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Gene entry

LRTOMT

leucine rich transmembrane and O-methyltransferase domain containing

Chromosome
11
Cytoband
11q13.4
Variants (rsID)
7

LRTOMT is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q13.4). Its official name is “leucine rich transmembrane and O-methyltransferase domain containing”. The reference table lists 7 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs61741195Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 63
  • rs181092713Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 63
  • rs397516626Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 63
  • rs76657474Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 63
  • rs545947177Likely pathogenicsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 63|Rare genetic deafness

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.