Gene entry
TMPO
thymopoietin
- Chromosome
- 12
- Cytoband
- 12q23.1
- Variants (rsID)
- 23
TMPO is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q23.1). Its official name is “thymopoietin”. The reference table lists 23 variants (rsID) for this gene.
Clinically classified variants
13 reference-table entries with clinical significance.
- rs114939776Benignsingle nucleotide variantLoeys-Dietz syndrome 2|Cardiovascular phenotype
- rs138790561Benignsingle nucleotide variantCardiovascular phenotype|Loeys-Dietz syndrome 2
- rs145703021Benignsingle nucleotide variantLoeys-Dietz syndrome 2|Cardiovascular phenotype|Primary dilated cardiomyopathy
- rs397516844Benignsingle nucleotide variantLoeys-Dietz syndrome 2
- rs80325832Benignsingle nucleotide variantCardiovascular phenotype|Loeys-Dietz syndrome 2
- rs138295270Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Loeys-Dietz syndrome 2
- rs141443652Conflicting interpretationssingle nucleotide variantPrimary dilated cardiomyopathy|Dilated cardiomyopathy 1T|Cardiovascular phenotype|Amyloidosis|Arrhythmogenic right ventricular cardiomyopathy|Loeys-Dietz syndrome 2
- rs17028450Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1T|Primary dilated cardiomyopathy|Loeys-Dietz syndrome 2|Cardiovascular phenotype|Hypertrophic cardiomyopathy 25
- rs200420073Conflicting interpretationssingle nucleotide variant
- rs34150443Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Loeys-Dietz syndrome 2
- rs141387097Likely benignsingle nucleotide variantLoeys-Dietz syndrome 2|Cardiovascular phenotype
- rs202035749Likely benignsingle nucleotide variantArrhythmogenic right ventricular cardiomyopathy|Loeys-Dietz syndrome 2
- rs727504659Likely benignsingle nucleotide variantCardiovascular phenotype|Loeys-Dietz syndrome 2
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.