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GeneE
8 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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MEIOC
meiosis specific with coiled-coil domain
Chromosome 17 · 17q21.31
NCBI Gene: 284071Ensembl: ENSG00000180336.19HGNC: HGNC:26670UniProt: A2RUB1
17PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Highly Constrained
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
male meiosis Igermline cell cycle switching, mitotic to meiotic cell cyclechromosome organization involved in meiotic cell cyclenucleuspreeclampsiaazoospermiaobesitypartial chromosome Y deletion
✦AI Summary

MEIOC (meiosis specific with coiled-coil domain) is an RNA-binding protein essential for meiosis completion in both male and female germ cells. Its primary function is to stabilize meiotic mRNAs while simultaneously destabilizing mitotic transcripts, enabling the critical transition from mitotic to meiotic cell cycle programs 1. MEIOC operates as part of a posttranscriptional regulatory complex with RNA helicase YTHDC2 and RNA-binding protein RBM46, which together target mitotic genes like E2f6 and Mga for degradation 23. This mRNA decay mechanism derepresses meiosis-associated genes, including Meiosin, thereby conferring molecular competence for meiotic entry 3. In oogenesis, MEIOC additionally prevents continued mitotic cycling by downregulating the G1/S cyclin CCNA2, while promoting entry into meiosis via the STRA8-MEIOSIN pathway 4. Importantly, MEIOC's function operates independently of retinoic acid signaling, suggesting it represents an ancestral posttranscriptional mechanism complementing transcriptional regulation 1. Dysfunction of MEIOC or its binding partners causes early meiotic defects and infertility in mice, with dysregulated expression associated with human male fertility disorders 2. MEIOC overexpression promotes meiotic initiation from human pluripotent stem cells, indicating therapeutic potential for infertility treatment 56.

Sources cited
1
MEIOC prevents meiotic transcript degradation and is required for meiosis implementation in males and females; functions independently of retinoic acid signaling
PMID: 26742488
2
MEIOC and YTHDC2 form essential posttranscriptional regulatory complex; RBM46 targets mitotic transcripts for degradation; dysregulated expression associated with human male fertility disorders
PMID: 36001654
3
MEIOC-YTHDC2-RBM46 complex destabilizes mitotic genes E2f6 and Mga to derepress meiosis-associated genes and enhance meiotic competence before meiotic initiation
PMID: 38884383
4
MEIOC prevents mitotic cycling by downregulating CCNA2 and promotes meiotic entry by increasing Meiosin transcript abundance in oogenic cells
PMID: 41287933
5
MEIOC overexpression rapidly activates meiosis from human iPSCs under defined conditions, generating cells expressing meiotic markers and synaptonemal complex components
PMID: 40815662
6
MEIOC overexpression induces human meiosis with progressive stages (leptonema, zygonema, pachynema) and chromosome synapsis in pluripotent stem cells
PMID: 38854076
Disease Associationsⓘ20
preeclampsiaOpen Targets
0.24Weak
azoospermiaOpen Targets
0.08Suggestive
obesityOpen Targets
0.07Suggestive
partial chromosome Y deletionOpen Targets
0.07Suggestive
primary ovarian insufficiencyOpen Targets
0.06Suggestive
spinocerebellar ataxia type 32Open Targets
0.06Suggestive
isochromosomy YpOpen Targets
0.05Suggestive
spermatogenic failure 25Open Targets
0.05Suggestive
spermatogenic failure 50Open Targets
0.05Suggestive
spermatogenic failure 57Open Targets
0.05Suggestive
Isolated follicle stimulating hormone deficiencyOpen Targets
0.05Suggestive
spermatogenic failure 71Open Targets
0.05Suggestive
congenital bilateral absence of vas deferensOpen Targets
0.05Suggestive
partial androgen insensitivity syndromeOpen Targets
0.05Suggestive
spermatogenic failure, X-linked, 2Open Targets
0.05Suggestive
isochromosomy YqOpen Targets
0.05Suggestive
spermatogenic failure 63Open Targets
0.05Suggestive
46,XX testicular disorder of sex developmentOpen Targets
0.05Suggestive
spermatogenic failure 48Open Targets
0.05Suggestive
spermatogenic failure 12Open Targets
0.05Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
YTHDC2Protein interaction97%MEIOSINCo-mentioned in literature38%HSF2BPShared pathway25%RBM46Co-mentioned in literature25%DMC1Shared pathway22%HORMAD1Shared pathway21%
Tissue Expression6 tissues
Brain
100%
Bone Marrow
65%
Liver
35%
Lung
24%
Ovary
24%
Heart
21%
Gene Interaction Network
Click a node to explore
MEIOCYTHDC2MEIOSINHSF2BPRBM46DMC1HORMAD1
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt A2RUB1
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.22Highly Constrained
pLIⓘ
1.00Intolerant
Observed/Expected LoF0.13 [0.07–0.22]
RankingsWhere MEIOC stands among ~20K protein-coding genes
  • #15,053of 20,598
    Most Researched17
  • #559of 17,882
    Most Constrained (LOEUF)0.22 · top 5%
Genes detectedMEIOC
Sources retrieved8 papers
Response time—
📄 Sources
8▼
1
RNA binding protein RBM46 regulates mitotic-to-meiotic transition in spermatogenesis.
PMID: 36001654
Sci Adv · 2022
1.00
2
Destabilization of mRNAs enhances competence to initiate meiosis in mouse spermatogenic cells.
PMID: 38884383
Development · 2024
0.88
3
MEIOC prevents continued mitotic cycling and promotes meiotic entry during mouse oogenesis.
PMID: 41287933
Development · 2026
0.75
4
Initiation of meiosis from human iPSCs under defined conditions through identification of regulatory factors.
PMID: 40815662
Sci Adv · 2025
0.63
5
Implementation of meiosis prophase I programme requires a conserved retinoid-independent stabilizer of meiotic transcripts.
PMID: 26742488
Nat Commun · 2016
0.50