Varaico: Literature-Extracted Genetic Variants

Gene:MEIOB
Variant:p.S366delFs
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MEIOB

NM_001163560.3:p.S366delFs

Associated Papers

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

Genetic determinants of testicular sperm extraction outcomes: insights from a large multicentre study of men with non-obstructive azoospermia.

Riera-Escamilla A et al.

Human Reproduction Open, 2025

40896145 (PubMed )
Supplement: hoaf049_supplementary_data.zip › HRO-25-0045-R2-SuppTablesS2-S4_and_S6-S9.xlsx › ST6

Screening by single-molecule molecular inversion probes targeted sequencing panel of candidate genes of infertility in azoospermic infertile Jordanian males.

Batiha O et al.

Human Fertility (cambridge, England), 2022

Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia.

Wang Y et al.

Frontiers in Genetics, 2022

Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB.

Wu Y et al.

Human Reproduction (oxford, England), 2021

Shared genetics between nonobstructive azoospermia and primary ovarian insufficiency.

Verrilli L et al.

F&s Reviews, 2021

A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest.

Gershoni M et al.

Human Reproduction (oxford, England), 2019

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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."