Gene
PROK2
prokineticin 2
- HGNC 18455↗(opens in a new tab)
- Ensembl gene ENSG00000163421↗(opens in a new tab)
- NCBI Gene 60675↗(opens in a new tab)
Summary
- Cytogenetic location
- 3p13
- Coordinates
- Chromosome 3: 71,771,655–71,785,148 (GRCh38)
- Exons
- 4 exons across 13.5 kb
- Protein
- 129 amino acids
- Also known as
- PK2, BV8, MIT1, KAL4
- MANE Select transcript
- ENST00000295619.4NM_001126128.2
- 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
- 3 GenCC submitters rate it definitive or strong
How PROK2 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 1.6 kb of the gene's 13.5 kb; 390 of those bases code for the protein.
How a genome test reads PROK2
3
positions in PROK2 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 13.5 kb of PROK2, introns included, not only the 1.6 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 PROK2
The Human Phenotype Ontology lists these as features of the rare conditions PROK2 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
- Hypermobility of all joints
- Low muscle tone
- Muscle weakness
Show 2 more traits
Abnormality of the nervous system
- Aplasia of the olfactory bulb
- Anxiety
- Depression
- Abnormal gait
- Ataxia
- Difficulty articulating speech
- Epilepsy
- Hand mirror movements
Show 2 more traits
Abnormality of the endocrine system
- Absence of pubertal development
- Hypogonadotropic hypogonadism
- Absence of secondary sex characteristics
- Anterior hypopituitarism
- Decreased function of male gonad
- Decreased serum testosterone level
- Delayed puberty
- Female hypogonadism
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.). PROK2 gene: prokineticin 2. Retrieved 16 October 2026, from https://dantelabs.com/genes/prok2
Dante Labs. PROK2 gene: prokineticin 2 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/prok2
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