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| Thalassaemia and other haemoglobinopathies v1.9 | HBG2 | Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: HBG2. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Thalassaemia and other haemoglobinopathies v1.9 | HBG2 | Sarah Leigh reviewed gene: HBG2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Thalassaemia and other haemoglobinopathies v1.8 | HBG2 |
Achchuthan Shanmugasundram Source Expert Review Green was added to HBG2. Rating Changed from Amber List (moderate evidence) to Green List (high evidence) |
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| Thalassaemia and other haemoglobinopathies v1.7 | HBG2 | Arina Puzriakova Classified gene: HBG2 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Thalassaemia and other haemoglobinopathies v1.7 | HBG2 | Arina Puzriakova Gene: hbg2 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Thalassaemia and other haemoglobinopathies v1.6 | HBG2 |
Arina Puzriakova gene: HBG2 was added gene: HBG2 was added to Thalassaemia and other haemoglobinopathies. Sources: NHS GMS Q4_23_promote_green tags were added to gene: HBG2. Mode of inheritance for gene: HBG2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Review for gene: HBG2 was set to GREEN Added comment: This gene has been added to the panel at the request of the NHSE specialist group. There is sufficient evidence to promote this gene to Green at the next GMS panel update. ----- Copied review below from Arianna Tucci (UCL) on Cytopenias and congenital anaemias (159) panel for HBG1 gene (also relevant to HBG2): "delta beta thalassemia can result from deletions within or encompassing the beta-globin gene cluster (see HBB, 141900) on chromosome 11p15, including deletions that also encompass the delta-globin gene (142000), or from point mutations in the promoter regions of either the HBG1 (142200) or the HBG2 (142250) gene" Sources: NHS GMS |
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| Thalassaemia and other haemoglobinopathies v1.4 | HBG1 |
Arina Puzriakova gene: HBG1 was added gene: HBG1 was added to Thalassaemia and other haemoglobinopathies. Sources: NHS GMS Q4_23_promote_green tags were added to gene: HBG1. Mode of inheritance for gene: HBG1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Review for gene: HBG1 was set to GREEN Added comment: This gene has been added to the panel at the request of the NHSE specialist group. There is sufficient evidence to promote this gene to Green at the next GMS panel update. ----- Copied review below from Arianna Tucci (UCL) on Cytopenias and congenital anaemias (159) panel: "delta beta thalassemia can result from deletions within or encompassing the beta-globin gene cluster (see HBB, 141900) on chromosome 11p15, including deletions that also encompass the delta-globin gene (142000), or from point mutations in the promoter regions of either the HBG1 (142200) or the HBG2 (142250) gene" Sources: NHS GMS |
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