Association of single nucleotide polymorphism c.673C>A/p.Gln225Lys in SEPT12 gene with spermatogenesis failure in male idiopathic infertility in Northeast China

D Geng, X Yang, H Zhang, X Liu, Y Yu… - Journal of …, 2019 - journals.sagepub.com
Male infertility is a complex multifactorial disease affecting approximately 10% of couples
who want to have children. Some cases of infertility can be explained by genetic factors …

[HTML][HTML] New single nucleotide polymorphism G5508A in the SEPT12 gene may be associated with idiopathic male infertility in Iranian men

M Shahhoseini, M Azad, M Sabbaghian… - Iranian Journal of …, 2015 - ncbi.nlm.nih.gov
Background: Male infertility is a multifactorial disorder, which affects approximately 10% of
couples at childbearing age with substantial clinical and social impact. Genetic factors are …

Single‐nucleotide polymorphism c.474G>A in the SEPT12 gene is a predisposing factor in male infertility

A Rafaee, A Mohseni Meybodi… - Molecular …, 2020 - Wiley Online Library
SEPT12 is a testis‐specific gene involved in the terminal differentiation of male germ cells.
SEPT12 protein is required for sperm head‐tail formation and acts as a fundamental …

SEPTIN12 Genetic Variants Confer Susceptibility to Teratozoospermia

YH Lin, YY Wang, HI Chen, YC Kuo, YW Chiou… - PLoS …, 2012 - journals.plos.org
It is estimated that 10–15% of couples are infertile and male factors account for about half of
these cases. With the advent of intracytoplasmic sperm injection (ICSI), many infertile men …

Single‐Nucleotide Polymorphisms in the SEPTIN12 Gene May Be a Genetic Risk Factor for Japanese Patients With Sertoli Cell–Only Syndrome

H Miyakawa, T Miyamoto, E Koh… - Journal of …, 2012 - Wiley Online Library
Genetic mechanisms have been implicated as a cause of some cases of male infertility.
Recently, 10 novel genes involved in human spermatogenesis, including human SEPTIN12 …

SEPTIN12 c. 474 G> A polymorphism as a risk factor in teratozoospermic patients

G Özkara, N Ersoy Tunali - Molecular biology reports, 2021 - Springer
Teratozoospermia is a condition related to poor morphologically normal sperm count below
the lower reference limit, which could hinder natural conception. Single nucleotide …

A novel SEPT12 mutation, T96I, is associated with sperm head and annulus defects

KR Chen, HY Wang, YC Kuo, YC Lo… - Frontiers in Cell and …, 2025 - frontiersin.org
Infertility affects around 8%–12% of reproductive-aged couples and is a major health
concern. Both genetic and environmental factors influence male infertility. SEPTIN12 is a …

SEPT12 mutations cause male infertility with defective sperm annulus

YC Kuo, YH Lin, HI Chen, YY Wang, YW Chiou… - Human …, 2012 - Wiley Online Library
Septins are members of the GTPase superfamily, which has been implicated in diverse
cellular functions including cytokinesis and morphogenesis. Septin 12 (SEPT12) is a testis …

Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men

T Miyamoto, A Tsujimura, Y Miyagawa, E Koh… - Journal of assisted …, 2012 - Springer
Purpose To investigate the association between SEPTIN12 gene variants and the risk of
azoospermia caused by meiotic arrest. Methods Mutational analysis of the SEPTIN12 gene …

Homozygous Loss of Septin12, but not its Haploinsufficiency, Leads to Male Infertility and Fertilization Failure

H Chen, P Li, X Du, Y Zhao, L Wang, Y Tian… - Frontiers in Cell and …, 2022 - frontiersin.org
The SEPTIN12 gene has been associated with male infertility. Male Septin12+/− chimera
mice were infertile, supporting the prevailing view that SEPTIN12 haploinsufficiency causes …