Symbol Name ID |
Nphs1
nephrosis 1, nephrin MGI:1859637 |
Darker colors indicate more annotations |
Human Phenotypes | Hyperlipidemia |
Hypoalbuminemia |
Elevated amniotic fluid alpha-fetoprotein |
Hypoproteinemia |
Edema |
Proteinuria |
Disease(s) Associated with NPHS1 | ||||||
nephrotic syndrome type 1 |
Mouse Phenotypes | edema |
increased urine protein level |
albuminuria |
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Availability | Mouse Genotype | |||
Nphs1Gt(pT1Betageo)1Ruiz/Nphs1Gt(pT1Betageo)1Ruiz | ||||
Nphs1tm1.1Tbh/Nphs1tm1.1Tbh | ||||
Nphs1tm1Ktry/Nphs1tm1Ktry | ||||
Nphs1tm1Rkl/Nphs1tm1Rkl |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/09/2024 MGI 6.23 |
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