TMEM40

Chr 3

transmembrane protein 40

TMEM40 encodes a protein predicted to be located in cellular membranes, though its specific function remains unclear. Mutations cause autosomal recessive intellectual disability with seizures and spasticity, typically presenting in early childhood. The gene shows moderate constraint against loss-of-function variants, suggesting some tolerance to complete protein loss.

ResearchSummary from RefSeq
MultiplemechanismLOEUF 1.19
Clinical SummaryTMEM40
Population Constraint (gnomAD)
Low constraint (pLI 0.00) — loss-of-function variants are relatively tolerated in the population.
📋
ClinVar Variants
22 unique Pathogenic / Likely Pathogenic· 67 VUS of 107 total submissions

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint
1.19LOEUF
pLI 0.000
Z-score 0.95
OE 0.76 (0.501.19)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint
-0.70Z-score
OE missense 1.17 (1.031.34)
153 obs / 130.4 exp
Tolerant

Tolerant to missense variation

Observed / Expected Ratios
LoF OE0.76 (0.501.19)
00.351.4
Missense OE1.17 (1.031.34)
00.61.4
Synonymous OE0.99
01.21.6
LoF obs/exp: 14 / 18.4Missense obs/exp: 153 / 130.4Syn Z: 0.04
DN
0.6649th %ile
GOF
0.6833th %ile
LOF
0.4429th %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

107 submitted variants in ClinVar

Classification Summary

Pathogenic21
Likely Pathogenic1
VUS67
Likely Benign9
Benign1
21
Pathogenic
1
Likely Pathogenic
67
VUS
9
Likely Benign
1
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
21
0
21
Likely Pathogenic
0
0
1
0
1
VUS
0
45
22
0
67
Likely Benign
0
4
5
0
9
Benign
0
0
1
0
1
Total04950099

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

View in ClinVar →

Protein Context — Lollipop Plot

TMEM40 · 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 2 results · since 2015Search PubMed ↗