Varaico: Literature-Extracted Genetic Variants

Gene:ARHGAP35
Variant:p.S866F
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ARHGAP35

NM_004491.5:p.S866F

Associated Papers

Integrating evidence from protein domains to identify cancer driver mutations.

Ostroverkhova D et al.

Protein Science : a Publication of the Protein Society, 2026

41556616 (PubMed )
Supplement: PRO-35-e70422-s002.xlsx › Table_S1

Establishment and validation of a phenotype-driven predictive model for the diagnostic efficacy of trio-based whole exome sequencing (trio-WES) in children with genetic neurodevelopmental disorders (g-NDDs).

Wu R et al.

Frontiers in Neurology, 2025

41170324 (PubMed )
Supplement: Data_Sheet_5.XLS › NDD-NPDs

Tumor-derived ARHGAP35 mutations enhance the Gα13-Rho signaling axis in human endometrial cancer.

Yagi H et al.

Cancer Gene Therapy, 2023

Identification of an inhibitory domain in GTPase-activating protein p190RhoGAP responsible for masking its functional GAP domain.

Héraud C et al.

The Journal of Biological Chemistry, 2023

Mutational drivers of cancer cell migration and invasion.

Novikov NM et al.

British Journal of Cancer, 2021

p190A inactivating mutations cause aberrant RhoA activation and promote malignant transformation via the Hippo-YAP pathway in endometrial cancer.

Wen X et al.

Signal Transduction and Targeted Therapy, 2020

p190RhoGAPs, the ARHGAP35- and ARHGAP5-Encoded Proteins, in Health and Disease.

Héraud C et al.

Cells, 2019

Cancer-associated mutations in the protrusion-targeting region of p190RhoGAP impact tumor cell migration.

Binamé F et al.

The Journal of Cell Biology, 2016

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."