Aplastic anaemia with or without paroxysmal nocturnal haemoglobinuria
Gene: GFI1EnsemblGeneIds (GRCh38): ENSG00000162676
EnsemblGeneIds (GRCh37): ENSG00000162676
OMIM: 600871, Gene2Phenotype
GFI1 is in 5 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert list
- UKGTN
- Phenotypes
-
- Inherited Bone Marrow Failure Syndromes - Neutropenia
- Severe congenital neutropenic
- OMIM
- 600871
- Clinvar variants
- Variants in GFI1
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
Added New Source
Ellen McDonagh (Genomics England Curator)GFI1 was added to Aplastic anaemia with or without paroxysmal nocturnal haemoglobinuriapanel. Source: Expert list
Set Phenotypes
Ellen McDonagh (Genomics England Curator)Phenotypes for gene GFI1 were set to Inherited Bone Marrow Failure Syndromes - Neutropenia
Set Mode of Inheritance
Ellen McDonagh (Genomics England Curator)Model of inheritance for gene GFI1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Set Mode of Inheritance
Ellen McDonagh (Genomics England Curator)Model of inheritance for gene GFI1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Set Mode of Inheritance
Ellen McDonagh (Genomics England Curator)Model of inheritance for gene GFI1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Created
Ellen McDonagh (Genomics England Curator)GFI1 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)GFI1 was added to Aplastic anaemia with or without paroxysmal nocturnal haemoglobinuriapanel. Sources: UKGTN