BANCR

Chr 9

BRAF-activated non-protein coding RNA

Also known as: LINC00586

This gene encodes a long non-coding RNA that regulates epithelial to mesenchymal transition through MAP kinase signaling pathways. Currently, no Mendelian diseases have been definitively associated with mutations in this gene. The inheritance pattern for any potential disease associations remains to be established.

OMIMResearchSummary from RefSeq
Clinical SummaryBANCR
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ClinVar Variants
41 unique Pathogenic / Likely Pathogenic· 12 VUS of 59 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

59 submitted variants in ClinVar

Classification Summary

Pathogenic33
Likely Pathogenic8
VUS12
Likely Benign2
33
Pathogenic
8
Likely Pathogenic
12
VUS
2
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
33
Likely Pathogenic
8
VUS
12
Likely Benign
2
Benign
0
Total55

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

BANCR · 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
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