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Gene entry

TMEM231

transmembrane protein 231

Chromosome
16
Cytoband
16q23.1
Variants (rsID)
10

TMEM231 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q23.1). Its official name is “transmembrane protein 231”. The reference table lists 10 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs149888762Conflicting interpretationssingle nucleotide variantMeckel syndrome, type 11|Joubert syndrome 20
  • rs202215735Conflicting interpretationssingle nucleotide variantJoubert syndrome 20|Meckel syndrome, type 11
  • rs201036290Likely benignsingle nucleotide variantMeckel syndrome, type 11|Joubert syndrome 20
  • rs199605221Uncertain significancesingle nucleotide variantJoubert syndrome 20|Meckel syndrome, type 11

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.