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Diamond Blackfan anaemia v1.22 RPL18 Zornitza Stark Phenotypes for gene: RPL18 were changed from Diamond-Blackfan anemia 18, MIM# 618310 to Diamond-Blackfan anaemia 18, MIM# 618310
Diamond Blackfan anaemia v1.21 RPL18 Zornitza Stark Publications for gene: RPL18 were set to 28280134; 32075953
Diamond Blackfan anaemia v1.20 RPL18 Zornitza Stark changed review comment from: Two recent studies add 2 unrelated families with Diamond‑Blackfan anaemia and RPL18 variants.

PMID 40510848 reports one autosomal‑recessive family with compound‑heterozygous missense variants (p.Phe43Ser, p.Asp348Asn). LIMITED evidence for this MOI.

Leschchynska2026 describes one autosomal‑dominant family (3 affected family members) with heterozygous p.G133R and VACTERL anomalies and anaemia; functional assays show protein instability and 22 % reduced protein synthesis. However, another RPS6 variant co-segregates with disease also.

Variants are absent from gnomAD.; to: Two recent studies add 2 unrelated families with Diamond‑Blackfan anaemia and RPL18 variants.

PMID 40510848 reports one autosomal‑recessive family with compound‑heterozygous missense variants (p.Phe43Ser, p.Asp348Asn). LIMITED evidence for this MOI.

Leschchynska2026 describes one autosomal‑dominant family (3 affected family members) with heterozygous p.G133R and VACTERL anomalies and anaemia; functional assays show protein instability and 22 % reduced protein synthesis. However, another RPS6 variant co-segregates with disease also.

Variants are absent from gnomAD.
Diamond Blackfan anaemia v1.20 RPL18 Zornitza Stark edited their review of gene: RPL18: Added comment: Two recent studies add 2 unrelated families with Diamond‑Blackfan anaemia and RPL18 variants.

PMID 40510848 reports one autosomal‑recessive family with compound‑heterozygous missense variants (p.Phe43Ser, p.Asp348Asn). LIMITED evidence for this MOI.

Leschchynska2026 describes one autosomal‑dominant family (3 affected family members) with heterozygous p.G133R and VACTERL anomalies and anaemia; functional assays show protein instability and 22 % reduced protein synthesis. However, another RPS6 variant co-segregates with disease also.

Variants are absent from gnomAD.; Changed publications: 28280134, 32075953, 41851260, 40510848; Changed phenotypes: Diamond-Blackfan anaemia 18, MIM# 618310
Diamond Blackfan anaemia v0.81 RPL18 Zornitza Stark Marked gene: RPL18 as ready
Diamond Blackfan anaemia v0.81 RPL18 Zornitza Stark Gene: rpl18 has been classified as Amber List (Moderate Evidence).
Diamond Blackfan anaemia v0.81 RPL18 Zornitza Stark Classified gene: RPL18 as Amber List (moderate evidence)
Diamond Blackfan anaemia v0.81 RPL18 Zornitza Stark Gene: rpl18 has been classified as Amber List (Moderate Evidence).
Diamond Blackfan anaemia v0.80 RPL18 Zornitza Stark gene: RPL18 was added
gene: RPL18 was added to Diamond Blackfan anaemia. Sources: Expert list
Mode of inheritance for gene: RPL18 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RPL18 were set to 28280134; 32075953
Phenotypes for gene: RPL18 were set to Diamond-Blackfan anemia 18, MIM# 618310
Review for gene: RPL18 was set to AMBER
Added comment: One family and a zebrafish model.
Sources: Expert list