CDRT7
Chr 17CMT1A duplicated region transcript 7
Also known as: LINC00025, NCRNA00025
I don't have sufficient information provided about the CDRT7 gene to write a clinical summary following the strict rules you've outlined. To create an accurate 2-3 sentence summary, I would need specific data about the protein function, associated diseases/phenotypes, inheritance pattern, and any constraint metrics (pLI/LOEUF) for this gene. Could you please provide the clinical and functional information for CDRT7?
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
42 submitted variants in ClinVar
Classification Summary
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | — | — | — | — | 38 |
Likely Pathogenic | — | — | — | — | 4 |
VUS | — | — | — | — | 0 |
Likely Benign | — | — | — | — | 0 |
Benign | — | — | — | — | 0 |
| Total | — | 42 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
CDRT7 · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
3D Protein StructureAlphaFold
External Resources
Links to major genomics databases and tools
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →No open access results found
External Resources
Links to major genomics databases and tools