Cytopenias and congenital anaemias
Gene: ZRSR2EnsemblGeneIds (GRCh38): ENSG00000169249
EnsemblGeneIds (GRCh37): ENSG00000169249
OMIM: 300028, Gene2Phenotype
ZRSR2 is in 2 panels
2 reviews
Rebecca Foulger (Genomics England curator)
Comment on list classification: Kept rating as red because COSMIC and literature (e.g. PMID:27543316, PMID:25550361) support somatic variants as causative for AML.Created: 9 Mar 2017, 3:30 p.m.
Somatic variants only, reported in COSMIC cancer gene census.Created: 9 Mar 2017, 3:18 p.m.
BRIDGE consortium (NIHRBR-RD)
Mode of inheritance
Unknown
Phenotypes
Acute myeloid leukaemia (AML); Chronic Myeloid Leukemia (CML)
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
-
- Acute myeloid leukaemia (AML)
- Chronic Myeloid Leukemia (CML)
- Tags
- OMIM
- 300028
- Clinvar variants
- Variants in ZRSR2
- Penetrance
- Complete
- Publications
- 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
Rebecca Foulger (Genomics England curator)This gene has been classified as Red List (Low Evidence).
Set publications
Rebecca Foulger (Genomics England curator)Publications for ZRSR2 were set to 25550361; 27543316; 22389253
Created
Louise Daugherty (Genomics England Curator)ZRSR2 was created by LouiseD
Added New Source
Louise Daugherty (Genomics England Curator)ZRSR2 was added to Cytopaenias and congenital anaemiaspanel. Sources: BRIDGE consortium (NIHRBR-RD)