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Symbol
Name
ID

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

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Feeding difficulties	Nasal regurgitation	Poor suck	Choking episodes	Weak cry	Dysphonia	Hypernasal speech
Disease(s) Associated with SLC25A1	Decreased fetal movement	Feeding difficulties	Nasal regurgitation	Poor suck	Choking episodes	Weak cry	Dysphonia	Hypernasal speech
combined D-2- and L-2-hydroxyglutaric aciduria
congenital myasthenic syndrome

Mouse Phenotypes		increased exploration in new environment	no spontaneous movement
Availability	Mouse Genotype	increased exploration in new environment	no spontaneous movement
	Slc25a1^{em1(IMPC)Kmpc}/Slc25a1^{em1(IMPC)Kmpc}
	Slc25a1^{em1(IMPC)Kmpc}/Slc25a1⁺
	Slc25a1^{tm1b(EUCOMM)Wtsi}/Slc25a1⁺

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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