LINC02992

Summary

LINC02992 (long intergenic non-protein coding RNA 2992, HGNC:49287) is a long non-coding RNA gene on chromosome 2q14.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:49287
Approved symbol	LINC02992
Name	long intergenic non-protein coding RNA 2992
Location	2q14.1
Locus type	RNA, long non-coding
Status	Approved
Entrez	100499194
RNAcentral	URS000075DADD — lncRNA, 2316 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): RS1000238945 (2:113977593 A>C,G), RS1000438920 (2:113977280 A>T), RS1000952083 (2:113980969 C>T), RS1001073311 (2:113981162 A>G), RS1001161275 (2:113978935 T>G), RS1003504630 (2:113979979 C>G,T), RS1003789242 (2:113979649 G>T), RS1004045837 (2:113981002 T>TC), RS1004145900 (2:113981228 C>G), RS1004494957 (2:113981564 G>A,T), RS1004514964 (2:113980902 C>A,T), RS1004796352 (2:113980720 C>T), RS1005275160 (2:113977972 A>G), RS1006465418 (2:113978750 G>A,C), RS1007588213 (2:113979389 C>G,T)

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.