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Gene entry

TMEM127

transmembrane protein 127

Chromosome
2
Cytoband
2q11.2
Variants (rsID)
7

TMEM127 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q11.2). Its official name is “transmembrane protein 127”. The reference table lists 7 variants (rsID) for this gene.

Clinically classified variants

6 reference-table entries with clinical significance.

  • rs121908823Benignsingle nucleotide variantPheochromocytoma|Hereditary cancer-predisposing syndrome|Hereditary pheochromocytoma-paraganglioma
  • rs200327514Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Hereditary pheochromocytoma-paraganglioma
  • rs750870974Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Hereditary pheochromocytoma-paraganglioma|Pheochromocytoma
  • rs758726687Likely benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Pheochromocytoma|Hereditary pheochromocytoma-paraganglioma
  • rs121908830Pathogenicsingle nucleotide variantPheochromocytoma, susceptibility to|Pheochromocytoma|Hereditary cancer-predisposing syndrome|Hereditary pheochromocytoma-paraganglioma
  • rs121908824Uncertain significancesingle nucleotide variantPheochromocytoma|Hereditary pheochromocytoma-paraganglioma|Hereditary cancer-predisposing syndrome

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.