RARB-AS1

Summary

RARB-AS1 (RARB antisense RNA 1, HGNC:54077) is a long non-coding RNA gene on chromosome 3p24.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:54077
Approved symbol	RARB-AS1
Name	RARB antisense RNA 1
Location	3p24.2
Locus type	RNA, long non-coding
Status	Approved
Entrez	105376997
RNAcentral	URS0000A764C1 — lncRNA, 561 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: 1 (showing top): chr3p24

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): RS1000645195 (3:25382671 C>A,T), RS1002265156 (3:25383554 G>T), RS1002938586 (3:25385527 G>A,C,T), RS1003132525 (3:25384545 G>C), RS1005296225 (3:25386400 G>T), RS1006266891 (3:25384597 T>C,G), RS1006582249 (3:25384146 T>C), RS1007568569 (3:25385000 A>G), RS1007635700 (3:25383140 A>G), RS1008310427 (3:25385111 C>G), RS1008540608 (3:25384645 C>A,T), RS1008574376 (3:25386365 G>C,T), RS1008899381 (3:25384165 G>A), RS1009574745 (3:25383725 C>G,T), RS1009593607 (3:25383966 A>C,G)

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.