| Human Disease |
Allan-Herndon-Dudley Syndrome; AHDS OMIM ID: 300523 |
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| Synonyms | Allan-Herndon Syndrome; Mental Retardation and Muscular Atrophy; Mental Retardation, X-Linked, with Hypotonia; Monocarboxylate Transporter 8 Deficiency; T3 Resistance; Triiodothyronine Resistance | |||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Slc16a2tm1Dgen/Y |
either: (involves: C57BL/6N) or (involves: NMRI) | J:120737 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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