| Human Disease |
Thiamine-Responsive Megaloblastic Anemia Syndrome; TRMA OMIM ID: 249270 |
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| Synonyms | Megaloblastic Anemia, Thiamine-Responsive, with Diabetes Mellitus and Sensorineural Deafness; Rogers Syndrome; Thiamine Metabolism Dysfunction Syndrome 1 (megaloblastic Anemia, Diabetes Mellitus, and Deafness Type); THMD1; Thiamine-Responsive Anemia Syndrome; Thiamine-Responsive Myelodysplasia | |||||||||||||||||||||
| 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 |
| Slc19a2tm1Gelb/Slc19a2tm1Gelb |
involves: 129X1/SvJ | J:79974 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Slc19a2tm1Ejn/Slc19a2tm1Ejn |
involves: 129S4/SvJae * 129S6/SvEvTac | J:101675 | 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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