Gene
SRSF2
serine and arginine rich splicing factor 2
- HGNC 10783↗(opens in a new tab)
- Ensembl gene ENSG00000161547↗(opens in a new tab)
- NCBI Gene 6427↗(opens in a new tab)
Summary
- Cytogenetic location
- 17q25.2
- Coordinates
- Chromosome 17: 76,734,115–76,737,331 (GRCh38)
- Exons
- 3 exons across 3.2 kb
- Protein
- 221 amino acids
- Also known as
- SC-35, SC35, PR264, SFRS2A
- Previous symbols
- SFRS2
- MANE Select transcript
- ENST00000359995.10NM_001195427.2
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read SRSF2, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads SRSF2 yet. The test sequences your whole genome, so your data includes it all the same.
How SRSF2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 1.9 kb of the gene's 3.2 kb; 666 of those bases code for the protein.
Traits linked to SRSF2
The Human Phenotype Ontology lists these as features of the rare conditions SRSF2 can cause. Each trait's page lists the other genes linked to it.
Abnormality of blood and blood-forming tissues
- Abnormal mast cell morphology
- Blood tumor
- Myeloid leukemia
- Bone marrow hypercellularity
- Elevated white blood count
- High blood eosinophil count
- Increased CD25+ mast cell proportion
- Low platelet count
Show 17 more traits
- Myeloproliferative disorder
- Normochromic anemia
- Normocytic anemia
- Acute myeloid leukemia
- Blood cancer
- Cancer of lymphatic system
- Chronic myelomonocytic leukemia
- Gastrointestinal bleeding
- Granulocytic hyperplasia
- Increased blood neutrophil counts
- Increased total basophil count
- Low blood cell count
- Low blood neutrophil count
- Low number of red blood cells or hemoglobin
- Myelodysplasia
- Chronic lymphatic leukemia
- Multiple myeloma
Abnormality of the digestive system
- Abdominal cramps
- Abdominal pain
- Anorexia
- Diarrhea
- Malabsorption
- Accumulation of fluid in the abdomen
- Decreased liver function
- Enlarged liver
Show 2 more traits
Abnormality of the cardiovascular system
- Enlarged liver and spleen
- Low blood pressure
- Swollen lymph nodes
- Elevated heart rate
- Fainting spell
- Hives
- Hypersplenism
- Increased spleen size
Show 1 more trait
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
Cite this page
Dante Labs. (n.d.). SRSF2 gene: serine and arginine rich splicing factor 2. Retrieved 17 October 2026, from https://dantelabs.com/genes/srsf2
Dante Labs. SRSF2 gene: serine and arginine rich splicing factor 2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/srsf2
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks