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| Haematological malignancies v0.126 | RPL27 | Zornitza Stark Marked gene: RPL27 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.126 | RPL27 | Zornitza Stark Gene: rpl27 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.126 | RPL27 | Zornitza Stark Phenotypes for gene: RPL27 were changed from Osteosarcoma, soft tissue sarcomas; Diamond Blackfan Anemia; MDS, AML; Class: BM failure syndrome (typ AR) to Osteosarcoma, soft tissue sarcomas; Diamond-Blackfan anaemia 16, MIM# 617408; MDS, AML; Class: BM failure syndrome (typ AR) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.125 | RPL27 | Zornitza Stark Publications for gene: RPL27 were set to 28297620 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.124 | RPL27 | Zornitza Stark Mode of inheritance for gene: RPL27 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.123 | RPL27 | Zornitza Stark Classified gene: RPL27 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.123 | RPL27 | Zornitza Stark Gene: rpl27 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.122 | RPL27 | Zornitza Stark edited their review of gene: RPL27: Added comment: PMID 38988374 reports an individual from a second unrelated family with a de novo splice‑site RPL27 variant and a DBA phenotype.; Changed rating: AMBER; Changed publications: 25424902, 38988374; Changed phenotypes: Diamond-Blackfan anaemia 16, MIM# 617408 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.70 | Bryony Thompson Added reviews for gene RPL27 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Haematological malignancies v0.0 | RPL27 |
Bryony Thompson gene: RPL27 was added gene: RPL27 was added to Haematological malignancies cancer susceptibility. Sources: Expert Review Red,Curated sources,NHS GMS Mode of inheritance for gene: RPL27 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: RPL27 were set to 28297620 Phenotypes for gene: RPL27 were set to Osteosarcoma, soft tissue sarcomas; Diamond Blackfan Anemia; MDS, AML; Class: BM failure syndrome (typ AR) |
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