SOX7
Overview
SOX7 encodes a member of the SOX (SRY-box) family of transcription factors involved in developmental regulation of vascular endothelium and hematopoiesis. Located at 8p23.1, SOX7 is subject to co-deletion with other genes in this region in multiple myeloma and other cancers; its tumor-suppressive role in hematologic malignancies is under investigation.
Alterations observed in the corpus
- Co-deleted within the 8p23.1 homozygous-deletion peak (18 genes) in multiple myeloma; MM relevance not previously established at the time of reporting PMID:24434212
Cancer types (linked)
- MM: co-deleted within the 8p23.1 homozygous-deletion peak in a comprehensive MM genomic analysis PMID:24434212
Co-occurrence and mutual exclusivity
- Co-deleted with BLK, MSRA, and PINX1 within the 8p23.1 deletion peak in multiple myeloma PMID:24434212
Therapeutic relevance
- No direct therapeutic targeting reported in this corpus.
Open questions
- Functional role of SOX7 co-deletion in MM pathogenesis is not established; driver versus passenger status at this locus is unclear.
Sources
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