THSD4-AS2

Summary

THSD4-AS2 (THSD4 antisense RNA 2, HGNC:51421) is a long non-coding RNA gene on chromosome 15q23.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:51421
Approved symbol	THSD4-AS2
Name	THSD4 antisense RNA 2
Location	15q23
Locus type	RNA, long non-coding
Status	Approved
Entrez	101929173
RNAcentral	URS000075E7A4 — lncRNA, 2139 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): RS1000118994 (15:71688585 A>G), RS1000448512 (15:71691965 C>T), RS1000498867 (15:71691777 G>A), RS1000825578 (15:71689056 C>T), RS1001673518 (15:71691621 A>G), RS1002124107 (15:71691391 C>G), RS1002215702 (15:71692450 T>C), RS1002310160 (15:71688392 A>G), RS1002528673 (15:71691369 C>T), RS1002768990 (15:71691064 G>A), RS1003392319 (15:71690100 T>G), RS1004788221 (15:71692751 C>T), RS1004844118 (15:71692346 G>A), RS1005115391 (15:71693173 G>A), RS1005347932 (15:71689751 G>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.