| Human Disease |
Hypoparathyroidism, Sensorineural Deafness, and Renal Disease; HDR OMIM ID: 146255 |
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| Synonyms | Barakat Syndrome; Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome; HDRS; Nephrosis, Nerve Deafness, and Hypoparathyroidism | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Gata3tm1Gsv/Gata3+ |
FVB.129(B6)-Gata3tm1Gsv | J:104653 | View |
| Gata3tm1Gsv/Gata3+ |
involves: 129S7/SvEvBrd * C57BL/6 * FVB/N | J:116235 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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