Cytopenias and congenital anaemias
Gene: ARHGAP26EnsemblGeneIds (GRCh38): ENSG00000145819
EnsemblGeneIds (GRCh37): ENSG00000145819
OMIM: 605370, Gene2Phenotype
ARHGAP26 is in 1 panel
2 reviews
Ellen McDonagh (Genomics England Curator)
Comment on list classification: This gene is somatic only on the COSMIC Cancer Gene Census list, and not germline.Created: 22 Feb 2017, 4:30 p.m.
BRIDGE consortium (NIHRBR-RD)
Mode of inheritance
Unknown
Phenotypes
Myelodysplastic syndrome (MDS), Paediatric
Variants in this GENE are reported as part of current diagnostic practice
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Red
- BRIDGE consortium (NIHRBR-RD)
- Phenotypes
-
- Myelodysplastic syndrome (MDS), Paediatric
- Leukemia, juvenile myelomonocytic, somatic 607785
- Tags
- OMIM
- 605370
- Clinvar variants
- Variants in ARHGAP26
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
panel promoted to version 1
Arianna Tucci (Genomics England Curator)Promoted to V1 on 11 March 2017, after internal review and discussion with the clinical team.
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Set Phenotypes
Ellen McDonagh (Genomics England Curator)Phenotypes for ARHGAP26 were set to Myelodysplastic syndrome (MDS), Paediatric;Leukemia, juvenile myelomonocytic, somatic 607785
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Red List (Low Evidence).
Added New Source
Louise Daugherty (Genomics England Curator)ARHGAP26 was added to Cytopaenias and congenital anaemiaspanel. Sources: BRIDGE consortium (NIHRBR-RD)
Created
Louise Daugherty (Genomics England Curator)ARHGAP26 was created by LouiseD