PANX3

Chr 11

pannexin 3

Also known as: PX3

This protein functions as a calcium channel in the endoplasmic reticulum that regulates osteoblast differentiation and allows ATP release into extracellular space. Mutations cause autosomal dominant oculodentodigital dysplasia, a syndromic condition affecting the eyes, teeth, and digits. The gene is not highly constrained against loss-of-function variants.

Summary from RefSeq, UniProt
Research Assistant →
0
Active trials
13
Pubs (1 yr)
60
P/LP submissions
0%
P/LP missense
1.08
LOEUF
Multiple*
Mechanism· predicted
Clinical SummaryPANX3
Population Constraint (gnomAD)
Low constraint (pLI 0.00) — loss-of-function variants are relatively tolerated in the population.
📋
ClinVar Variants
60 unique Pathogenic / Likely Pathogenic· 50 VUS of 115 total submissions

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint
1.08LOEUF
pLI 0.000
Z-score 1.35
OE 0.62 (0.371.08)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint
0.47Z-score
OE missense 0.91 (0.811.02)
206 obs / 225.7 exp
Tolerant

Mild missense constraint

Observed / Expected Ratios
LoF OE0.62 (0.371.08)
00.351.4
Missense OE0.91 (0.811.02)
00.61.4
Synonymous OE0.91
01.21.6
LoF obs/exp: 9 / 14.6Missense obs/exp: 206 / 225.7Syn Z: 0.68
DN
0.7228th %ile
GOF
0.75top 25%
LOF
0.2091th %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

115 submitted variants in ClinVar

Classification Summary

Pathogenic58
Likely Pathogenic2
VUS50
Likely Benign2
Benign1
58
Pathogenic
2
Likely Pathogenic
50
VUS
2
Likely Benign
1
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
58
0
58
Likely Pathogenic
0
0
2
0
2
VUS
0
44
6
0
50
Likely Benign
0
1
0
1
2
Benign
0
1
0
0
1
Total046661113

LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

PANX3 · protein map & ClinVar variants

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

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
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Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
PubTator3
Top 5 full-text resultsSearch PubTator3 ↗