HomeAboutRankingsData Sources
© 2026 GeneE
🧬
GeneE
10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
ⓘGeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
MEIOSIN
meiosis initiator
Chromosome 19 · 19q13.32
NCBI Gene: 388553Ensembl: ENSG00000237452.4HGNC: HGNC:44318UniProt: C9JSJ3
3PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transcription Factor
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
nucleusregulation of transcription by RNA polymerase IIspermatogenesisoogenesisSjogren syndromeazoospermiamyocardial infarctionpartial chromosome Y deletion
✦AI Summary

MEIOSIN is a DNA-binding transcriptional regulator that serves as the primary gatekeeper of meiotic initiation in both male and female germ cells 1. In complex with STRA8, MEIOSIN directly activates transcription of critical meiotic genes to orchestrate the cell-cycle switch from mitosis to meiosis 2. MEIOSIN operates downstream of retinoic acid signaling and acts at the G1/S phase transition to establish the meiotic prophase program, characterized by chromosome 19 and homolog synapsis 13. In spermatogenic cells, mRNA destabilization mediated by MEIOC-YTHDC2-RBM46 enhances cellular competence for MEIOSIN activation by derepressing meiosis-associated genes including Meiosin itself 4. Similarly, during oogenesis, MEIOC promotes meiotic entry by increasing MEIOSIN transcript abundance 5. Loss-of-function variants in MEIOSIN are associated with premature ovarian insufficiency (POI), a major cause of female infertility 6. Functionally, MEIOSIN missense variants can impair transcriptional activation of meiotic genes and disrupt nuclear localization through the HMG box domain, accelerating oocyte depletion 7. Additionally, MEIOSIN downregulation impairs spermatogenesis in response to environmental stressors 8. These findings establish MEIOSIN as essential for reproductive competence in both sexes.

Sources cited
1
MEIOSIN is a DNA-binding protein that directs meiotic initiation and meiotic prophase programs during spermatogenesis
PMID: 34955498
2
MEIOSIN and STRA8 initiate meiosis by activating meiotic genes and installing the meiotic prophase program
PMID: 38797021
3
MEIOSIN is responsive to retinoic acid and critical for meiosis
PMID: 34472453
4
MEIOC-mediated mRNA destabilization enhances competence for STRA8-MEIOSIN activation by derepressing Meiosin and other meiosis-associated genes
PMID: 38884383
5
MEIOC promotes meiotic entry by increasing Meiosin transcript abundance during mouse oogenesis
PMID: 41287933
6
MEIOSIN variants are associated with premature ovarian insufficiency and identified as POI-causative genes
PMID: 36732629
7
MEIOSIN missense variant impairs transcriptional activation of meiotic genes, disrupts nuclear localization, and accelerates oocyte depletion
PMID: 37982418
8
Meiosin gene downregulation impairs male reproductive function and spermatogenesis
PMID: 39804975
Disease Associationsⓘ20
Sjogren syndromeOpen Targets
0.08Suggestive
azoospermiaOpen Targets
0.08Suggestive
myocardial infarctionOpen Targets
0.07Suggestive
partial chromosome Y deletionOpen Targets
0.06Suggestive
perinatal diseaseOpen Targets
0.06Suggestive
coronary artery diseaseOpen Targets
0.06Suggestive
46,XX testicular disorder of sex developmentOpen Targets
0.05Suggestive
spermatogenic failure 25Open Targets
0.05Suggestive
spermatogenic failure 57Open Targets
0.05Suggestive
spermatogenic failure 50Open Targets
0.05Suggestive
spinocerebellar ataxia type 32Open Targets
0.05Suggestive
male infertility with azoospermia or oligozoospermia due to single gene mutationOpen Targets
0.05Suggestive
isochromosomy YpOpen Targets
0.05Suggestive
Isolated follicle stimulating hormone deficiencyOpen Targets
0.05Suggestive
spermatogenic failure, X-linked, 2Open Targets
0.05Suggestive
asthmaOpen Targets
0.05Suggestive
spermatogenic failure 71Open Targets
0.05Suggestive
spermatogenic failure 63Open Targets
0.05Suggestive
partial androgen insensitivity syndromeOpen Targets
0.05Suggestive
congenital bilateral absence of vas deferensOpen Targets
0.05Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
STRA8Shared pathway72%ZNF35Shared pathway50%REC114Shared pathway40%HORMAD1Shared pathway38%MEIOCCo-mentioned in literature38%DUSP13BShared pathway29%
Tissue Expression6 tissues
Heart
0%
Lung
0%
Brain
0%
Bone Marrow
0%
Ovary
0%
Liver
0%
Gene Interaction Network
Click a node to explore
MEIOSINSTRA8ZNF35REC114HORMAD1MEIOCDUSP13B
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt C9JSJ3
View on AlphaFold ↗
RankingsWhere MEIOSIN stands among ~20K protein-coding genes
  • #18,906of 20,598
    Most Researched3
Genes detectedMEIOSIN
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Mechanisms of meiosis initiation and meiotic prophase progression during spermatogenesis.
PMID: 38797021
Mol Aspects Med · 2024
1.00
2
Landscape of pathogenic mutations in premature ovarian insufficiency.
PMID: 36732629
Nat Med · 2023
0.90
3
MEIOSIN directs initiation of meiosis and subsequent meiotic prophase program during spermatogenesis.
PMID: 34955498
Genes Genet Syst · 2022
0.80
4
Destabilization of mRNAs enhances competence to initiate meiosis in mouse spermatogenic cells.
PMID: 38884383
Development · 2024
0.70
5
MEIOC prevents continued mitotic cycling and promotes meiotic entry during mouse oogenesis.
PMID: 41287933
Development · 2026
0.60