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Human Disease and Mouse Model Detail
Human Disease Neuropathy, Hereditary Sensory and Autonomic, Type IA; HSAN1A
OMIM ID: 162400
Human Phenotype Ontology associations
Synonyms Hsan1; Hsan IA; Hsn IA; Neuropathy, Hereditary Sensory and Autonomic; Neuropathy, Hereditary Sensory Radicular, Autosomal Dominant, Type 1a; Neuropathy, Hereditary Sensory, Type IA; HSN1A
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
     SPTLC1* Sptlc1 View 1 model HomoloGene and HGNC
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(CAG-SPTLC1*C133W)8EAmcc View 1 model
References Disease References using Mouse Models (2)

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