INTS12-AS1

Summary

INTS12-AS1 (INTS12 antisense RNA 1, HGNC:58863) is a long non-coding RNA gene on chromosome 4q24.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:58863
Approved symbol	INTS12-AS1
Name	INTS12 antisense RNA 1
Location	4q24
Locus type	RNA, long non-coding
Status	Approved
Entrez	124900748

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): RS1000025192 (4:105701632 A>G), RS1000494007 (4:105703180 C>A,T), RS1000539314 (4:105703488 T>C), RS1000873081 (4:105698118 A>G), RS1001526758 (4:105704211 C>T), RS1001629972 (4:105702061 C>T), RS10016392 (4:105701606 C>T), RS1001756956 (4:105701637 T>C), RS1002104605 (4:105701303 C>T), RS1002602356 (4:105704952 C>T), RS1003235673 (4:105700520 A>C), RS1003502553 (4:105703807 C>T), RS1003567306 (4:105698761 C>T), RS1003638482 (4:105706087 T>G), RS1004596869 (4:105705464 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.