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Gene entry

HAX1

HCLS1 associated protein X-1

Chromosome
1
Cytoband
1q21.3
Variants (rsID)
3

HAX1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q21.3). Its official name is “HCLS1 associated protein X-1”. The reference table lists 3 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs146152769Conflicting interpretationssingle nucleotide variantKostmann syndrome
  • rs138296453Uncertain significancesingle nucleotide variantKostmann 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.