DOCK9-DT

Chr 13

DOCK9 divergent transcript

Also known as: DOCK9-AS2

I cannot write a clinical gene summary for DOCK9-DT based on the provided information. DOCK9-DT appears to be a non-coding transcript or pseudogene rather than a protein-coding gene, and no clinical data, protein function, associated diseases, or inheritance patterns were provided in the input data to support a meaningful clinical summary.

Clinical SummaryDOCK9-DT
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ClinVar Variants
30 unique Pathogenic / Likely Pathogenic· 1 VUS of 31 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

31 submitted variants in ClinVar

Classification Summary

Pathogenic30
VUS1
30
Pathogenic
1
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
30
Likely Pathogenic
0
VUS
1
Likely Benign
0
Benign
0
Total31

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

DOCK9-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