CACNA1B-AS1
gene geneOn this page
Summary
CACNA1B-AS1 (CACNA1B antisense RNA 1, HGNC:56165) is a long non-coding RNA gene on chromosome 9q34.3.
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:56165 |
| Approved symbol | CACNA1B-AS1 |
| Name | CACNA1B antisense RNA 1 |
| Location | 9q34.3 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Entrez | 105376331 |
| RNAcentral | URS00008E3A3A — lncRNA, 1951 nt, 1 organism(s) |
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
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:
dbSNP variants (sampled 300 via entrez): RS1001714577 (9:137948134 C>G,T), RS1002612943 (9:137947158 G>A), RS1002645401 (9:137947485 A>C), RS1003390536 (9:137946378 C>T), RS1004023750 (9:137946467 A>T), RS1004111296 (9:137946553 T>G), RS1004165295 (9:137946790 C>G,T), RS1005099925 (9:137948415 T>C), RS1005599974 (9:137943883 GCACAGTCATGAGTTTGCC>G), RS1005710811 (9:137945379 G>T), RS1006118095 (9:137943451 T>C), RS1006649204 (9:137944761 T>C), RS1007027481 (9:137944411 C>G), RS1007431156 (9:137943239 C>T), RS1007791182 (9:137943602 T>C)
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.