Cortney Gensemer, PhD on Instagram: “What is tenascin x (TNXB)? This might be the gene I am asked about the most. Many people wonder if their EDS could be caused by TNXB,
![Rare neurological manifestations in a Saudi Arabian patient with Ehlers–Danlos syndrome and a novel homozygous variant in the TNXB gene - Al‐Harbi - 2022 - American Journal of Medical Genetics Part A - Rare neurological manifestations in a Saudi Arabian patient with Ehlers–Danlos syndrome and a novel homozygous variant in the TNXB gene - Al‐Harbi - 2022 - American Journal of Medical Genetics Part A -](https://onlinelibrary.wiley.com/cms/asset/7574ae42-7eb9-4090-900d-af741cfc9f09/ajmga62539-fig-0001-m.jpg)
Rare neurological manifestations in a Saudi Arabian patient with Ehlers–Danlos syndrome and a novel homozygous variant in the TNXB gene - Al‐Harbi - 2022 - American Journal of Medical Genetics Part A -
![A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia - Lao - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia - Lao - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/7ef585b4-2e0e-4e5f-848c-7c829c1dd75f/mgg31556-fig-0001-m.jpg)
A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia - Lao - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
![Salt-wasting congenital adrenal hyperplasia phenotype as a result of the TNXA/TNXB chimera 1 (CAH-X CH-1) and the pathogenic IVS2-13A/C > G in CYP21A2 gene | SpringerLink Salt-wasting congenital adrenal hyperplasia phenotype as a result of the TNXA/TNXB chimera 1 (CAH-X CH-1) and the pathogenic IVS2-13A/C > G in CYP21A2 gene | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs42000-022-00410-w/MediaObjects/42000_2022_410_Fig2_HTML.png)
Salt-wasting congenital adrenal hyperplasia phenotype as a result of the TNXA/TNXB chimera 1 (CAH-X CH-1) and the pathogenic IVS2-13A/C > G in CYP21A2 gene | SpringerLink
![Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene | Journal of Medical Genetics Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/40/5/e53/F1.large.jpg)
Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene | Journal of Medical Genetics
![Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome](https://www.mdpi.com/genes/genes-10-00967/article_deploy/html/images/genes-10-00967-g001.png)
Genes | Free Full-Text | Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome
![PDF] Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia. | Semantic Scholar PDF] Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a8797a51b155ea54bcbbd3ab1cdfabe78e6d2fe9/6-Figure2-1.png)
PDF] Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia. | Semantic Scholar
![Missense mutations in TNXB as a cause of VUR. (A) Exons and protein... | Download Scientific Diagram Missense mutations in TNXB as a cause of VUR. (A) Exons and protein... | Download Scientific Diagram](https://www.researchgate.net/publication/236339440/figure/fig4/AS:668497902305283@1536393728638/Missense-mutations-in-TNXB-as-a-cause-of-VUR-A-Exons-and-protein-domains-of-TNXB-B.png)
Missense mutations in TNXB as a cause of VUR. (A) Exons and protein... | Download Scientific Diagram
![Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients - Demirdas - 2017 - Clinical Genetics - Wiley Online Library Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients - Demirdas - 2017 - Clinical Genetics - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/c9f61b8c-9866-445e-a755-d6401bb82cb0/cge12853-toc-0001-m.jpg?trick=1681668896101)
Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients - Demirdas - 2017 - Clinical Genetics - Wiley Online Library
![Mutation analysis of the TNXB gene in CAH-X patients. A, Schematic of... | Download Scientific Diagram Mutation analysis of the TNXB gene in CAH-X patients. A, Schematic of... | Download Scientific Diagram](https://www.researchgate.net/publication/234043450/figure/fig1/AS:299973414539270@1448530643499/Mutation-analysis-of-the-TNXB-gene-in-CAH-X-patients-A-Schematic-of-the-tenascin-genes.png)