Indicator Explainer
ARID1B Gene
This gene plays a role in both chromatin remodeling and transcriptional regulation.
This page explains what the indicator is and how results are interpreted in general terms. Reference ranges depend on the laboratory, the method, and your own situation — no single “normal value” applies to everyone. This page is health information, not a diagnosis. For symptoms, treatment, or urgent concerns, contact a healthcare professional.
When it is tested
Source: National Cancer Institute, NCI Thesaurus 26.09d, C102520. NCI definition, reproduced without modification under CC BY 4.0. Source identity and definition checked automatically on 2026-10-20. No individual clinical interpretation or human reviewer is asserted.
Reading results
Reference intervals and interpretation depend on the laboratory, specimen, method and clinical context. This source definition is educational information; it does not establish a diagnosis, product approval or suitability for an individual.
Also Known As
References
- NCI Thesaurus 26.09d — ARID1B Gene (C102520)
- Source: National Cancer Institute, NCI Thesaurus 26.09d, C102520. NCI definition, reproduced without modification under CC BY 4.0.
- Infantile giant intracranial-extracranial communicating mixed germ cell tumor with ARID1B gene mutation: a case report. — Front Oncol, 2026-07-22 (PMID 42558373; literature)
- Identification of novel variants in the ARID1B gene causing Coffin-Siris syndrome. — Eur J Pediatr, 2026-01-17 (PMID 41545737; literature)
- Long-Read Sequencing of a Neurodevelopmental Disorder Patient Reveals Complex Rearrangement Involving the ARID1B Gene. — Am J Med Genet A, 2025-09-11 (PMID 40931928; literature)
- [ARID1B Gene Deletion Promotes the Proliferation, Migration and Invasion of NSCLC Cells]. — Zhongguo Fei Ai Za Zhi, 2025-03-01 (PMID 40210476; literature)
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia. — BMC Med Genomics, 2024-05-24 (PMID 38790056; literature)
- [Genetic analysis of two children with Coffin-Siris syndrome due to variants of ARID1B gene]. — Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2024-01-01 (PMID 38171562; literature)