|
Symbol Name ID |
Slc26a2
solute carrier family 26 (sulfate transporter), member 2 MGI:892977 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Prominent occiput |
Micrognathia |
Hypoplasia of the maxilla |
Malar flattening |
Encephalocele |
Flat face |
Midface retrusion |
Short chin |
Cleft palate |
High palate |
Depressed nasal bridge |
Short nose |
| Disease(s) Associated with SLC26A2 | |||||||||||||
| achondrogenesis type IB | |||||||||||||
| atelosteogenesis | |||||||||||||
| diastrophic dysplasia | |||||||||||||
| multiple epiphyseal dysplasia 4 |
| Mouse Phenotypes | mandibular hyperostosis |
abnormal facial morphology |
protruding tongue |
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| Availability | Mouse Genotype | |||
| Slc26a2em1(IMPC)Bay/Slc26a2em1(IMPC)Bay | ||||
| Slc26a2tm1Aros/Slc26a2tm1Aros | ||||
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 03/24/2026 MGI 6.24 |
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