TMEM42

Chr 3

transmembrane protein 42

TMEM42 encodes a protein predicted to be located in cellular membranes, though its specific function remains unclear. Mutations cause autosomal recessive developmental and epileptic encephalopathy with progressive microcephaly, typically presenting in infancy with seizures and severe developmental delays. The gene shows tolerance to loss-of-function variants in the general population, consistent with its recessive inheritance pattern.

ResearchSummary from RefSeq
MultiplemechanismLOEUF 1.40
Clinical SummaryTMEM42
Population Constraint (gnomAD)
Low constraint (pLI 0.08) — loss-of-function variants are relatively tolerated in the population.
📋
ClinVar Variants
6 unique Pathogenic / Likely Pathogenic· 33 VUS of 46 total submissions

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint
1.40LOEUF
pLI 0.081
Z-score 1.04
OE 0.46 (0.191.40)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint
0.14Z-score
OE missense 0.95 (0.781.17)
67 obs / 70.3 exp
Tolerant

Mild missense constraint

Observed / Expected Ratios
LoF OE0.46 (0.191.40)
00.351.4
Missense OE0.95 (0.781.17)
00.61.4
Synonymous OE0.99
01.21.6
LoF obs/exp: 2 / 4.4Missense obs/exp: 67 / 70.3Syn Z: 0.05
DN
0.6649th %ile
GOF
0.6639th %ile
LOF
0.3068th %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

46 submitted variants in ClinVar

Classification Summary

Pathogenic5
Likely Pathogenic1
VUS33
Likely Benign2
5
Pathogenic
1
Likely Pathogenic
33
VUS
2
Likely Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
5
0
5
Likely Pathogenic
0
0
1
0
1
VUS
0
30
3
0
33
Likely Benign
0
1
0
1
2
Benign
0
0
0
0
0
Total0319141

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

View in ClinVar →

Protein Context — Lollipop Plot

TMEM42 · 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 →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found