IGF2-AS

gene
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Also known as PEG8IGF2-AS1

Summary

IGF2-AS (IGF2 antisense RNA, HGNC:14062) is a long non-coding RNA gene on chromosome 11p15.5.

This gene is expressed in antisense to the insulin-like growth factor 2 (IGF2) gene and is imprinted and paternally expressed. It is thought to be non-coding because the putative protein is not conserved and translation is predicted to trigger nonsense mediated decay (NMD). Transcripts from this gene are produced in tumors and may function to suppress cell growth. Alternative splicing results in multiple transcript variants.

Source: NCBI Gene 51214 — RefSeq curated summary.

At a glance

  • Gene type: non-coding (lncRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:14062
Approved symbolIGF2-AS
NameIGF2 antisense RNA
Location11p15.5
Locus typeRNA, long non-coding
StatusApproved
AliasesPEG8, IGF2-AS1
Ensembl geneENSG00000099869
Ensembl biotypelncRNA
OMIM610146
Entrez51214
RNAcentralURS0000A76E5D — lncRNA, 2107 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 3 — 3 lncRNA

ENST00000381361, ENST00000381363, ENST00000445504

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000381361 — 3 exons

ExonStartEnd
ENSE0000128722521473182148666
ENSE0000148841321462452146527
ENSE0000192644821405172140947

Expression profiles

Bgee: expression breadth ubiquitous, 122 present calls, max score 83.76.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0786 / max 13.4976, expressed in 41 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1126710.051834
1126700.026915

Top tissues by expression

252 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
pancreatic ductal cellCL:000207983.76silver quality
triceps brachiiUBERON:000150980.53gold quality
gluteal muscleUBERON:000200080.26gold quality
skeletal muscle tissue of rectus abdominisUBERON:000451179.77gold quality
gingival epitheliumUBERON:000194979.05gold quality
adrenal tissueUBERON:001830376.23gold quality
gingivaUBERON:000182875.88gold quality
dorsal motor nucleus of vagus nerveUBERON:000287074.39silver quality
diaphragmUBERON:000110373.08gold quality
tonsilUBERON:000237272.28gold quality
inferior olivary complexUBERON:000212771.71gold quality
tongue squamous epitheliumUBERON:000691971.57gold quality
vena cavaUBERON:000408771.56gold quality
cartilage tissueUBERON:000241870.16silver quality
secondary oocyteCL:000065569.84gold quality
placentaUBERON:000198768.75gold quality
amniotic fluidUBERON:000017368.62gold quality
deciduaUBERON:000245068.31silver quality
right lobe of liverUBERON:000111468.30gold quality
stromal cell of endometriumCL:000225568.17gold quality
vastus lateralisUBERON:000137968.08gold quality
islet of LangerhansUBERON:000000667.97gold quality
body of tongueUBERON:001187667.77gold quality
biceps brachiiUBERON:000150767.75gold quality
epithelial cell of pancreasCL:000008367.70gold quality
heart right ventricleUBERON:000208067.52gold quality
pharyngeal mucosaUBERON:000035567.51gold quality
quadriceps femorisUBERON:000137767.48gold quality
saphenous veinUBERON:000731867.32gold quality
ponsUBERON:000098867.19silver quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no1.14

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): DNMT3B, POU5F1

Literature-anchored findings (GeneRIF, showing 12)

  • IGF-IR and IGF-IIR antisense genes could significantly restrain the malignant behavior of human hepatoma cells and might be useful in investigating a potential route for hepatocellular carcinoma gene therapy. (PMID:12603530)
  • The strongest evidence for altered methylation patterns in shiftworkers was observed for IGF2AS gene. (PMID:23193016)
  • Germline variations in IGF2-AS gene were associated with prostate cancer mortality, independent of stage and Gleason score and specific to prostate cancer. (PMID:24824313)
  • IGF2-AS takes important regulatory parts in the gastric adenocarcinoma development by regulating SHOX2 via sponging miR-503.IGF2-AS is up-regulated in gastric adenocarcinoma tissues and correlated with poor prognosis. (PMID:31183590)
  • We demonstrated that inhibiting IGF2-AS, possibly also through activation of AKT signaling pathway, has a protective function in high-glucose-induced apoptosis in human retinal pigment epithelial cells in diabetic retinopathy. (PMID:31317640)
  • Data suggest that serum long non-coding RNA IGF2-AS (IGF2AS) may be a potential biomarker for the diagnosis of HBV-related hepatocellular carcinoma (HCC). (PMID:31850718)
  • Long non-coding RNA IGF2-AS represses breast cancer tumorigenesis by epigenetically regulating IGF2. (PMID:33175607)
  • lncRNA IGF2-AS promotes the osteogenic differentiation of bone marrow mesenchymal stem cells by sponging miR-3,126-5p to upregulate KLK4. (PMID:34101307)
  • Long non-coding RNA IGF2-AS promotes trophoblast cell proliferation, migration, and invasion by regulating miR-520g/N-cadherin axis. (PMID:34109707)
  • Downregulation of lncRNA IGF2-AS-encoded peptide induces trophoblast - cycle arrest. (PMID:34474977)
  • Over-expression of long non-coding RNA insulin-like growth factor 2-antisense suppressed hepatocellular carcinoma cell proliferation and metastasis by regulating the microRNA-520h/cyclin-dependent kinase inhibitor 1A signaling pathway. (PMID:34516353)
  • LncRNA IGF2-AS promotes endometriosis progression through targeting miR-370-3p/IGF2 axis and activating PI3K/AKT/mTOR signaling pathway. (PMID:36508036)

Cross-species orthologs

0 orthologs

Protein

Non-coding RNA — no protein product; not a drug target.

Function

No curated pathway, Gene-Ontology, or interaction data.

Disease & clinical

No curated disease, variant, or cancer-driver associations.

Drugs & pharmacology

No drug or pharmacology data — not an established drug target.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): celiac disease, type 1 diabetes mellitus