LINC03035

Summary

LINC03035 (long intergenic non-protein coding RNA 3035, HGNC:56211) is a long non-coding RNA gene on chromosome 18q21.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56211
Approved symbol	LINC03035
Name	long intergenic non-protein coding RNA 3035
Location	18q21.2
Locus type	RNA, long non-coding
Status	Approved
Entrez	105372125

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): RS1000654489 (18:55082673 C>T), RS1000711913 (18:55086313 T>C), RS1000722401 (18:55081210 C>T), RS1000852287 (18:55079366 C>A,G), RS1000940023 (18:55083059 A>G), RS1001329330 (18:55079875 G>C), RS1001340617 (18:55086331 C>G), RS1001372720 (18:55086191 A>G), RS1001494272 (18:55079564 G>A,T), RS1001704799 (18:55085549 G>A), RS1001775367 (18:55085896 A>G), RS1002030111 (18:55079639 G>C), RS1002040415 (18:55086871 T>C), RS1002113888 (18:55087266 G>A,C), RS1002605713 (18:55081760 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

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.