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srsf2
SRSF2
SRSF2 encodes a spliceosome serine-arginine protein; P95H hotspot alters CCNG exonic splicing enhancer recognition → aberrant mRNA splicing; SRSF2 P95H mutations occur in ~45% of CMML (with TET2 co-mutation), ~15% of MDS, and ~11% of PTCL; no direct targeted therapy.
Entry Metadata
| Field | Value |
|---|---|
| ID | srsf2 |
| Name | SRSF2 |
| Status | draft |
| Last reviewed | 2026-06-06 |
| Atlas | 01-human |
| Scale | 03-molecular |
Cross-Atlas Connections
Sources
- Yoshida K, Sanada M, Shiraishi Y, et al. Frequent pathway mutations of splicing machinery in myeloid diseases. Nature. 2011;478(7367):64-69. · PubMed 21909114
- Patnaik MM, Lasho TL, Finke CM, et al. Spliceosome mutations involving SRSF2, SF3B1, and U2AF35 in chronic myelomonocytic leukemia: prevalence, clinical correlates, and prognostic relevance. Am J Hematol. 2013;88(3):201-206. · PubMed 23335075