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Gene entry

AP5Z1

adaptor related protein complex 5 subunit zeta 1

Chromosome
7
Cytoband
7p22.1
Variants (rsID)
15

AP5Z1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7p22.1). Its official name is “adaptor related protein complex 5 subunit zeta 1”. The reference table lists 15 variants (rsID) for this gene.

Clinically classified variants

9 reference-table entries with clinical significance.

  • rs117666541Benignsingle nucleotide variantHereditary spastic paraplegia 48|Hereditary spastic paraplegia
  • rs11772411Benignsingle nucleotide variantHereditary spastic paraplegia 48|Hereditary spastic paraplegia
  • rs146665638Benignsingle nucleotide variantHereditary spastic paraplegia 48
  • rs184752711Benignsingle nucleotide variantHereditary spastic paraplegia 48|Hereditary spastic paraplegia
  • rs77890266Benignsingle nucleotide variantHereditary spastic paraplegia 48|Hereditary spastic paraplegia
  • rs200957609Conflicting interpretationssingle nucleotide variantHereditary spastic paraplegia 48|Hereditary spastic paraplegia
  • rs12154696Likely benignsingle nucleotide variantHereditary spastic paraplegia 48
  • rs145463842Uncertain significancesingle nucleotide variantHereditary spastic paraplegia|Hereditary spastic paraplegia 48
  • rs147369435Uncertain significancesingle nucleotide variantHereditary spastic paraplegia 48

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.