LINC01930

Summary

LINC01930 (long intergenic non-protein coding RNA 1930, HGNC:52744) is a long non-coding RNA gene on chromosome 1p21.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:52744
Approved symbol	LINC01930
Name	long intergenic non-protein coding RNA 1930
Location	1p21.3
Locus type	RNA, long non-coding
Status	Approved
Aliases	EU358092
Entrez	109729128
RNAcentral	URS0000BC4572 — lncRNA, 864 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): RS1000962004 (1:97940575 A>C,G), RS1001507727 (1:97937025 T>A), RS1001557860 (1:97940293 T>C), RS1002363936 (1:97935670 T>C), RS1002365923 (1:97941491 T>G), RS1002377076 (1:97941273 G>A), RS1002456787 (1:97935524 ATAT>A), RS1002605687 (1:97937364 G>A), RS1002675574 (1:97935889 G>T), RS1002836080 (1:97941066 T>A,C), RS1003060254 (1:97943402 C>T), RS1003132570 (1:97938166 C>A,T), RS1003184924 (1:97938385 A>G), RS1003499171 (1:97943635 G>A,C), RS1004455867 (1:97935851 C>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.