Gene
PROKR2
prokineticin receptor 2
- HGNC 15836↗(opens in a new tab)
- Ensembl gene ENSG00000101292↗(opens in a new tab)
- NCBI Gene 128674↗(opens in a new tab)
Summary
- Cytogenetic location
- 20p12.3
- Coordinates
- Chromosome 20: 5,299,218–5,316,954 (GRCh38)
- Exons
- 3 exons across 17.7 kb
- Protein
- 384 amino acids
- Also known as
- GPR73b, PKR2, GPRg2, dJ680N4.3
- Previous symbols
- GPR73L1, KAL3
- MANE Select transcript
- ENST00000678254.1NM_144773.4
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Hypogonadotropic Hypogonadism
Abnormal ovarian or testicular function due to insufficient hormonal stimulation from the hypothalamic-pituitary axis.
- ClinGen rates the link definitive
- 5 GenCC submitters rate it definitive or strong
How PROKR2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 4.4 kb of the gene's 17.7 kb; 1,155 of those bases code for the protein.
How a genome test reads PROKR2
13
positions in PROKR2 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 17.7 kb of PROKR2, introns included, not only the 4.4 kb of exons.
Genes linked to the same conditions
- ANOS1anosmin 1Shares 1 condition
- ARHGAP35Rho GTPase activating protein 35Shares 1 condition
- CHD7chromodomain helicase DNA binding protein 7Shares 1 condition
- CPEcarboxypeptidase EShares 1 condition
- DCAF17DDB1 and CUL4 associated factor 17Shares 1 condition
- FEZF1FEZ family zinc finger 1Shares 1 condition
- FGF17fibroblast growth factor 17Shares 1 condition
- FGF8fibroblast growth factor 8Shares 1 condition
- FGFR1fibroblast growth factor receptor 1Shares 1 condition
- FOXA2forkhead box A2Shares 1 condition
- FSHBfollicle stimulating hormone subunit betaShares 1 condition
- GH1growth hormone 1Shares 1 condition
Traits linked to PROKR2
The Human Phenotype Ontology lists these as features of the rare conditions PROKR2 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the musculoskeletal system
- Delayed bone maturation
- Low solidness and mass of the bones
- Osteopenia
- Osteoporosis
- Abnormal skeletal development
- Funnel chest
- Hypermobility of all joints
- Low muscle tone
Show 3 more traits
Abnormality of the eye
- Optic nerve hypoplasia
- Septo-optic dysplasia
- Visual impairment
- Cross-eyed
- Involuntary, rapid, rhythmic eye movements
- Abnormal color vision
- Drooping upper eyelid
- Wide-set eyes
Show 1 more trait
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). PROKR2 gene: prokineticin receptor 2. Retrieved 16 October 2026, from https://dantelabs.com/genes/prokr2
Dante Labs. PROKR2 gene: prokineticin receptor 2 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/prokr2
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