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GeneE
10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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THSD7A
thrombospondin type 1 domain containing 7A
Chromosome 7 · 7p21.3
NCBI Gene: 221981Ensembl: ENSG00000005108.17HGNC: HGNC:22207UniProt: Q9UPZ6
46PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingplasma membraneactin cytoskeleton organizationextracellular regionglaucomabipolar disorderopen-angle glaucomamathematical ability
✦AI Summary

THSD7A (thrombospondin type 1 domain containing 7A) is a podocyte surface antigen that functions as a target of pathogenic circulating autoantibodies in membranous nephropathy (MN) 1. The soluble form promotes endothelial cell migration and filopodia formation during sprouting angiogenesis via a FAK-dependent mechanism, operating through actin cytoskeleton organization. In disease pathology, anti-THSD7A autoantibodies form immune complexes that accumulate along the glomerular basement membrane's subepithelial region, driving MN development 2. Anti-THSD7A antibodies account for 3-5% of primary MN cases, with diagnostic and prognostic significance comparable to anti-PLA2R antibodies 21. Serum anti-THSD7A antibody levels serve as important biomarkers correlating with disease severity and treatment response, with proteinuria persistence possible months after antibody clearance 2. These autoantibodies are causative agents in MN pathogenesis 1. Clinical management involves monitoring circulating autoantibodies to guide immunosuppressive therapy decisions, with B-cell depletion agents like rituximab showing efficacy in depleting anti-THSD7A levels 3. The identification of THSD7A as a pathogenic antigen has enabled more precise molecular diagnosis and improved disease management strategies for primary membranous nephropathy.

Sources cited
1
Anti-THSD7A antibodies present in 3-5% of primary MN cases; antibody levels correlate with disease severity and clinical outcomes
PMID: 28550082
2
THSD7A identified in 2014 as podocyte surface antigen; anti-THSD7A autoantibodies are causative to MN and serve as biomarkers
PMID: 33808418
3
THSD7A is a pathogenic circulating autoantigen on glomerular podocyte surface driving autoimmunity in primary MN
PMID: 35484394
4
Rituximab treatment effectively depletes anti-PLA2R/THSD7A-like autoantibodies and serves as biomarker for treatment effect
PMID: 27352623
5
THSD7A identified as target antigen in MN; ability to monitor circulating autoantibodies aids disease monitoring and treatment decisions
PMID: 33487481
Disease Associationsⓘ20
glaucomaOpen Targets
0.48Moderate
bipolar disorderOpen Targets
0.48Moderate
open-angle glaucomaOpen Targets
0.48Moderate
mathematical abilityOpen Targets
0.42Moderate
placenta praeviaOpen Targets
0.39Weak
corneal dystrophyOpen Targets
0.39Weak
Fuchs' endothelial dystrophyOpen Targets
0.37Weak
Fuchs endothelial corneal dystrophyOpen Targets
0.36Weak
ulcerative colitisOpen Targets
0.34Weak
inflammatory bowel diseaseOpen Targets
0.34Weak
bipolar I disorderOpen Targets
0.34Weak
response to anticonvulsantOpen Targets
0.32Weak
cataractOpen Targets
0.32Weak
coronary artery diseaseOpen Targets
0.32Weak
Abruptio PlacentaeOpen Targets
0.32Weak
sialolithiasisOpen Targets
0.32Weak
COVID-19Open Targets
0.32Weak
severe acute respiratory syndromeOpen Targets
0.32Weak
lens diseaseOpen Targets
0.31Weak
Age-related cataractOpen Targets
0.31Weak
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
FLNBShared pathway100%SPTAN1Shared pathway100%ACAP1Shared pathway100%PHACTR2Shared pathway100%THSD7BShared pathway100%SPECC1Shared pathway100%
Tissue Expression6 tissues
Brain
100%
Heart
85%
Ovary
78%
Liver
59%
Lung
36%
Bone Marrow
23%
Gene Interaction Network
Click a node to explore
THSD7AFLNBSPTAN1ACAP1PHACTR2THSD7BSPECC1
PROTEIN STRUCTURE
Preparing viewer…
PDB8OXR · 2.30 Å · X-ray
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
0.50Moderately Constrained
pLIⓘ
0.01Tolerant
Observed/Expected LoF0.42 [0.35–0.50]
RankingsWhere THSD7A stands among ~20K protein-coding genes
  • #9,391of 20,598
    Most Researched46
  • #2,997of 17,882
    Most Constrained (LOEUF)0.50 · top quartile
Genes detectedTHSD7A
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Primary Membranous Nephropathy.
PMID: 28550082
Clin J Am Soc Nephrol · 2017
1.00
2
Membranous Nephropathy: Core Curriculum 2021.
PMID: 33487481
Am J Kidney Dis · 2021
0.90
3
Mechanisms of Primary Membranous Nephropathy.
PMID: 33808418
Biomolecules · 2021
0.80
4
New 'Antigens' in Membranous Nephropathy.
PMID: 33380523
J Am Soc Nephrol · 2021
0.70
5
Membranous nephropathy-diagnosis and identification of target antigens.
PMID: 37863839
Nephrol Dial Transplant · 2024
0.60