Gene
APOA2
apolipoprotein A2
- HGNC 601↗(opens in a new tab)
- Ensembl gene ENSG00000158874↗(opens in a new tab)
- NCBI Gene 336↗(opens in a new tab)
Summary
- Cytogenetic location
- 1q23.3
- Coordinates
- Chromosome 1: 161,222,292–161,223,628 (GRCh38)
- Exons
- 4 exons across 1.3 kb
- Protein
- 100 amino acids
- MANE Select transcript
- ENST00000367990.7NM_001643.2
- 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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How APOA2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
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 0.5 kb of the gene's 1.3 kb; 303 of those bases code for the protein.
Traits linked to APOA2
The Human Phenotype Ontology lists these as features of the rare conditions APOA2 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.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
Cite this page
Dante Labs. (n.d.). APOA2 gene: apolipoprotein A2. Retrieved 17 October 2026, from https://dantelabs.com/genes/apoa2
Dante Labs. APOA2 gene: apolipoprotein A2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/apoa2
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