DOCK7-DT

Chr 1

DOCK7 divergent transcript

I cannot provide a clinical gene summary for DOCK7-DT as this appears to be a non-coding transcript or pseudogene rather than a protein-coding gene, and no information about its function, associated diseases, or inheritance patterns was provided in the data below.

Research

ResearchGenerating clinical summary…

Clinical Summary— DOCK7-DT

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ClinVar Variants

1 total variants — no pathogenic classifications of 1 total submissions

Explore recent and relevant literature in Research Assistant →

Some data sources returned errors (1)

omim: Error: OMIM fetch failed: 429

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

1 submitted variants in ClinVar

ClinVar

Classification Summary

Likely Benign1

Likely Benign

Curated Variants Distribution

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

Classification	LoF	Missense + Inframe	Non-coding	Synonymous	Total
Pathogenic	—	—	—	—	0
Likely Pathogenic	—	—	—	—	0
VUS	—	—	—	—	0
Likely Benign	—	—	—	—	1
Benign	—	—	—	—	0
Total	—				1

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

11 pathogenic / likely-pathogenic (of 12) ClinVar copy-number / structural variants overlap DOCK7-DT — these span large chromosomal regions, not the gene specifically, and are excluded from the counts above. Explore in CNV tools →