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Symbol Name ID |
Slc25a26
solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26 MGI:1914832 |
| Darker colors indicate more annotations |
| Human Phenotypes | Polyhydramnios |
Decreased fetal movement |
| Disease(s) Associated with SLC25A26 | ||
| combined oxidative phosphorylation deficiency 28 |
| Mouse Phenotypes | embryonic growth retardation |
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| Availability | Mouse Genotype | |
| Slc25a26Tn(sb-T/MPT/eGFP)1.32Dla/Slc25a26Tn(sb-T/MPT/eGFP)1.32Dla | ||
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 05/28/2024 MGI 6.13 |
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