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Symbol Name ID |
Slc46a1
solute carrier family 46, member 1 MGI:1098733 |
| Darker colors indicate more annotations |
| Human Phenotypes | Anorexia |
Feeding difficulties in infancy |
Atypical behavior |
| Disease(s) Associated with SLC46A1 | |||
| hereditary folate malabsorption |
| Mouse Phenotypes | decreased locomotor activity |
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| Availability | Mouse Genotype | |
| Slc46a1tm1b(KOMP)Mbp/Slc46a1tm1b(KOMP)Mbp | ||
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 04/16/2024 MGI 6.23 |
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