ENOX2-AS1

Summary

ENOX2-AS1 (ENOX2 antisense RNA 1, HGNC:56096) is a long non-coding RNA gene on chromosome Xq26.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56096
Approved symbol	ENOX2-AS1
Name	ENOX2 antisense RNA 1
Location	Xq26.1
Locus type	RNA, long non-coding
Status	Approved
Entrez	105373338
RNAcentral	URS0000A770FF — lncRNA, 928 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

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): RS1001656893 (X:130802414 C>T), RS1001749204 (X:130806547 T>G), RS1003025771 (X:130803811 G>A), RS1003046739 (X:130804413 C>T), RS1003421332 (X:130803221 T>C), RS1003783963 (X:130802124 C>A), RS1004082311 (X:130805499 T>C), RS1004982469 (X:130806832 G>A), RS1005153844 (X:130802706 G>C), RS1006192157 (X:130805754 T>C), RS1006511836 (X:130803137 G>A,T), RS1007019550 (X:130802957 T>C,G), RS1007378108 (X:130805080 C>T), RS1008950390 (X:130805000 T>C), RS1010794692 (X:130802475 T>A)

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.