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OTSC7 otosclerosis 7 [ Homo sapiens (human) ]

Gene ID: 399516, updated on 31-Aug-2024

Summary

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Official Symbol
OTSC7provided by HGNC
Official Full Name
otosclerosis 7provided by HGNC
Primary source
MIM:611572
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:
6q13-q16.1

Bibliography

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Related articles in PubMed

  1. Phenotype description of a Dutch otosclerosis family with suggestive linkage to OTSC7. Pauw RJ, et al. Am J Med Genet A, 2007 Jul 15. PMID 17568406
  2. A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1. Thys M, et al. Eur J Hum Genet, 2007 Mar. PMID 17213839

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Study reports on a clinical investigation of a Dutch family that shows suggestive linkage to OTSC7.
    Title: Phenotype description of a Dutch otosclerosis family with suggestive linkage to OTSC7.
  2. Maps to chromosome 6q13-16.1
    Title: A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1.
Submit: New GeneRIF Correction

Phenotypes

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Associated conditions

Description Tests
otosclerosis 7
OMIM: 611572GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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