Genetics University — Research, Education, Medical Genetics
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Gene entry

OTOG

otogelin

Chromosome
11
Cytoband
11p15.1
Variants (rsID)
36

OTOG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p15.1). Its official name is “otogelin”. The reference table lists 36 variants (rsID) for this gene.

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Clinically classified variants

24 reference-table entries with clinical significance.

  • rs11024333Benignsingle nucleotide variant
  • rs11024357Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 18B
  • rs114242958Benignsingle nucleotide variant
  • rs116947228Benignsingle nucleotide variant
  • rs143848095Benignsingle nucleotide variant
  • rs180703235Benignsingle nucleotide variant
  • rs182000850Benignsingle nucleotide variant
  • rs4757548Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 18B
  • rs61734214Benignsingle nucleotide variant
  • rs61736015Benignsingle nucleotide variant
  • rs61743165Benignsingle nucleotide variant
  • rs61997203Benignsingle nucleotide variantMeniere disease
  • rs7111528Benignsingle nucleotide variant
  • rs7112749Benignsingle nucleotide variant
  • rs7936354Benignsingle nucleotide variant
  • rs117005078Conflicting interpretationssingle nucleotide variantMeniere disease
  • rs142799217Conflicting interpretationssingle nucleotide variant
  • rs145689709Conflicting interpretationssingle nucleotide variantMeniere disease
  • rs188527711Conflicting interpretationssingle nucleotide variant
  • rs191662816Conflicting interpretationssingle nucleotide variant
  • rs61734125Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 18B
  • rs76461792Conflicting interpretationssingle nucleotide variantMeniere disease
  • rs118083195Likely benignsingle nucleotide variant
  • rs186893662Uncertain significancesingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 18B|Hearing impairment

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.