TMEM192

Chr 4

transmembrane protein 192

This gene encodes a protein that enables homodimerization and localizes to late endosomes and lysosomal membranes. Mutations cause spastic paraplegia with intellectual disability, typically with autosomal recessive inheritance. The gene appears tolerant to loss-of-function variants based on population genetics data.

Summary from RefSeq
Research Assistant →
0
Active trials
8
Pubs (1 yr)
44
P/LP submissions
0%
P/LP missense
1.29
LOEUF
Multiple*
Mechanism· predicted
Clinical SummaryTMEM192
Population Constraint (gnomAD)
Low constraint (pLI 0.00) — loss-of-function variants are relatively tolerated in the population.
📋
ClinVar Variants
44 unique Pathogenic / Likely Pathogenic· 39 VUS of 95 total submissions

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint
1.29LOEUF
pLI 0.000
Z-score 0.81
OE 0.76 (0.471.29)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint
-0.08Z-score
OE missense 1.02 (0.891.17)
146 obs / 143.5 exp
Tolerant

Tolerant to missense variation

Observed / Expected Ratios
LoF OE0.76 (0.471.29)
00.351.4
Missense OE1.02 (0.891.17)
00.61.4
Synonymous OE0.88
01.21.6
LoF obs/exp: 10 / 13.2Missense obs/exp: 146 / 143.5Syn Z: 0.70
DN
0.7034th %ile
GOF
0.6638th %ile
LOF
0.2970th %ile

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

DNprediction above median
GOFprediction 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

95 submitted variants in ClinVar

Classification Summary

Pathogenic42
Likely Pathogenic2
VUS39
Likely Benign1
Benign1
42
Pathogenic
2
Likely Pathogenic
39
VUS
1
Likely Benign
1
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
42
0
42
Likely Pathogenic
0
0
2
0
2
VUS
0
32
7
0
39
Likely Benign
0
1
0
0
1
Benign
0
0
1
0
1
Total03352085

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

View in ClinVar →

Protein Context — Lollipop Plot

TMEM192 · 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.

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Clinical Literature
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