Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Ccer1 is a spermatid-specific gene required for spermatogenesis and male fertility

1 Jan 2024

Abstract excerpt

Male infertility is a multifactorial condition for which the underlying causes frequently remain undefined. Genetic factors have long been associated with male fertility. However, many of them are poorly or not at all characterized and their biological functions are unknown. Identifying the key genes behind male infertility is crucial for improving prognosis and treatment options, as well as for evaluating the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Share to Reproductive Biology and Fertility
Share to Sperm and Testicular Function

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 39868420
DOI: 10.1387/ijdb.240205rp

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Ccer1 is a spermatid-specific gene required for spermatogenesis and male fertilityPMID 39868420Read ↗

Ccdc87 is critical for sperm function and male fertility†Semantic proximity Read ↗

Disorders of spermatogenesisSemantic proximity Read ↗

A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse.Semantic proximity Read ↗

Coiled-coil domain-containing 38 is required for acrosome biogenesis and fibrous sheath assembly in miceSemantic proximity Read ↗

FertilityOnline, a straight pipeline for functional gene annotation and disease mutation discovery, identifies novel infertility causative mutations in <i>SYCE1</i> and <i>STAG3</i>Semantic proximity Read ↗

The control of male fertility by spermatid-specific factors: searching for contraceptive targets from spermatozoon’s head to tailSemantic proximity Read ↗

Drosophila Pif1A is essential for spermatogenesis and is the homolog of human CCDC157, a gene associated with idiopathic NOASemantic proximity Read ↗

Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice.Semantic proximity Read ↗

FertilityOnline: A Straightforward Pipeline for Functional Gene Annotation and Disease Mutation Discovery.Semantic proximity Read ↗

Male Infertility Diagnosis: Improvement of Genetic Analysis Performance by the Introduction of Pre-Diagnostic Genes in a Next-Generation Sequencing Custom-Made Panel.Semantic proximity Read ↗

Homozygous CCDC146 mutation causes oligoasthenoteratozoospermia in humans and mice.Semantic proximity Read ↗

CCDC89 is required for optimal sperm motility and male fertility in mammalsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.