| Human Disease |
Nephrotic Syndrome, Type 2; NPHS2 OMIM ID: 600995 |
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| Synonyms | Nephrotic Syndrome, Steroid-Resistant, Autosomal Recessive; SRN1 | ||||||||||||||||||||||||||||||||
| View all models | View ALL (5) 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 |
| Nphs2tm1Antc/Nphs2tm1Antc |
129-Nphs2tm1Antc | J:87577 | View |
| Nphs2tm1Antc/Nphs2tm1Antc |
involves: 129 * C57BL/6J | J:87577 | View |
| Nphs2tm1Antc/Nphs2tm3.1Antc Tg(CAG-cre/Esr1*)86Lbgn/0 |
involves: 129 * C57BL/6 * DBA | J:166320 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Arhgdiatm1Ytk/Arhgdiatm1Ytk |
involves: 129S/SvEv * C57BL/6 * DBA | J:57995 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Mpv17/Mpv17 |
involves: CFW | J:10661, J:108252 | 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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