PDCD6IP-DT

Chr 3

PDCD6IP divergent transcript

NCBI Gene: 105377023ENSG00000271643

I cannot provide a clinical summary for PDCD6IP-DT as no functional or clinical information has been provided in the data. This appears to be a non-coding transcript variant that would require specific research literature and clinical evidence to characterize its role in pediatric neurological disease.

Research
Clinical Summary— PDCD6IP-DT
📋
ClinVar Variants
7 unique Pathogenic / Likely Pathogenic of 7 total submissions
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Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

7 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic7
7
Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————7
Likely Pathogenic
————0
VUS
————0
Likely Benign
————0
Benign
————0
Total—7

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

PDCD6IP-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