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Human Disease and Mouse Model Detail
Human Disease Pendred Syndrome; PDS
OMIM ID: 274600
Synonyms Deafness with Goiter; Goiter-Deafness Syndrome; Hypothyroidism, Congenital, Due to Dyshormonogenesis, 2B; Thyroid Dyshormonogenesis 2B; TDH2B; Thyroid Hormonogenesis, Genetic Defect In, 2B
View all models View ALL (4) mouse models for this human disease.
Genes and
mouse models 		Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Foxi1* FOXI1* View 1 model 1:1 Homology
Slc26a4* SLC26A4* View 3 models 1:1 Homology
     Kcnj10 KCNJ10*   1:1 Homology
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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Send questions and comments to User Support. 		last database update
05/08/2013
MGI 5.13 		The Jackson Laboratory