Slc25a21 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc25a21
solute carrier family 25 (mitochondrial oxodicarboxylate carrier), member 21
MGI:2445059

20 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc25a21^{tm1a(KOMP)Wtsi}/Slc25a21^{tm1a(KOMP)Wtsi} B6JTyr;B6N-Slc25a21^{tm1a(KOMP)Wtsi}/Wtsi	abnormal cranium morphology	J:175295
	abnormal incisor morphology	J:175295
	abnormal joint morphology	J:175295
	abnormal mandible morphology	J:175295
	abnormal snout morphology	J:175295
	abnormal tooth morphology	J:175295
	absent pinna reflex	J:175295
	decreased body length	J:175295
	decreased body weight	J:175295
	decreased bone mineral content	J:175295
	decreased circulating alanine transaminase level	J:175295
	decreased circulating aspartate transaminase level	J:175295
	decreased circulating LDL cholesterol level	J:175295
	decreased circulating potassium level	J:175295
	decreased total body fat amount	J:175295
Slc25a21^{tm1d(KOMP)Wtsi}/Slc25a21^{tm1d(KOMP)Wtsi} B6Brd;B6Dnk;B6N-Tyr^c-Brd Slc25a21^{tm1a(KOMP)Wtsi}/Wtsi	decreased bone mineral content	J:211773
	decreased circulating magnesium level	J:211773
	decreased lean body mass	J:211773
	decreased mean corpuscular hemoglobin	J:211773
	decreased mean corpuscular volume	J:211773
	increased total body fat amount	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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