Haematological malignancies cancer susceptibility
Gene: HAX1EnsemblGeneIds (GRCh38): ENSG00000143575
EnsemblGeneIds (GRCh37): ENSG00000143575
OMIM: 605998, Gene2Phenotype
HAX1 is in 10 panels
1 review
Clare Turnbull (Queen Mary University London)
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Curated sources
- Phenotypes
-
- Class: miscellaneous
- MDS, AML
- OMIM
- 605998
- Clinvar variants
- Variants in HAX1
- Penetrance
- Complete
- Publications
- Panels with this gene
-
- Intellectual disability
- Haematological malignancies for rare disease
- Cytopenia - NOT Fanconi anaemia
- Cytopenias and congenital anaemias
- Primary immunodeficiency or monogenic inflammatory bowel disease
- DDG2P
- Haematological malignancies cancer susceptibility
- Early onset or syndromic epilepsy
- Fetal anomalies
- COVID-19 research
History Filter Activity
Panel promoted to version 1.0
Louise Daugherty (Genomics England Curator)Ellen McDonagh: Comment on mode of inheritance
Added New Source
Ellen McDonagh (Genomics England Curator)Expert Review Green was added to HAX1. Panel: Haematological malignancies pertinent cancer susceptibility
Added New Source
Ellen McDonagh (Genomics England Curator)HAX1 was added to Haematological malignanciespanel. Sources: Curated sources
Created
Ellen McDonagh (Genomics England Curator)HAX1 was created by ellenmcdonagh