Symbol Name ID |
Slc26a4
solute carrier family 26, member 4 MGI:1346029 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hyperparathyroidism |
Goiter |
Thyroid carcinoma |
Hypothyroidism |
Compensated hypothyroidism |
Disease(s) Associated with SLC26A4 | |||||
autosomal recessive nonsyndromic deafness 4 | |||||
Pendred Syndrome |
Mouse Phenotypes | endocrine/exocrine gland phenotype |
abnormal thyroid gland morphology |
abnormal thyroid follicle morphology |
testicular atrophy |
|
Availability | Mouse Genotype | ||||
Slc26a4loop/Slc26a4loop | |||||
Slc26a4pdsm/Slc26a4pdsm | * | ||||
Slc26a4tm1.1Dontu/Slc26a4tm1.1Dontu | * | ||||
Slc26a4tm1Egr/Slc26a4tm1Egr | * | ||||
Slc26a4tm2.1Dontu/Slc26a4tm2.1Dontu | * | ||||
Slc26a4tm1.1Dontu/Slc26a4tm2.1Dontu | * |
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 04/30/2024 MGI 6.23 |
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