LINC01430

Summary

LINC01430 (long intergenic non-protein coding RNA 1430, HGNC:50742) is a long non-coding RNA gene on chromosome 20q13.12.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50742
Approved symbol	LINC01430
Name	long intergenic non-protein coding RNA 1430
Location	20q13.12
Locus type	RNA, long non-coding
Status	Approved
Aliases	lncRNA-DAW
Entrez	101927242
RNAcentral	URS000075AD66 — lncRNA, 442 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): RS1001010059 (20:44448659 G>A), RS1001389502 (20:44452281 T>C), RS1002704953 (20:44449770 C>T), RS1004121021 (20:44448976 G>A), RS1004173424 (20:44448692 A>G), RS1005115366 (20:44448277 T>C), RS1005484889 (20:44449395 C>A,T), RS1005579664 (20:44449795 G>A,C,T), RS1005795676 (20:44450432 C>T), RS1005914779 (20:44451317 C>T), RS1006123039 (20:44451722 G>T), RS1006702741 (20:44450300 C>T), RS1008378414 (20:44451745 C>A,T), RS1009664823 (20:44449023 G>A), RS1009797597 (20:44452444 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.