TNFAIP8-AS1

Summary

TNFAIP8-AS1 (TNFAIP8 antisense RNA 1, HGNC:59119) is a long non-coding RNA gene on chromosome 5q23.1.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:59119
Approved symbol	TNFAIP8-AS1
Name	TNFAIP8 antisense RNA 1
Location	5q23.1
Locus type	RNA, long non-coding
Status	Approved
Entrez	102723444

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): RS1000275441 (5:119344893 G>A), RS1000393591 (5:119340806 G>A,C,T), RS1000494714 (5:119347220 G>C), RS1000633747 (5:119356274 G>T), RS1000657667 (5:119353086 T>G), RS1000732811 (5:119340897 C>T), RS1000764724 (5:119342300 A>C), RS1000775745 (5:119347442 G>A), RS1001084895 (5:119341090 T>C), RS1001446818 (5:119339761 G>A), RS1001812033 (5:119345447 C>A), RS1001858697 (5:119356906 G>A), RS1001867467 (5:119350734 G>C), RS1001967493 (5:119351028 G>T), RS1002339690 (5:119354262 G>A,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.