CLYBL-AS3

Summary

CLYBL-AS3 (CLYBL antisense RNA 3, HGNC:56191) is a long non-coding RNA gene on chromosome 13q32.3.

At a glance

• Clinical variants (ClinVar): 1 total

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56191
Approved symbol	CLYBL-AS3
Name	CLYBL antisense RNA 3
Location	13q32.3
Locus type	RNA, long non-coding
Status	Approved
Entrez	101927437
RNAcentral	URS000075C22B — lncRNA, 543 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

1 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): RS1000022 (13:99808965 C>T), RS1000022782 (13:99854772 G>A), RS1000026668 (13:99894195 C>A,T), RS1000035544 (13:99934617 C>T), RS1000042738 (13:99768071 C>T), RS1000055201 (13:99847098 G>A), RS1000066233 (13:99811988 C>A), RS1000074052 (13:99938445 C>T), RS1000090271 (13:99774759 G>A), RS1000106020 (13:99939668 G>A), RS1000128759 (13:99900695 C>G,T), RS1000131438 (13:99859367 C>A), RS1000133325 (13:99818446 A>C), RS1000133686 (13:99901439 C>T), RS1000165353 (13:99774388 G>A,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.