MEG8
gene geneOn this page
Also known as NCRNA00024IrmRianBsrLINC00024AL132709.8lnc-MGC
Summary
MEG8 (maternally expressed 8, small nucleolar RNA host gene, HGNC:14574) is a long non-coding RNA gene on chromosome 14q32.31.
This gene is located in a cluster of imprinted genes on chromosome 14q32.3. It encodes a a non-protein coding transcript that is preferentially expressed from the maternal allele in skeletal muscle, and appears to be coordinately regulated with other imprinted genes in this region.
Source: NCBI Gene 79104 — 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
| Field | Value |
|---|---|
| HGNC ID | HGNC:14574 |
| Approved symbol | MEG8 |
| Name | maternally expressed 8, small nucleolar RNA host gene |
| Location | 14q32.31 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Aliases | NCRNA00024, Irm, Rian, Bsr, LINC00024, AL132709.8, lnc-MGC |
| Ensembl gene | ENSG00000225746 |
| Ensembl biotype | lncRNA |
| OMIM | 613648 |
| Entrez | 79104 |
| RNAcentral | URS0000EEDA45 — lncRNA, 5564 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 65 — 65 lncRNA
ENST00000414488, ENST00000423708, ENST00000427085, ENST00000434716, ENST00000442197, ENST00000443252, ENST00000553421, ENST00000553465, ENST00000553584, ENST00000554323, ENST00000554369, ENST00000554485, ENST00000554693, ENST00000554852, ENST00000555354, ENST00000556475, ENST00000556637, ENST00000556720, ENST00000636052, ENST00000636391, ENST00000637332, ENST00000638012, ENST00000648818, ENST00000649300, ENST00000653102, ENST00000654340, ENST00000655773, ENST00000656987, ENST00000657772, ENST00000658511, ENST00000660698, ENST00000661496, ENST00000661815, ENST00000662228, ENST00000662832, ENST00000663218, ENST00000664819, ENST00000665015, ENST00000665480, ENST00000665787, ENST00000666001, ENST00000666972, ENST00000667813, ENST00000667814, ENST00000668102, ENST00000668545, ENST00000668595, ENST00000668725, ENST00000669238, ENST00000670454, ENST00000670680, ENST00000670877, ENST00000699458, ENST00000699459, ENST00000741820, ENST00000741821, ENST00000741822, ENST00000741823, ENST00000741824, ENST00000741825, ENST00000741826, ENST00000741827, ENST00000741828, ENST00000789029, ENST00000789030
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000414488 — 8 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001602356 | 100958262 | 100958550 |
| ENSE00003976622 | 100953964 | 100954046 |
| ENSE00003976623 | 100954922 | 100955006 |
| ENSE00003976626 | 100950402 | 100950472 |
| ENSE00003976629 | 100951432 | 100951494 |
| ENSE00003976631 | 100949515 | 100949596 |
| ENSE00003976634 | 100948978 | 100949039 |
| ENSE00004079349 | 100955885 | 100955949 |
Expression profiles
Bgee: expression breadth ubiquitous, 163 present calls, max score 99.63.
FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.3559 / max 35.1756, expressed in 160 samples.
FANTOM5 promoters (3 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 141570 | 0.2328 | 103 |
| 141573 | 0.0987 | 32 |
| 141565 | 0.0244 | 10 |
Top tissues by expression
247 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| adrenal tissue | UBERON:0018303 | 99.63 | gold quality |
| calcaneal tendon | UBERON:0003701 | 97.99 | gold quality |
| adenohypophysis | UBERON:0002196 | 94.75 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 93.81 | gold quality |
| pituitary gland | UBERON:0000007 | 93.00 | gold quality |
| sural nerve | UBERON:0015488 | 92.05 | gold quality |
| right adrenal gland | UBERON:0001233 | 90.26 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 89.93 | gold quality |
| left ovary | UBERON:0002119 | 89.92 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 89.87 | gold quality |
| left adrenal gland | UBERON:0001234 | 89.03 | gold quality |
| adrenal cortex | UBERON:0001235 | 88.05 | gold quality |
| adrenal gland | UBERON:0002369 | 88.05 | gold quality |
| tendon | UBERON:0000043 | 87.90 | gold quality |
| hypothalamus | UBERON:0001898 | 87.64 | gold quality |
| right ovary | UBERON:0002118 | 87.55 | gold quality |
| colonic epithelium | UBERON:0000397 | 86.92 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 85.77 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 85.27 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 85.24 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 84.36 | gold quality |
| cerebellar cortex | UBERON:0002129 | 84.34 | gold quality |
| right frontal lobe | UBERON:0002810 | 84.32 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 83.80 | gold quality |
| nucleus accumbens | UBERON:0001882 | 83.22 | gold quality |
| amygdala | UBERON:0001876 | 82.82 | gold quality |
| ovary | UBERON:0000992 | 82.78 | gold quality |
| cerebellum | UBERON:0002037 | 82.25 | gold quality |
| stromal cell of endometrium | CL:0002255 | 81.74 | gold quality |
| body of pancreas | UBERON:0001150 | 80.55 | gold quality |
Single-cell (SCXA)
Detected in 2 experiment(s), a significant marker in 2.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 18.26 |
| E-HCAD-25 | yes | 7.86 |
Regulation
Is transcription factor: no
Upstream regulators (CollecTRI, top): NEUROG2
Literature-anchored findings (GeneRIF, showing 16)
- MEG8, located in a cluster of imprinted genes on chromosome 14q32.3, is preferentially expressed from the maternal allele. (PMID:11337479)
- MEG8-DMR is hypermethylated in each of 13 non-deletion Temple syndrome patients. (PMID:28635951)
- Endogenous MEG8 lncRNA is indispensable for TGF-beta-induced epithelial-mesenchymal transition in A549 lung cancer and Panc1 pancreatic cancer cells. (PMID:30262664)
- MEG8 regulates the proliferation and migration of VSMCs via the MEG8/miR-181a/PPARalpha axis. (PMID:30670309)
- Meg8 suppresses hepatic stellate cells activation and hepatocyte epithelial-mesenchymal transition through inhibiting the Notch pathway. (PMID:31711641)
- LncRNA MEG8 promotes tumor progression of non-small cell lung cancer via regulating miR-107/CDK6 axis. (PMID:32649368)
- LncRNA MEG8 plays an oncogenic role in hepatocellular carcinoma progression through miR-367-3p/14-3-3zeta/TGFbetaR1 axis. (PMID:33147050)
- LncRNA MEG8 is upregulated in gestational diabetes mellitus (GDM) and predicted kidney injury. (PMID:33189541)
- Identification of MEG8/miR-378d/SOBP axis as a novel regulatory network and associated with immune infiltrates in ovarian carcinoma by integrated bioinformatics analysis. (PMID:33742531)
- Silencing long non-coding RNA MEG8 inhibits the proliferation and induces the ferroptosis of hemangioma endothelial cells by regulating miR-497-5p/NOTCH2 axis. (PMID:33839417)
- LncRNA MEG8 promotes TNF-alpha expression by sponging miR-454-3p in bone-invasive pituitary adenomas. (PMID:34016788)
- Silencing of lncRNA MEG8 Represses the Viability, Migration, and Invasion of Wilms’ Tumor Cells through Mediating miR-23a-3p/CRK Axis. (PMID:34518485)
- Knockdown of lncRNA MEG8 inhibits cell proliferation and invasion, but promotes cell apoptosis in hemangioma, via miR203induced mediation of the Notch signaling pathway. (PMID:34713294)
- MEG8 regulates Tissue Factor Pathway Inhibitor 2 (TFPI2) expression in the endothelium. (PMID:35039572)
- MEG8: An Indispensable Long Non-coding RNA in Multiple Cancers. (PMID:35578848)
- LncRNA MEG8 ameliorates Parkinson’s disease neuro-inflammation through miR-485-3p/FBXO45 axis. (PMID:37814093)
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.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): specific language impairment