ADAMTS16-DT

Chr 5

ADAMTS16 divergent transcript

Also known as: CTD-2297D10.2

NCBI Gene: 101929176ENSG00000250579

I cannot provide a clinical summary for ADAMTS16-DT based on the provided information. ADAMTS16-DT appears to be a long non-coding RNA transcript associated with the ADAMTS16 gene rather than a protein-coding gene, and no clinical data, protein function, associated diseases, or inheritance patterns have been provided for this transcript.

Research
Clinical Summary— ADAMTS16-DT
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ClinVar Variants
50 unique Pathogenic / Likely Pathogenic of 50 total submissions
Explore recent and relevant literature in Research Assistant →

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

50 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic50
50
Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————50
Likely Pathogenic
————0
VUS
————0
Likely Benign
————0
Benign
————0
Total—50

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

ADAMTS16-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

ClinicalTrials.gov

No active trials found for this gene.

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External Resources

Links to major genomics databases and tools

Franklin by Genoox
AI-powered variant curation and clinical analysis
DECIPHER
Genomic variants and phenotypes in rare disease patients