LINC02083

Summary

LINC02083 (long intergenic non-protein coding RNA 2083, HGNC:52933) is a long non-coding RNA gene on chromosome 3q25.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:52933
Approved symbol	LINC02083
Name	long intergenic non-protein coding RNA 2083
Location	3q25.2
Locus type	RNA, long non-coding
Status	Approved
Entrez	107986147

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): RS1000007043 (3:153441625 G>A), RS1000338530 (3:153441968 C>CT), RS1000661684 (3:153436435 C>T), RS1000798352 (3:153436632 T>A), RS1000871426 (3:153439931 G>A,C), RS1000951734 (3:153443282 C>A,T), RS1001305043 (3:153435632 C>T), RS1001382797 (3:153443068 G>A,C), RS1001400739 (3:153442523 A>C), RS1001433311 (3:153442143 G>A), RS1001672610 (3:153435922 G>C), RS1002031852 (3:153438760 A>G), RS1002090083 (3:153431591 G>A), RS1002432758 (3:153443437 C>T), RS1002875048 (3:153437014 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.