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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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MNDA
myeloid cell nuclear differentiation antigen
Chromosome 1 · 1q23.1
NCBI Gene: 4332Ensembl: ENSG00000163563.9HGNC: HGNC:7183UniProt: P41218
46PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transcription Factor
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
nucleoplasmnucleoluscytosolextracellular exosomeCOVID-19type 1 diabetes mellitusThrombocytopeniaautosomal dominant macrothrombocytopenia
✦AI Summary

MNDA (myeloid cell nuclear differentiation antigen) is a PYHIN family protein that functions as a transcriptional regulator in leukocytes, playing critical roles in immune responses and cell death control 1. In myeloid cells, MNDA acts as a transcriptional activator/repressor during granulocyte and monocyte responses to interferon, while also regulating B cell functions through negative regulation of proliferation and involvement in B cell receptor signaling 1. Mechanistically, MNDA localizes primarily to the nucleus of myeloid and lymphoid leukocytes and directly controls transcription of genes encoding factors that regulate apoptosis and inflammation 1. Its subcellular localization is dynamically modulated in response to genotoxic agents and bacterial constituents, allowing rapid cellular responses to stress and infection 1. Clinically, MNDA expression abnormalities have significant implications for hematopoietic diseases characterized by defective apoptosis regulation, where MNDA serves as both a lymphoma marker and prognostic factor 1. Abnormal MNDA expression associates with altered cytokine and inflammatory mediator levels, suggesting its involvement in dysregulated immune responses 1. Understanding MNDA's regulatory mechanisms and molecular functions could substantially influence management and treatment strategies for hematologic and inflammatory diseases.

Sources cited
1
MNDA is a PYHIN protein involved in transcriptional regulation of apoptosis and inflammation genes in leukocytes; functions as transcriptional activator/repressor; nuclear localization modulated by genotoxic agents and bacterial constituents; clinical relevance as lymphoma marker and prognostic factor for hematopoietic diseases
PMID: 38680493
⚠Limited data available — This gene has 1 indexed publication. Summary and analysis may be incomplete.
Disease Associationsⓘ20
COVID-19Open Targets
0.30Weak
type 1 diabetes mellitusOpen Targets
0.23Weak
ThrombocytopeniaOpen Targets
0.06Suggestive
autosomal dominant macrothrombocytopeniaOpen Targets
0.05Suggestive
ovarian carcinomaOpen Targets
0.05Suggestive
macrothrombocytopenia, isolated, 2, autosomal dominantOpen Targets
0.05Suggestive
thrombocytopenia 4Open Targets
0.05Suggestive
spondylolisthesisOpen Targets
0.04Suggestive
osteosarcomaOpen Targets
0.04Suggestive
congenital amegakaryocytic thrombocytopenia 1Open Targets
0.04Suggestive
thrombocytopenia 7Open Targets
0.04Suggestive
hyper-IgE recurrent infection syndrome 5, autosomal recessiveOpen Targets
0.04Suggestive
Beta-thalassemia - X-linked thrombocytopeniaOpen Targets
0.04Suggestive
beta-thalassemia-X-linked thrombocytopenia syndromeOpen Targets
0.04Suggestive
platelet-type bleeding disorder 9Open Targets
0.04Suggestive
platelet-type bleeding disorder 15Open Targets
0.04Suggestive
X-linked sideroblastic anemia 1Open Targets
0.04Suggestive
autoimmune thrombocytopenic purpuraOpen Targets
0.04Suggestive
thrombocytopenia 2Open Targets
0.04Suggestive
monosomy 7 myelodysplasia and leukemia syndrome 1Open Targets
0.03Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
FCGR3BProtein interaction95%TYROBPProtein interaction93%CD53Protein interaction92%FCGR3AProtein interaction92%FGRProtein interaction92%HCKProtein interaction92%
Tissue Expression6 tissues
Bone Marrow
100%
Lung
30%
Heart
4%
Liver
4%
Brain
3%
Ovary
1%
Gene Interaction Network
Click a node to explore
MNDAFCGR3BTYROBPCD53FCGR3AFGRHCK
PROTEIN STRUCTURE
Preparing viewer…
PDB5H7Q · 1.45 Å · X-ray
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
1.56LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF1.20 [0.93–1.56]
RankingsWhere MNDA stands among ~20K protein-coding genes
  • #9,347of 20,598
    Most Researched46
  • #15,464of 17,882
    Most Constrained (LOEUF)1.56
Genes detectedMNDA
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Amyotrophic Lateral Sclerosis.
PMID: 28700839
N Engl J Med · 2017
1.00
2
Amyotrophic lateral sclerosis.
PMID: 28552366
Lancet · 2017
0.90
3
C9orf72-mediated ALS and FTD: multiple pathways to disease.
PMID: 30120348
Nat Rev Neurol · 2018
0.80
4
A proposal for new diagnostic criteria for ALS.
PMID: 32387049
Clin Neurophysiol · 2020
0.70
5
Supportive and symptomatic management of amyotrophic lateral sclerosis.
PMID: 27514291
Nat Rev Neurol · 2016
0.60