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Human Disease and Mouse Model Detail
Human Disease Senior-Loken Syndrome 1; SLSN1
OMIM ID: 266900
Human Phenotype Ontology associations
Synonyms Juvenile Nephronophthisis with Leber Amaurosis; Loken-Senior Syndrome; Renal Dysplasia and Retinal Aplasia; Renal-Retinal Syndrome; Senior-Loken Syndrome; Senior-Loken Syndrome
View all models View ALL (1) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     TMEM218 Tmem218* View 1 model HomoloGene and HGNC
     NPHP1* Nphp1   HomoloGene and HGNC
References Disease References using Mouse Models (1)

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
MGI 6.07
The Jackson Laboratory