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Human Disease and Mouse Model Detail
Human Disease Hypothyroidism, Congenital, Nongoitrous, 2; CHNG2
OMIM ID: 218700
Synonyms Athyreotic Hypothyroidism; Hypothyroidism, Athyreotic; Hypothyroidism, Congenital, Due to Thyroid Dysgenesis; Resistance to Thyrotropin; RTSH; Thyroid Agenesis; Thyroid Dysgenesis; Thyroid Hypoplasia; Thyroid, Ectopic; Thyrotropin Resistance
View all models View ALL (3) 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
     Pax8* PAX8* View 1 model 1:1 Homology
     Foxe1* FOXE1 View 1 model 1:1 Homology
     Nkx2-5 NKX2-5*   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