STPG3

Chr 9

sperm-tail PG-rich repeat containing 3

Also known as: C9orf173

This gene encodes a protein predicted to be active in the cytoskeleton, though its specific function remains unclear. Mutations cause autosomal recessive intellectual disability with seizures and spasticity, typically presenting in infancy or early childhood. The gene shows minimal constraint against loss-of-function variants, consistent with the recessive inheritance pattern observed in affected families.

ResearchSummary from RefSeq
MultiplemechanismLOEUF 1.73
Clinical SummarySTPG3
Population Constraint (gnomAD)
Low constraint (pLI 0.00) — loss-of-function variants are relatively tolerated in the population.
📋
ClinVar Variants
98 unique Pathogenic / Likely Pathogenic· 9 VUS of 120 total submissions

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint
1.73LOEUF
pLI 0.000
Z-score -0.62
OE 1.18 (0.801.73)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint
-0.44Z-score
OE missense 1.08 (0.971.21)
236 obs / 217.9 exp
Tolerant

Tolerant to missense variation

Observed / Expected Ratios
LoF OE1.18 (0.801.73)
00.351.4
Missense OE1.08 (0.971.21)
00.61.4
Synonymous OE1.07
01.21.6
LoF obs/exp: 17 / 14.5Missense obs/exp: 236 / 217.9Syn Z: -0.50
DN
0.6357th %ile
GOF
0.6638th %ile
LOF
0.3551th %ile

This gene has evidence for multiple mechanisms of pathogenicity (gain-of-function and dominant-negative). Both the Badonyi & Marsh prediction and the broader genomic evidence point to gain-of-function as the predominant mechanism. Different variants in this gene may act through different mechanisms — interpret in context of the specific variant.

GOFprediction above median
DNprediction above median

Note: In-silico variant effect predictors (SIFT, PolyPhen, REVEL, CADD) may underestimate pathogenicity of missense variants in genes with GOF or DN mechanisms. Consider functional evidence and clinical context.

Predictions from Badonyi M, Marsh JA. PLoS ONE. 2024;19(8):e0307312.

ClinVar Variant Classifications

120 submitted variants in ClinVar

Classification Summary

Pathogenic91
Likely Pathogenic7
VUS9
Likely Benign2
Benign3
Conflicting3
91
Pathogenic
7
Likely Pathogenic
9
VUS
2
Likely Benign
3
Benign
3
Conflicting

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
91
Likely Pathogenic
7
VUS
9
Likely Benign
2
Benign
3
Conflicting
3
Total115

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

STPG3 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

3D Protein StructureAlphaFold

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →
Key Publications
Landmark & review papers · by relevance
PubMed
Top 1 results · since 2015Search PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found