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Widening the Spectrum of Fusion Events in Schwannoma: Identification of a Novel TANC1::HTRA1 Fusion

delete2025-08-07
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PRE
AI
J
James Watkins *
P
Patrick Tarpey
M
Maria O’Donovan
J
John A. Tadross
N
N. Mohammed
DOI:10.1002/gcc.70072delete
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Abstract

Abstract

En 中文
A range of genomic drivers have been identified in schwannomas, including a number of translocations, most commonly SH3PXD2A::HTRA1. To date, despite the analysis of large numbers of cases, no examples of variant HTRA1 partners have been described. We describe a schwannoma arising in the periportal region in which a novel TANC1::HTRA1 fusion was identified. The identification of this variant expands the range of fusion drivers in schwannoma and offers insight into the pathogenic mechanism of HTRA1 fusions and their utility in molecular diagnosis.

Journal

Genes Chromosomes and Cancer cover
Genes Chromosomes and Cancer
IF:
2.8
Papers:
3.3K
Citations:
4.7K

Organization

C
Cambridge University Hospitals NHS Foundation Trust
Scholars:
8.1K
Papers: 5.5K
Citations: 4.9K
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