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Gene entry

NAGA

alpha-N-acetylgalactosaminidase

Chromosome
22
Cytoband
22q13.2
Variants (rsID)
9

NAGA is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q13.2). Its official name is “alpha-N-acetylgalactosaminidase”. The reference table lists 9 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs11703233Benignsingle nucleotide variantAlpha-N-acetylgalactosaminidase deficiency type 1|Alpha-N-acetylgalactosaminidase deficiency type 2
  • rs121434529Conflicting interpretationssingle nucleotide variantAlpha-N-acetylgalactosaminidase deficiency type 1|Alpha-N-acetylgalactosaminidase deficiency|Alpha-N-acetylgalactosaminidase deficiency type 1|Alpha-N-acetylgalactosaminidase deficiency type 2|Alpha-N-acetylgalactosaminidase deficiency type 2|See cases
  • rs121434532Conflicting interpretationssingle nucleotide variantSchindler disease, type 3|Alpha-N-acetylgalactosaminidase deficiency type 1|Alpha-N-acetylgalactosaminidase deficiency type 2|Alpha-N-acetylgalactosaminidase deficiency
  • rs121434533Uncertain significancesingle nucleotide variantAlpha-N-acetylgalactosaminidase deficiency type 2|NAGA-Related Disorders

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.