SMUG1-AS1

Summary

SMUG1-AS1 (SMUG1 antisense RNA 1, HGNC:53307) is a long non-coding RNA gene on chromosome 12q13.13.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:53307
Approved symbol	SMUG1-AS1
Name	SMUG1 antisense RNA 1
Location	12q13.13
Locus type	RNA, long non-coding
Status	Approved
Ensembl gene	ENSG00000283073
Entrez	105369776

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): RS1000015027 (12:54149034 C>A,T), RS1000015516 (12:54143413 T>C), RS1000199742 (12:54142623 A>G,T), RS1000472926 (12:54148751 T>C), RS1000512213 (12:54147607 C>A), RS1001061646 (12:54142414 T>A,G), RS1001072692 (12:54147188 C>T), RS1001344534 (12:54148656 C>A,T), RS1001910301 (12:54144249 T>A), RS1001990329 (12:54146982 C>A), RS1002417762 (12:54141259 G>A,C), RS1002579379 (12:54146874 C>G,T), RS1002702440 (12:54141030 C>A), RS1002878056 (12:54152426 T>C), RS1002991788 (12:54145605 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.