| Human Disease |
Pseudohypoaldosteronism, Type I, Autosomal Recessive; PHA1B OMIM ID: 264350 |
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| Synonyms | Pha I, Autosomal Recessive | ||||||||||||||||||||||||||||||||
| 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 |
| Scnn1btm1Wsh/Scnn1btm1Wsh |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:53058 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Scnn1gtm1Bhk/Scnn1gtm1Bhk |
involves: 129P2/OlaHsd * C57BL/6 * DBA/2 | J:50528 | 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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