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Symbol
Name
ID

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

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Polyhydramnios	Decreased fetal movement
Disease(s) Associated with SLC25A1	Polyhydramnios	Decreased fetal movement
congenital myasthenic syndrome

Mouse Phenotypes		abnormal embryo development	embryonic growth retardation	abnormal embryo size	abnormal neural tube closure
Availability	Mouse Genotype	abnormal embryo development	embryonic growth retardation	abnormal embryo size	abnormal neural tube closure
	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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