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Symbol Name ID |
Slc12a2
solute carrier family 12, member 2 MGI:101924 |
| Darker colors indicate more annotations |
| Human Phenotypes | Macrocephaly |
| Disease(s) Associated with SLC12A2 | |
| autosomal dominant nonsyndromic deafness 78 |
| Mouse Phenotypes | abnormal type II spiral ligament fibrocytes |
abnormal type IV spiral ligament fibrocytes |
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| Availability | Mouse Genotype | ||
| Slc12a2tm2Bhk/Slc12a2tm2Bhk | |||
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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