Rare anaemia
Gene: RPL17EnsemblGeneIds (GRCh38): ENSG00000265681
EnsemblGeneIds (GRCh37): ENSG00000265681
OMIM: 603661, Gene2Phenotype
RPL17 is in 3 panels
2 reviews
Achchuthan Shanmugasundram (Genomics England Curator)
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)
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: LiteratureCreated: 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
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
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