LRTM3

Chr 13

leucine rich repeat transmembrane protein 3

Also known as: C13orf40, CCDC168

LRTM3 encodes a membrane-localized protein with unknown function. No established human diseases have been definitively associated with mutations in this gene. The clinical significance of variants in LRTM3 remains uncertain.

Summary from RefSeq
Research Assistant →
0
Active trials
0
Pubs (1 yr)
10
P/LP submissions
P/LP missense
LOEUF
Mechanism
Clinical SummaryLRTM3
📋
ClinVar Variants
10 unique Pathogenic / Likely Pathogenic of 10 total submissions
Some data sources returned errors (2)

ensembl: Error: Ensembl fetch failed: 400 for https://rest.ensembl.org/lookup/symbol/homo_sapiens/LRTM3?content-type=application/json&expand=1

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

10 submitted variants in ClinVar

Classification Summary

Pathogenic10
10
Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
10
Likely Pathogenic
0
VUS
0
Likely Benign
0
Benign
0
Total10

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

LRTM3 · 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 →

No publications found for LRTM3