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OTSC5 otosclerosis 5 [ Homo sapiens (human) ]

Gene ID: 317682, updated on 31-Aug-2024

Summary

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Official Symbol
OTSC5provided by HGNC
Official Full Name
otosclerosis 5provided by HGNC
Primary source
MIM:608787
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
3q22.1-q24

Bibliography

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Related articles in PubMed

  1. The phenotype of the first otosclerosis family linked to OTSC5. Pauw RJ, et al. Otol Neurotol, 2006 Apr. PMID 16639267
  2. A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24. Van Den Bogaert K, et al. J Med Genet, 2004 Jun. PMID 15173231, Free PMC Article
  3. An introduction of genetics in otosclerosis: a systematic review. Bittermann AJ, et al. Otolaryngol Head Neck Surg, 2014 Jan. PMID 24170657

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
otosclerosis 5
OMIM: 608787GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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