ADGRV1-AS1

Summary

ADGRV1-AS1 (ADGRV1 antisense RNA 1, HGNC:59094) is a long non-coding RNA gene on chromosome 5q14.3.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:59094
Approved symbol	ADGRV1-AS1
Name	ADGRV1 antisense RNA 1
Location	5q14.3
Locus type	RNA, long non-coding
Status	Approved
Entrez	105379077

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): RS1000052420 (5:90724184 T>C), RS1000285802 (5:90726129 G>A,T), RS1000436930 (5:90731889 C>A,G), RS1000492113 (5:90729046 A>C,T), RS1000509591 (5:90727212 C>G,T), RS1000607519 (5:90721292 C>T), RS1000614652 (5:90732909 G>A,T), RS1000740657 (5:90734899 A>G,T), RS1000772996 (5:90733236 C>T), RS1000988128 (5:90716339 A>G), RS1001007302 (5:90723048 A>G), RS1001085541 (5:90714969 A>C,T), RS1001173331 (5:90726894 T>C), RS1001458227 (5:90722773 A>G), RS1001718225 (5:90723505 CTTAA>C)

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.