Congenital anaemias

Gene: IFNG

Red List (low evidence)

IFNG (interferon gamma)
EnsemblGeneIds (GRCh38): ENSG00000111537
EnsemblGeneIds (GRCh37): ENSG00000111537
OMIM: 147570, Gene2Phenotype
IFNG is in 5 panels

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Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Illumina TruGenome Clinical Sequencing Services
Phenotypes
  • Aplastic Anemia
OMIM
147570
Clinvar variants
Variants in IFNG
Penetrance
Complete
Panels with this gene

History Filter Activity

30 Sep 2015, Gel status: 1

Set Mode of Inheritance

Ellen McDonagh (Genomics England Curator)

Model of inheritance for gene IFNG was set to BIALLELIC, autosomal or pseudoautosomal

30 Sep 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

IFNG was added to Congenital anaemiaspanel. Source: Illumina TruGenome Clinical Sequencing Services

28 Apr 2015, Gel status: 1

Added New Source

GEL ()

IFNG was added to Congenital anaemiaspanel. Sources: Illumina TruGenome Clinical Sequencing Services