PCAT7
Chr 9prostate cancer associated transcript 7
I cannot provide a clinical summary for PCAT7 as no information about this gene's protein function, associated diseases, or inheritance pattern has been provided in the data below the instructions. The gene appears to be a pseudogene or long non-coding RNA (based on the "PCAT" prefix typically indicating "Prostate Cancer Associated Transcript"), but without specific functional and clinical data, I cannot create an accurate clinical summary following the strict rules provided.
Some data sources returned errors (1)
ncbi: Error: NCBI fetch failed: 429 https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
58 submitted variants in ClinVar
Classification Summary
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | 0 | 0 | 14 | 0 | 14 |
Likely Pathogenic | 0 | 0 | 0 | 0 | 0 |
VUS | 0 | 32 | 1 | 0 | 33 |
Likely Benign | 0 | 1 | 0 | 1 | 2 |
Benign | 1 | 2 | 0 | 1 | 4 |
| Total | 1 | 35 | 15 | 2 | 53 |
LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
PCAT7 · 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 →External Resources
Links to major genomics databases and tools