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Human Disease and Mouse Model Detail
Human Disease Neuropathy, Hereditary Sensory and Autonomic, Type IIA; HSAN2A
OMIM ID: 201300
Synonyms Acroosteolysis, Giaccai Type; Acroosteolysis, Neurogenic; Hsan IIA; Hsn IIA; Morvan Disease; Neuropathy, Congenital Sensory; Neuropathy, Hereditary Sensory and Autonomic; Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive; Neuropathy, Hereditary Sensory, Type IIA; HSN2A; Neuropathy, Progressive Sensory, of Children
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
     Wnk1 WNK1*   1:1 Homology

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
08/26/2014
MGI 5.19
The Jackson Laboratory