LINC03001
gene geneOn this page
Also known as TCONS_00011222
Summary
LINC03001 (long intergenic non-protein coding RNA 3001, HGNC:56118) is a long non-coding RNA gene on chromosome 6p11.2.
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:56118 |
| Approved symbol | LINC03001 |
| Name | long intergenic non-protein coding RNA 3001 |
| Location | 6p11.2 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Aliases | TCONS_00011222 |
| Entrez | 100506188 |
| RNAcentral | URS000075B82C — lncRNA, 1460 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): RS1000338469 (6:57260036 A>G), RS1001559192 (6:57261434 A>G), RS1001657653 (6:57261942 C>T), RS1002926962 (6:57260377 T>C), RS1003241532 (6:57262728 C>T), RS1003283658 (6:57260636 G>A,C), RS1004798558 (6:57264519 A>T), RS1004990364 (6:57265262 G>A), RS1005984769 (6:57260748 T>C), RS1006124828 (6:57261061 A>G), RS1006268975 (6:57263490 G>A,C), RS1007922495 (6:57265033 T>C), RS1008067206 (6:57261453 A>C), RS1008156777 (6:57261114 G>A), RS1008209710 (6:57262339 G>A)
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
CTD chemical–gene interactions
1 total (human), top 1 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Smoke | increases 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.