Rare anaemia

Gene: RPL17

Green List (high evidence)

RPL17 (ribosomal protein L17)
EnsemblGeneIds (GRCh38): ENSG00000265681
EnsemblGeneIds (GRCh37): ENSG00000265681
OMIM: 603661, Gene2Phenotype
RPL17 is in 3 panels

2 reviews

Achchuthan Shanmugasundram (Genomics England Curator)

Green List (high evidence)

The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.

The GMS reviewers noted that it would be appropriate to add this gene with green rating to R92 Rare anaemia in addition to R91 Cytopenia - NOT Fanconi anaemia.
Created: 20 Jan 2026, 10:48 a.m. | Last Modified: 20 Jan 2026, 10:48 a.m.
Panel Version: 3.17
Comment on phenotypes: This gene has been associated with relevant phenotype in OMIM (MIM #621262) and this OMIM record was last accessed on 20 January 2026.
Created: 20 Jan 2026, 10:45 a.m. | Last Modified: 20 Jan 2026, 10:45 a.m.
Panel Version: 3.17
Comment on list classification: As reviewed by Dmitrijs Rots, there are two unrelated pedigrees and functional evidence available in support of the association of this gene to phenotype. Hence, this can be promoted to green rating in the next GMS update.
Created: 19 Jun 2025, 5:15 p.m. | Last Modified: 19 Jun 2025, 5:15 p.m.
Panel Version: 4.16
PMID:39088281 reported two different pedigrees identified with monoallelic variants in RPL17 gene (3C>G & c.452delC/ p.(Thr151Argfs*25). Affected individuals from both pedigrees exhibited clinical features and erythroid proliferation defects consistent with Diamond-Blackfan anaemia. Individuals from first family also presented with skeletal abnormalities, which were not reported in family 2. Modelling of rpl17 deficiency in zebrafish recapitulated the major clinical features of the disorder including anaemia and micrognathia. There is also functional evidence available from lymphoblastoid cell lines (LCLs) derived from patients, which displayed a ribosomal RNA maturation defect reflecting haploinsufficiency of RPL17.

This gene has not yet been associated with relevant phenotypes either in OMIM or in Gene2Phenotype.
Created: 19 Jun 2025, 5:13 p.m. | Last Modified: 19 Jun 2025, 5:13 p.m.
Panel Version: 4.14

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Diamond-Blackfan anemia 22, OMIM:621262; Diamond-Blackfan anemia 22, MONDO:0979244

Publications

Dmitrijs Rots (Children's Clinical University Hospital)

Green List (high evidence)

PMID: 39088281 described 2 families with Diamond-Blackfan anemia & functional data. Enough evidence for the green rating.
probably gene should be added also to other panels (like limb disorders; hematological malignancies).
Sources: Literature
Created: 16 Dec 2024, 7:57 a.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Diamond-Blackfan anemia

Publications

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Diamond-Blackfan anemia 22, OMIM:621262
  • Diamond-Blackfan anemia 22, MONDO:0979244
OMIM
603661
Clinvar variants
Variants in RPL17
Penetrance
Incomplete
Publications
Panels with this gene

History Filter Activity

20 Jan 2026, Gel status: 3

Set Phenotypes

Achchuthan Shanmugasundram (Genomics England Curator)

Phenotypes for gene: RPL17 were changed from Diamond-Blackfan anemia, MONDO:0015253 to Diamond-Blackfan anemia 22, OMIM:621262; Diamond-Blackfan anemia 22, MONDO:0979244

20 Jan 2026, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes, Set penetrance

Achchuthan Shanmugasundram (Genomics England Curator)

gene: RPL17 was added gene: RPL17 was added to Rare anaemia. Sources: Expert Review Green,NHS GMS,Literature Mode of inheritance for gene: RPL17 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: RPL17 were set to 39088281 Phenotypes for gene: RPL17 were set to Diamond-Blackfan anemia, MONDO:0015253 Penetrance for gene: RPL17 were set to Incomplete