Gene
RPL15
ribosomal protein L15
- HGNC 10306↗(opens in a new tab)
- Ensembl gene ENSG00000174748↗(opens in a new tab)
- NCBI Gene 6138↗(opens in a new tab)
Summary
- Cytogenetic location
- 3p24.2
- Coordinates
- Chromosome 3: 23,917,132–23,920,989 (GRCh38)
- Exons
- 4 exons across 3.9 kb
- Protein
- 204 amino acids
- Inheritance
- Autosomal dominant
- Also known as
- RPL10, RPLY10, RPYL10, EC45, L15, eL15
- MANE Select transcript
- ENST00000307839.10NM_002948.5
- 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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Diamond-Blackfan Anemia
- Autosomal dominant
A congenital aregenerative and often macrocytic anemia with erythroblastopenia.
- 2 GenCC submitters rate 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 RPL15 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 2.2 kb of the gene's 3.9 kb; 615 of those bases code for the protein.
How a genome test reads RPL15
2
positions in RPL15 where ClinVar classes a change as pathogenic or likely pathogenic
2 of them (100%) fall in regions short reads find hard.
- Low mappability (1 site)Regions where 100 bp or 250 bp reads cannot be placed uniquely.
- Segmental duplications (2 sites)Copies of at least 1 kb sharing at least 90% identity with another part of the genome (paralogues, pseudogenes); reads may align to the wrong copy.
A whole genome covers all 3.9 kb of RPL15, introns included, not only the 2.2 kb of exons.
Genes linked to the same conditions
- GATA1GATA binding protein 1Shares 1 condition
- HEATR3HEAT repeat containing 3Shares 1 condition
- RPL11ribosomal protein L11Shares 1 condition
- RPL26ribosomal protein L26Shares 1 condition
- RPL35Aribosomal protein L35aShares 1 condition
- RPL5ribosomal protein L5Shares 1 condition
- RPS10ribosomal protein S10Shares 1 condition
- RPS17ribosomal protein S17Shares 1 condition
- RPS19ribosomal protein S19Shares 1 condition
- RPS24ribosomal protein S24Shares 1 condition
- RPS26ribosomal protein S26Shares 1 condition
- RPS29ribosomal protein S29Shares 1 condition
Traits linked to RPL15
The Human Phenotype Ontology lists these as features of the rare conditions RPL15 can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Abnormality of the head
- Cleft lip
- Cleft soft palate
- High palate
- Short neck
- Webbed neck
- Abnormally small head
- Depressed nasal bridge
Show 4 more traits
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.). RPL15 gene: ribosomal protein L15. Retrieved 17 October 2026, from https://dantelabs.com/genes/rpl15
Dante Labs. RPL15 gene: ribosomal protein L15 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/rpl15
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