Gene entry
INMT
indolethylamine N-methyltransferase
- Chromosome
- 7
- Cytoband
- 7p14.3
- Variants (rsID)
- 7
INMT is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7p14.3). Its official name is “indolethylamine N-methyltransferase”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
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.