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Symbol
Name
ID

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

Phenotype annotations related to limbs/digits/tail

Darker colors indicate more annotations

Human Phenotypes	Pes cavus	Congenital hip dislocation	Distal lower limb muscle weakness	Limb-girdle muscle weakness
Disease(s) Associated with SLC25A1
congenital myasthenic syndrome

Mouse Phenotypes		abnormal limb morphology	abnormal tail morphology
Availability	Mouse Genotype	abnormal limb morphology	abnormal tail morphology
	Slc25a1^{em1(IMPC)Kmpc}/Slc25a1^{em1(IMPC)Kmpc}
	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)
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