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Gene entry

SRPX2

sushi repeat containing protein X-linked 2

Chromosome
X
Cytoband
Xq22.1
Variants (rsID)
22

SRPX2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq22.1). Its official name is “sushi repeat containing protein X-linked 2”. The reference table lists 22 variants (rsID) for this gene.

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Clinically classified variants

9 reference-table entries with clinical significance.

  • rs146051561Benignsingle nucleotide variantRolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
  • rs148735447Benignsingle nucleotide variantRolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
  • rs142719253Conflicting interpretationssingle nucleotide variantRolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
  • rs149051060Conflicting interpretationssingle nucleotide variantRolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
  • rs200784551Conflicting interpretationssingle nucleotide variantRolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
  • rs369663551Conflicting interpretationssingle nucleotide variantRolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
  • rs73636611Conflicting interpretationssingle nucleotide variantRolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
  • rs121918364Uncertain significancesingle nucleotide variantRolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
  • rs183378773Uncertain significancesingle nucleotide variantRolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked

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.