Varaico: Literature-Extracted Genetic Variants

Gene:ZP2
Variant:p.G565Splc
Back to variants list

ZP2

NM_001376232.1:p.G565Splc

Associated Papers

Advances in monogenic female infertility.

Gu H et al.

Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2025

Defects in mRNA splicing and implications for infertility: a comprehensive review and in silico analysis.

Li K et al.

Human Reproduction Update, 2025

A Compound Heterozygous Pathogenic Variant in ZP2 Gene Causes Female Infertility.

Yang S et al.

Reproductive Sciences (thousand Oaks, Calif.), 2025

Identification of zona pellucida defects revealed a novel loss-of-function mutation in ZP2 in humans and rats.

Zeng J et al.

Frontiers in Endocrinology, 2023

Can successful pregnancy be achieved and predicted from patients with identified ZP mutations? A literature review.

Zhou J et al.

Reproductive Biology and Endocrinology : Rb&e, 2022

Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility.

Hou M et al.

Reproductive Sciences (thousand Oaks, Calif.), 2022

Novel mutations in ZP2 and ZP3 cause female infertility in three patients.

Jia W et al.

Journal of Assisted Reproduction and Genetics, 2022

Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and mice.

Shen Y et al.

Human Reproduction (oxford, England), 2022

Gene Spectrum and Clinical Traits of Nine Patients With Oocyte Maturation Arrest.

Huo M et al.

Frontiers in Genetics, 2022

Gene mutations associated with fertilization failure after in vitro fertilization/intracytoplasmic sperm injection.

Xue Y et al.

Frontiers in Endocrinology, 2022

A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility.

Sun Y et al.

Journal of Assisted Reproduction and Genetics, 2021

Human Zona Pellucida Glycoproteins: Binding Characteristics With Human Spermatozoa and Induction of Acrosome Reaction.

Gupta SK

Frontiers in Cell and Developmental Biology, 2021

Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida.

Luo G et al.

Journal of Assisted Reproduction and Genetics, 2020

Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human.

Cao Q et al.

Journal of Cellular and Molecular Medicine, 2020

Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation.

Zhou Z et al.

Human Genetics, 2019

ZP2 pathogenic variants cause in vitro fertilization failure and female infertility.

Dai C et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019

[The human zona pellucida: New genetic findings].

Trocka D et al.

Medecine Sciences : M/s, 0

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."