SLC30A6-DT

Chr 2

SLC30A6 divergent transcript

I cannot provide a clinical gene summary for SLC30A6-DT because no functional, phenotypic, or inheritance information was provided in the data. SLC30A6-DT appears to be a non-coding RNA transcript associated with the SLC30A6 gene region, but without specific information about its role or associated diseases, I cannot make clinically relevant statements about this gene.

Clinical SummarySLC30A6-DT
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ClinVar Variants
17 unique Pathogenic / Likely Pathogenic· 2 VUS of 20 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

20 submitted variants in ClinVar

Classification Summary

Pathogenic17
VUS2
Benign1
17
Pathogenic
2
VUS
1
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
17
Likely Pathogenic
0
VUS
2
Likely Benign
0
Benign
1
Total20

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SLC30A6-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.

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Clinical Literature
Open Research Assistant →
Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
PubTator3
Top 5 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found