SERPINB9-AS1

Summary

SERPINB9-AS1 (SERPINB9 antisense RNA 1, HGNC:56120) is a long non-coding RNA gene on chromosome 6p25.2.

At a glance

• Clinical variants (ClinVar): 5 total

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56120
Approved symbol	SERPINB9-AS1
Name	SERPINB9 antisense RNA 1
Location	6p25.2
Locus type	RNA, long non-coding
Status	Approved
Entrez	101927730
RNAcentral	URS000075A1AF — lncRNA, 650 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

5 variants total. Per-class counts are floors (≥ shown; pagination cap):

Classification	Count (floor)
Pathogenic	0
Likely pathogenic	0
Uncertain significance	0
Likely benign	1
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): RS1000215878 (6:2898712 G>A), RS1000283336 (6:2889893 G>A), RS1000415054 (6:2885529 A>G), RS1000500820 (6:2896332 A>G), RS1000548267 (6:2887180 A>T), RS1000619661 (6:2885838 G>A), RS1000697814 (6:2886861 G>A), RS1000725060 (6:2892113 A>C), RS1000732860 (6:2895183 G>A,C), RS1001252022 (6:2883630 CATTTTTT>C), RS1001458819 (6:2889583 T>C), RS1001533585 (6:2885681 T>C), RS1001570067 (6:2898201 G>T), RS1001905400 (6:2899004 A>T), RS1002104739 (6:2898786 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.