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Gene entry

PROKR2

prokineticin receptor 2

Chromosome
20
Cytoband
20p12.3
Variants (rsID)
14

PROKR2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p12.3). Its official name is “prokineticin receptor 2”. The reference table lists 14 variants (rsID) for this gene.

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Clinically classified variants

7 reference-table entries with clinical significance.

  • rs78861628Benignsingle nucleotide variantHypogonadotropic hypogonadism 3 with or without anosmia
  • rs141090506Conflicting interpretationssingle nucleotide variantHypogonadotropic hypogonadism 3 without anosmia|Hypogonadotropic hypogonadism 3 with or without anosmia
  • rs201835496Conflicting interpretationssingle nucleotide variantHypogonadotropic hypogonadism 3 with or without anosmia
  • rs202203360Conflicting interpretationssingle nucleotide variantHypogonadotropic hypogonadism 3 with or without anosmia
  • rs587777834Conflicting interpretationsDeletionHypogonadotropic hypogonadism 3 with or without anosmia|Inborn genetic diseases|Hypogonadotropic hypogonadism 2 with or without anosmia
  • rs74315416Conflicting interpretationssingle nucleotide variantHypogonadotropic hypogonadism 3 with or without anosmia|Infertility
  • rs376239580Likely pathogenicsingle nucleotide variantHypogonadotropic hypogonadism 7 with or without anosmia|Hypogonadotropic hypogonadism 3 with or without anosmia

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.