TMEM220

Chr 17

transmembrane protein 220

TMEM220 encodes a predicted membrane protein with unknown specific function. Biallelic mutations cause autosomal recessive developmental delay, seizures, and progressive neurodegeneration with onset in infancy or early childhood. The gene shows high tolerance to loss-of-function variants in the population, suggesting the pathogenic variants may have specific effects on protein function.

ResearchSummary from RefSeq
MultiplemechanismLOEUF 1.68
Clinical SummaryTMEM220
Population Constraint (gnomAD)
Low constraint (pLI 0.00) — loss-of-function variants are relatively tolerated in the population.
📋
ClinVar Variants
11 unique Pathogenic / Likely Pathogenic· 30 VUS of 50 total submissions

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint
1.68LOEUF
pLI 0.000
Z-score 0.01
OE 1.00 (0.601.68)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint
0.64Z-score
OE missense 0.80 (0.660.98)
65 obs / 81.2 exp
Tolerant

Mild missense constraint

Observed / Expected Ratios
LoF OE1.00 (0.601.68)
00.351.4
Missense OE0.80 (0.660.98)
00.61.4
Synonymous OE1.12
01.21.6
LoF obs/exp: 9 / 9.0Missense obs/exp: 65 / 81.2Syn Z: -0.51
DN
0.6840th %ile
GOF
0.74top 25%
LOF
0.2775th %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

50 submitted variants in ClinVar

Classification Summary

Pathogenic11
VUS30
Likely Benign3
Benign1
11
Pathogenic
30
VUS
3
Likely Benign
1
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
11
0
11
Likely Pathogenic
0
0
0
0
0
VUS
0
23
7
0
30
Likely Benign
0
2
0
1
3
Benign
0
1
0
0
1
Total02618145

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

View in ClinVar →

Protein Context — Lollipop Plot

TMEM220 · 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
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