Symbol Name ID |
Slc25a20
solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 MGI:1928738 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Irritability |
Lethargy |
Coma |
Encephalopathy |
Global developmental delay |
Seizure |
Disease(s) Associated with SLC25A20 | |||||||
carnitine-acylcarnitine translocase deficiency |
Mouse Phenotypes | cerebral arteriovenous malformation |
multiple persisting craniopharyngeal ducts |
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Availability | Mouse Genotype | ||
Slc25a20tm1a(EUCOMM)Wtsi/Slc25a20tm1a(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 05/14/2024 MGI 6.23 |
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