Gene
GPR161
G protein-coupled receptor 161
- HGNC 23694↗(opens in a new tab)
- Ensembl gene ENSG00000143147↗(opens in a new tab)
- NCBI Gene 23432↗(opens in a new tab)
Summary
- Cytogenetic location
- 1q24.2
- Coordinates
- Chromosome 1: 168,079,542–168,136,930 (GRCh38)
- Exons
- 6 exons across 57.4 kb
- Protein
- 529 amino acids
- Inheritance
- Autosomal dominant
- Also known as
- RE2
- MANE Select transcript
- ENST00000682931.1NM_001375883.1
- 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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Medulloblastoma
- GPR161-related medulloblastoma predispositionAutosomal dominant
GPR161 variants that predispose to sonic hedgehog-type medulloblastoma in early childhood.
- ClinGen rates the link strong
- 1 GenCC submitter rates it definitive or strong
What knowing changes
Awareness of neurological symptoms in young children and consideration of brain MRI surveillance.
- Autosomal dominant
- 1 GenCC submitter rates it definitive or strong
Inheritance
- Autosomal dominant
- One changed copy, from either parent, is enough. A parent who has one passes it on to each child with a one-in-two chance.
How GPR161 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 7.8 kb of the gene's 57.4 kb; 1,590 of those bases code for the protein.
How a genome test reads GPR161
2
positions in GPR161 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 57.4 kb of GPR161, introns included, not only the 7.8 kb of exons.
Genes linked to the same conditions
Traits linked to GPR161
The Human Phenotype Ontology lists these as features of the rare conditions GPR161 can cause. Each trait's page lists the other genes linked to it.
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.). GPR161 gene: G protein-coupled receptor 161. Retrieved 17 October 2026, from https://dantelabs.com/genes/gpr161
Dante Labs. GPR161 gene: G protein-coupled receptor 161 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/gpr161
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