TMEM265

Chr 16

transmembrane protein 265

Also known as: IFITMD8

The protein is predicted to be a membrane-localized protein, though its specific function remains unclear. Mutations in TMEM265 cause autosomal recessive congenital disorders of glycosylation with variable presentations including developmental delay, intellectual disability, and multisystem involvement. This represents an emerging glycosylation disorder with expanding phenotypic spectrum as more cases are identified.

ResearchSummary from RefSeq
Multiplemechanism
Clinical SummaryTMEM265
📋
ClinVar Variants
4 unique Pathogenic / Likely Pathogenic of 6 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

DN
0.80top 25%
GOF
0.84top 5%
LOF
0.08100th %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

6 submitted variants in ClinVar

Classification Summary

Pathogenic4
4
Pathogenic

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
4
Likely Pathogenic
0
VUS
0
Likely Benign
0
Benign
0
Total4

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

TMEM265 · 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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