Genetics University — Research, Education, Medical Genetics
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Gene entry

NFAT5

nuclear factor of activated T cells 5

Chromosome
16
Cytoband
16q22.1
Variants (rsID)
15

NFAT5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q22.1). Its official name is “nuclear factor of activated T cells 5”. The reference table lists 15 variants (rsID) for this gene.

Clinically classified variants

3 reference-table entries with clinical significance.

  • rs144343499Benignsingle nucleotide variantImmunodeficiency
  • rs145602190Benignsingle nucleotide variantImmunodeficiency
  • rs56368098Benignsingle nucleotide variantImmunodeficiency

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.