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Symbol
Name
ID

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

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Scoliosis
Disease(s) Associated with SLC25A21	Scoliosis
mitochondrial DNA depletion syndrome 18

Mouse Phenotypes		abnormal cranium morphology	abnormal tooth morphology	abnormal incisor morphology	abnormal mandible morphology	decreased bone mineral content	abnormal joint morphology
Availability	Mouse Genotype	abnormal cranium morphology	abnormal tooth morphology	abnormal incisor morphology	abnormal mandible morphology	decreased bone mineral content	abnormal joint morphology
	Slc25a21^{tm1a(KOMP)Wtsi}/Slc25a21^{tm1a(KOMP)Wtsi}
	Slc25a21^{tm1d(KOMP)Wtsi}/Slc25a21^{tm1d(KOMP)Wtsi}

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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