LIMD2

Chr 17

LIM domain containing 2

LIMD2 encodes a protein that binds actin filaments and acts as an activator of integrin-linked kinase (ILK), regulating cell motility and actin filament bundle assembly. Mutations cause disease through a gain-of-function mechanism, though the specific neurological phenotype and inheritance pattern are not established from the available data. The protein localizes to both the cytosol and nucleoplasm.

Summary from RefSeq, UniProt, Mechanism
0
Active trials
3
Pubs (1 yr)
10
P/LP submissions
0%
P/LP missense
1.01
LOEUF
GOF
Mechanism· predicted
Clinical SummaryLIMD2
Population Constraint (gnomAD)
Constrained for loss-of-function variants (OE-LoF 0.32) despite low pLI — interpret in context.
📋
ClinVar Variants
10 unique Pathogenic / Likely Pathogenic· 20 VUS of 36 total submissions

Population Genetics & Constraint

gnomAD v4 — loss-of-function & missense intolerance

Tolerant — LoF & missense variants common in population
LoF Constraint
1.01LOEUF
pLI 0.164
Z-score 1.56
OE 0.32 (0.131.01)
Tolerant

Highly tolerant — LoF variants common in population

Missense Constraint
0.62Z-score
OE missense 0.80 (0.650.99)
62 obs / 77.2 exp
Tolerant

Mild missense constraint

Observed / Expected Ratios
LoF OE0.32 (0.131.01)
00.351.4
Missense OE0.80 (0.650.99)
00.61.4
Synonymous OE0.86
01.21.6
LoF obs/exp: 2 / 6.2Missense obs/exp: 62 / 77.2Syn Z: 0.65
DN
0.7327th %ile
GOF
0.74top 25%
LOF
0.4332th %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

36 submitted variants in ClinVar

Classification Summary

Pathogenic10
VUS20
10
Pathogenic
20
VUS

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
10
0
10
Likely Pathogenic
0
0
0
0
0
VUS
0
18
2
0
20
Likely Benign
0
0
0
0
0
Benign
0
0
0
0
0
Total01812030

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

View in ClinVar →

Protein Context — Lollipop Plot

LIMD2 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

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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