Gene entry
OSTM1
osteoclastogenesis associated transmembrane protein 1
- Chromosome
- 6
- Cytoband
- 6q21
- Variants (rsID)
- 8
OSTM1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q21). Its official name is “osteoclastogenesis associated transmembrane protein 1”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs141735624Benignsingle nucleotide variantAutosomal recessive osteopetrosis 5
- rs9480830Benignsingle nucleotide variantAutosomal recessive osteopetrosis 5
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.