Gene entry
TCIRG1
T cell immune regulator 1, ATPase H+ transporting V0 subunit a3
- Chromosome
- 11
- Cytoband
- 11q13.2
- Variants (rsID)
- 12
TCIRG1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q13.2). Its official name is “T cell immune regulator 1, ATPase H+ transporting V0 subunit a3”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs36027301Benignsingle nucleotide variantAutosomal recessive osteopetrosis 1|Increased bone mineral density
- rs140963213Conflicting interpretationssingle nucleotide variantAutosomal recessive osteopetrosis 1|Increased bone mineral density
- rs34227834Conflicting interpretationssingle nucleotide variantAutosomal recessive osteopetrosis 1
- rs139617644Pathogenicsingle nucleotide variantAutosomal recessive osteopetrosis 1|Osteopetrosis
- rs751881962Pathogenicsingle nucleotide variantAutosomal recessive osteopetrosis 1
- rs140191063Uncertain significancesingle nucleotide variantAutosomal recessive osteopetrosis 1
- rs150260808Uncertain significancesingle nucleotide variantAutosomal recessive osteopetrosis 1
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.