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Symbol Name ID |
Slc12a6
solute carrier family 12, member 6 MGI:2135960 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypoplasia of the maxilla |
Microcephaly |
Brachycephaly |
Craniosynostosis |
Turricephaly |
Long fingers |
Tapered finger |
2-3 toe syndactyly |
Flexion contracture |
Scoliosis |
| Disease(s) Associated with SLC12A6 | ||||||||||
| agenesis of the corpus callosum with peripheral neuropathy |
| Mouse Phenotypes | type I spiral ligament fibrocyte degeneration |
type III spiral ligament fibrocyte degeneration |
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| Availability | Mouse Genotype | ||
| Slc12a6tm1Tjj/Slc12a6tm1Tjj | |||
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 02/23/2021 MGI 6.16 |
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