Slc25a19 Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/12/2024 MGI 6.24