NXTAR

Summary

NXTAR (negative expression of androgen receptor regulating lncRNA, HGNC:56212) is a long non-coding RNA gene on chromosome Xq12.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:56212
Approved symbol	NXTAR
Name	negative expression of androgen receptor regulating lncRNA
Location	Xq12
Locus type	RNA, long non-coding
Status	Approved
Entrez	105373241

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): RS1000000365 (X:67770710 G>A,T), RS1000159694 (X:67750989 G>T), RS1000213181 (X:67778621 G>C,T), RS1000244121 (X:67778152 G>A), RS1000253305 (X:67764206 G>A), RS1000351251 (X:67768259 ATTT>A), RS1000357285 (X:67757698 G>A,T), RS1000518323 (X:67777904 C>T), RS1000605705 (X:67783513 A>T), RS1000741227 (X:67783227 A>G), RS1000853630 (X:67762536 C>T), RS1000865927 (X:67761541 G>T), RS1000875757 (X:67761342 A>G), RS1000949771 (X:67775990 A>G,T), RS1000998678 (X:67769035 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.