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Symbol Name ID |
Slc4a2
solute carrier family 4 (anion exchanger), member 2 MGI:109351 |
| Darker colors indicate more annotations |
| Human Phenotypes | Craniosynostosis |
Macrocephaly |
Delayed eruption of teeth |
Premature loss of primary teeth |
Chronic rhinitis |
| Disease(s) Associated with SLC4A2 | |||||
| osteopetrosis |
| Mouse Phenotypes | failure of tooth eruption |
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| Availability | Mouse Genotype | |
| Slc4a2tm1Ges/Slc4a2tm1Ges | ||
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 04/09/2024 MGI 6.23 |
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