Annotation Detail
Information
- Associated Genes
- RUNX1T1
- Associated Variants
-
RUNX1T1 MUTATION
RUNX1T1 MUTATION - Associated Disease
- Neoplasm, Residual
- Source Database
- DisGeNET
- Description
- We asked whether minimal residual disease (MRD) determined by RUNX1/RUNX1T1 transcript levels could identify allogeneic hematopoietic stem cell transplantation (allo- HSCT) t(8;21) (q22;q22) acute myeloid leukemia patients who are at high risk for relapse, together with the impact of c-KIT mutations.
- Pubmed
- 25082877
- Section of the abstract supporting the evidence
- ALL_TEXT_1/3
- Number of the section of the abstract supporting the evidence
- 1
- Number of the sentence supporting the evidence
- 1
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.00651460492992728
Drugs