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc25a19^tm1Mjl/Slc25a19^tm1Mjl either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	abnormal amniotic fluid composition	J:115337
	abnormal enzyme/coenzyme activity	J:115337
	abnormal mitochondrial physiology	J:115337
	absent brain ventricles	J:115337
	anemia	J:115337
	decreased embryo size	J:115337
	embryo tissue necrosis	J:115337
	embryonic growth arrest	J:115337
	embryonic lethality during organogenesis, complete penetrance	J:115337
	exencephaly	J:115337
	ketoaciduria	J:115337
	microcephaly	J:115337
	open neural tube	J:115337
	pale yolk sac	J:115337
	wavy neural tube	J:115337

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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