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Human Disease and Mouse Model Detail
Human Disease Nephrotic Syndrome, Type 1; NPHS1
OMIM ID: 256300
Synonyms Finnish Congenital Nephrosis; CNF; Nephrotic Syndrome; Nephrotic Syndrome, Congenital
View all models View ALL (4) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Nphs1* NPHS1* View 4 models 1:1 Homology
References Disease References using Mouse Models (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/08/2014
MGI 5.20
The Jackson Laboratory