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Human Disease and Mouse Model Detail
Human Disease

Term: Neuropathy, Hereditary Sensory, Type IE; HSN1E
OMIM ID: 614116

Synonyms Hsn IE; Neuropathy, Hereditary Sensory, with Hearing Loss and Dementia
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Dnmt1 DNMT1
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory