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Symbol Name ID |
Slc25a1
solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 MGI:1345283 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microretrognathia |
Narrow jaw |
Microcephaly |
Macrocephaly |
Long face |
Frontalis muscle weakness |
High palate |
| Disease(s) Associated with SLC25A1 | |||||||
| combined D-2- and L-2-hydroxyglutaric aciduria | |||||||
| congenital myasthenic syndrome |
| Mouse Phenotypes | abnormal craniofacial morphology |
abnormal cranium morphology |
abnormal facial morphology |
protruding tongue |
facial cleft |
abnormal head shape |
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| Availability | Mouse Genotype | ||||||
| Slc25a1tm1b(EUCOMM)Wtsi/Slc25a1tm1b(EUCOMM)Wtsi | |||||||
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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last database update 04/30/2024 MGI 6.23 |
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