LINC01265
gene geneOn this page
Summary
LINC01265 (long intergenic non-protein coding RNA 1265, HGNC:50297) is a long non-coding RNA gene on chromosome 5p13.1.
At a glance
- GWAS associations: 1
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:50297 |
| Approved symbol | LINC01265 |
| Name | long intergenic non-protein coding RNA 1265 |
| Location | 5p13.1 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Entrez | 101926904 |
| RNAcentral | URS000056C8F0 — lncRNA, 800 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): RS1000027164 (5:38716901 C>A), RS1000058141 (5:38717331 C>A,T), RS1000141734 (5:38710579 T>C), RS1000513371 (5:38710863 A>G,T), RS1000918158 (5:38716651 G>A,C), RS1000955921 (5:38719194 A>G), RS1001028100 (5:38718983 G>C), RS1001340997 (5:38711514 G>A,T), RS1001506277 (5:38718280 C>G), RS1001576281 (5:38717970 G>A), RS1002154701 (5:38717477 T>C), RS1002185712 (5:38717731 G>A), RS1002486734 (5:38718834 C>G), RS1002694962 (5:38711146 A>C), RS1003519167 (5:38721102 A>G)
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
1 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST003253_15 | Microalbuminuria | 8.000000e-06 |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 0 entries
CTD chemical–gene interactions
2 total (human), top 2 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Cadmium Chloride | decreases expression | 1 |
| Lactic Acid | decreases expression | 1 |
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.