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Symbol
Name
ID

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

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Microretrognathia	Narrow jaw	Microcephaly	Macrocephaly	Congenital hip dislocation	Arthrogryposis multiplex congenita	Joint hypermobility	Pectus carinatum	Kyphoscoliosis	Neuropathic spinal arthropathy	Spinal rigidity
Disease(s) Associated with SLC25A1	Microretrognathia	Narrow jaw	Microcephaly	Macrocephaly	Congenital hip dislocation	Arthrogryposis multiplex congenita	Joint hypermobility	Pectus carinatum	Kyphoscoliosis	Neuropathic spinal arthropathy	Spinal rigidity
combined D-2- and L-2-hydroxyglutaric aciduria
congenital myasthenic syndrome

Mouse Phenotypes		abnormal cranium morphology
Availability	Mouse Genotype	abnormal cranium morphology
	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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