MANCR

Chr 10

mitotically associated long non coding RNA

Also known as: LINC00704

I cannot provide a clinical gene summary for MANCR as no information about this gene's protein function, associated diseases, or inheritance pattern was provided in the data below the instructions.

Clinical SummaryMANCR
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ClinVar Variants
13 unique Pathogenic / Likely Pathogenic· 1 VUS of 15 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

15 submitted variants in ClinVar

Classification Summary

Pathogenic11
Likely Pathogenic2
VUS1
Benign1
11
Pathogenic
2
Likely Pathogenic
1
VUS
1
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
11
Likely Pathogenic
2
VUS
1
Likely Benign
0
Benign
1
Total15

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

MANCR · 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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