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Symbol
Name
ID

Slc25a1
solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1
MGI:1345283

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Esotropia	Nystagmus	Ophthalmoplegia	Diplopia	Cerebral visual impairment	Ptosis	Staring gaze
Disease(s) Associated with SLC25A1	Esotropia	Nystagmus	Ophthalmoplegia	Diplopia	Cerebral visual impairment	Ptosis	Staring gaze
combined D-2- and L-2-hydroxyglutaric aciduria
congenital myasthenic syndrome

Mouse Phenotypes		anophthalmia
Availability	Mouse Genotype	anophthalmia
	Slc25a1^{tm1b(EUCOMM)Wtsi}/Slc25a1^{tm1b(EUCOMM)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 04/16/2024 MGI 6.23