This Panel is marked as Internal
Anaemias and red cell disorders
Gene: ANKRD26
ANKRD26 (ankyrin repeat domain 26)
EnsemblGeneIds (GRCh38): ENSG00000107890
EnsemblGeneIds (GRCh37): ENSG00000107890
OMIM: 610855, Gene2Phenotype
ANKRD26 is in 9 panels
EnsemblGeneIds (GRCh38): ENSG00000107890
EnsemblGeneIds (GRCh37): ENSG00000107890
OMIM: 610855, Gene2Phenotype
ANKRD26 is in 9 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert list
- Illumina TruGenome Clinical Sequencing Services
- Radboud University Medical Center, Nijmegen
- Phenotypes
-
- Thrombocytopenia 2, 188000
- Congenital amegkaryocytic thrombocytopenia
- OMIM
- 610855
- Clinvar variants
- Variants in ANKRD26
- Penetrance
- Complete
- Panels with this gene
-
- Haematological malignancies for rare disease
- Haematological malignancies cancer susceptibility
- Cytopenia - NOT Fanconi anaemia
- Inherited predisposition to acute myeloid leukaemia (AML)
- Bleeding and platelet disorders
- Cytopenias and congenital anaemias
- Inherited bleeding disorders
- Fetal anomalies
- DDG2P
History Filter Activity
22 Jul 2016, Gel status: 0
Created
Ellen McDonagh (Genomics England Curator)ANKRD26 was created by ellenmcdonagh
22 Jul 2016, Gel status: 2
Added New Source
Ellen McDonagh (Genomics England Curator)ANKRD26 was added to Anaemias and red cell disorderspanel. Sources: Radboud University Medical Center, Nijmegen,Illumina TruGenome Clinical Sequencing Services,Expert list