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HSN1B Hereditary sensory neuropathy, type IB [ Homo sapiens (human) ]

Gene ID: 378888, updated on 7-Dec-2024
Gene symbol
HSN1B
Gene description
Hereditary sensory neuropathy, type IB
See related
MIM:608088
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Location:
3p24-p22

Related articles in PubMed

  1. A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-p24. Kok C, et al. Am J Hum Genet, 2003 Sep. PMID 12870133, Free PMC Article

GeneRIFs: Gene References Into Functions

Hereditary sensory neuropathy, type IB

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  • phenotype only

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