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Symbol
Name
ID

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

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes	Weakness of facial musculature	Tongue fasciculations
Disease(s) Associated with SLC25A21	Weakness of facial musculature	Tongue fasciculations
mitochondrial DNA depletion syndrome 18

Mouse Phenotypes		abnormal cranium morphology	abnormal tooth morphology	abnormal incisor morphology	abnormal mandible morphology	abnormal snout morphology
Availability	Mouse Genotype
	Slc25a21^{tm1a(KOMP)Wtsi}/Slc25a21^{tm1a(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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23