Gene
PRKAR1B
protein kinase cAMP-dependent type I regulatory subunit beta
- HGNC 9390↗(opens in a new tab)
- Ensembl gene ENSG00000188191↗(opens in a new tab)
- NCBI Gene 5575↗(opens in a new tab)
Summary
- Cytogenetic location
- 7p22.3
- Coordinates
- Chromosome 7: 549,198–727,281 (GRCh38)
- Exons
- 11 exons across 178.1 kb
- Protein
- 381 amino acids
- MANE Select transcript
- ENST00000537384.6NM_001164760.2
- 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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Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads PRKAR1B yet. The test sequences your whole genome, so your data includes it all the same.
How PRKAR1B 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 2.5 kb of the gene's 178.1 kb; 1,146 of those bases code for the protein.
How a genome test reads PRKAR1B
2
positions in PRKAR1B 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 178.1 kb of PRKAR1B, introns included, not only the 2.5 kb of exons.
Traits linked to PRKAR1B
The Human Phenotype Ontology lists these as features of the rare conditions PRKAR1B can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Attention deficit
- Autism spectrum disorder
- Delayed speech and language development
- Dementia
- Global developmental delay
- Speech apraxia
- Abnormal neuron shape
- Frontotemporal dementia
Show 27 more traits
- Inappropriate behavior
- Memory impairment
- Progressive degeneration of movement
- Aggressive behavior
- Anxiety
- Balance impairment
- Diffuse cerebral atrophy
- Falls
- Impaired visuospatial constructive cognition
- Inertia
- Lack of feeling, emotion, interest
- Language impairment
- Obstructive sleep apnea
- Parkinsonism
- Short attention span
- Short stepped shuffling walk
- Shuffled walk
- Slow movements
- Epilepsy
- Frontotemporal cerebral atrophy
- Happy demeanor
- Hemidystonia
- Recurrent hand flapping
- Sensory seeking
- Tremor
- Motor neuron atrophy
- Spinocerebellar tract degeneration
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.
- 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.). PRKAR1B gene: protein kinase cAMP-dependent type I regulatory subunit beta. Retrieved 16 October 2026, from https://dantelabs.com/genes/prkar1b
Dante Labs. PRKAR1B gene: protein kinase cAMP-dependent type I regulatory subunit beta [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/prkar1b
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