GCASPC
gene geneOn this page
Also known as TCONS_00011605RP1-56L9.7-001lnc-SOD2-1
Summary
GCASPC (gall bladder cancer associated suppressor of pyruvate carboxylase lncRNA, HGNC:52281) is a long non-coding RNA gene on chromosome 6q25.3.
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:52281 |
| Approved symbol | GCASPC |
| Name | gall bladder cancer associated suppressor of pyruvate carboxylase lncRNA |
| Location | 6q25.3 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Aliases | TCONS_00011605, RP1-56L9.7-001, lnc-SOD2-1 |
| Entrez | 112441427 |
Gene structure
Transcript identifiers
Ensembl transcripts: 0
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
None — 0 exons
Expression profiles
Top tissues by expression
0 total, by Bgee expression score (0-100, higher = more expressed):
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 1)
- we characterized the clinicopathologic relevance of a novel gallbladder cancer-associated suppressor of pyruvate carboxylase lncRNA (lncRNA GCASPC) in gallbladder cancer progression (PMID:27450454)
Cross-species orthologs
0 orthologs
Protein
Protein identifiers
Canonical reviewed UniProt: None (reviewed: )
All UniProt accessions (0):
RefSeq proteins (0): (*=MANE)
Domains & families (InterPro)
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 0 (showing top):
GO Biological Process (0):
GO Molecular Function (0):
GO Cellular Component (0):
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
0 interactions, top by confidence:
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
0 scored. Top likely-pathogenic:
Disease associations
OMIM: gene `` | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
0 associations (top):
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 0 entries
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.