LMX1B-DT

Chr 9

LMX1B divergent transcript

I cannot provide a clinical summary for LMX1B-DT as no functional, phenotypic, or inheritance information has been provided in the data below. LMX1B-DT appears to be a non-coding transcript associated with the LMX1B locus, but without specific information about its role in disease or protein function, a clinically useful summary cannot be written.

Clinical SummaryLMX1B-DT
📋
ClinVar Variants
17 unique Pathogenic / Likely Pathogenic· 1 VUS of 18 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

18 submitted variants in ClinVar

Classification Summary

Pathogenic17
VUS1
17
Pathogenic
1
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
17
Likely Pathogenic
0
VUS
1
Likely Benign
0
Benign
0
Total18

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

LMX1B-DT · 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 →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found