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Symbol
Name
ID
Slc26a4
solute carrier family 26, member 4
MGI:1346029
Phenotype annotations related to endocrine/exocrine glands
*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 *

Contributing Projects:
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
The Jackson Laboratory