Varaico: Literature-Extracted Genetic Variants

Gene:TEX11
Variant:p.M171V
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TEX11

NM_001003811.2:p.M171V

Associated Papers

Tex11 Mutant Mouse Models of Human Azoospermia.

Atkins GR et al.

Biorxiv : the Preprint Server for Biology, 2026

Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencing.

Ibrahim R et al.

Reproductive Biology, 2025

Incidental and secondary findings in trio exome sequencing.

Cohen C et al.

Genes & Diseases, 2024

38523675 (PubMed )
Supplement: mmc3.pdf

Genetic control of meiosis surveillance mechanisms in mammals.

Huang Y et al.

Frontiers in Cell and Developmental Biology, 2023

36910159 (PubMed )
Supplement: DataSheet2.PDF

Novel mutations of TEX11 are associated with non-obstructive azoospermia.

Song J et al.

Frontiers in Endocrinology, 2023

Correction: Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.

Tang D et al.

Reproductive Biology and Endocrinology : Rb&e, 2022

Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.

Tang D et al.

Reproductive Biology and Endocrinology : Rb&e, 2022

Targeted next-generation sequencing panel screening of 668 Chinese patients with non-obstructive azoospermia.

An M et al.

Journal of Assisted Reproduction and Genetics, 2021

Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes.

Chen S et al.

Human Molecular Genetics, 2020

Genetic defects in human azoospermia.

Ghieh F et al.

Basic and Clinical Andrology, 2019

A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.

Sha Y et al.

Bmc Medical Genetics, 2018

Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations.

Nakamura S et al.

Andrology, 2017

TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.

Yang F et al.

Embo Molecular Medicine, 2015

X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.

Yatsenko AN et al.

The New England Journal of Medicine, 2015

A new TEX11 mutation causes azoospermia and testicular meiotic arrest.

Yu XC et al.

Asian Journal of Andrology, 0

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