Slc25a28 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc25a28
solute carrier family 25, member 28
MGI:2180509

8 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc25a28^tm1.1Dwrd/Slc25a28^tm1.1Dwrd Speer6-ps1^{Tg(Alb-cre)21Mgn}/0 involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCrl * DBA	abnormal oxidative phosphorylation	J:300667
	decreased liver iron level	J:300667
	normal embryo phenotype	J:300667
Slc25a28^tm1.2Dwrd/Slc25a28^tm1.2Dwrd involves: 129S6/SvEvTac * C57BL/6NCrl	abnormal oxidative phosphorylation	J:300667
	asthenozoospermia	J:300667
	decreased liver iron level	J:300667
	normal hematopoietic system phenotype	J:300667
	oligozoospermia	J:300667
	reduced male fertility	J:300667
Slc25a28^{tm1b(EUCOMM)Wtsi}/Slc25a28^{tm1b(EUCOMM)Wtsi} C57BL/6N-Slc25a28^{tm1b(EUCOMM)Wtsi}/Wtsi	abnormal cornea morphology	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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