LINC00467

gene
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Also known as MGC14801ASAP

Summary

LINC00467 (long intergenic non-protein coding RNA 467, HGNC:28227) is a long non-coding RNA gene on chromosome 1q32.3.

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:28227
Approved symbolLINC00467
Namelong intergenic non-protein coding RNA 467
Location1q32.3
Locus typeRNA, long non-coding
StatusApproved
AliasesMGC14801, ASAP
Ensembl geneENSG00000153363
Ensembl biotypelncRNA
OMIM620079
Entrez84791
RNAcentralURS000075ACB7 — lncRNA, 797 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 33 — 33 lncRNA

ENST00000423222, ENST00000448567, ENST00000534914, ENST00000610948, ENST00000653287, ENST00000653498, ENST00000653721, ENST00000654699, ENST00000654903, ENST00000656082, ENST00000656159, ENST00000656886, ENST00000657539, ENST00000659698, ENST00000660130, ENST00000660843, ENST00000661331, ENST00000662409, ENST00000662549, ENST00000663427, ENST00000663693, ENST00000664255, ENST00000665802, ENST00000666134, ENST00000667464, ENST00000669618, ENST00000670353, ENST00000689408, ENST00000703046, ENST00000818500, ENST00000818501, ENST00000818502, ENST00000818503

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000423222 — 6 exons

ExonStartEnd
ENSE00001794767211426211211426283
ENSE00003729521211391827211391976
ENSE00003730834211396767211396831
ENSE00003734384211391616211391697
ENSE00004222552211382727211382925
ENSE00004222559211432319211435333

Expression profiles

Bgee: expression breadth ubiquitous, 236 present calls, max score 99.67.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 13.7135 / max 569.7203, expressed in 1792 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
842513.71351792

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
spermCL:000001999.67gold quality
left testisUBERON:000453399.45gold quality
right testisUBERON:000453499.28gold quality
testisUBERON:000047397.55gold quality
adult organismUBERON:000702397.06gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047391.63gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099189.56gold quality
corpus epididymisUBERON:000435987.39gold quality
islet of LangerhansUBERON:000000687.25gold quality
sural nerveUBERON:001548886.78gold quality
caput epididymisUBERON:000435885.71gold quality
epithelial cell of pancreasCL:000008384.32silver quality
adrenal tissueUBERON:001830384.08gold quality
right adrenal glandUBERON:000123383.99gold quality
right adrenal gland cortexUBERON:003582783.93gold quality
left adrenal glandUBERON:000123483.66gold quality
left adrenal gland cortexUBERON:003582583.30gold quality
pancreasUBERON:000126483.27gold quality
adrenal glandUBERON:000236982.92gold quality
right lobe of liverUBERON:000111482.75gold quality
adrenal cortexUBERON:000123582.57gold quality
calcaneal tendonUBERON:000370182.57gold quality
bronchial epithelial cellCL:000232882.49gold quality
metanephros cortexUBERON:001053382.44gold quality
endothelial cellCL:000011582.18gold quality
body of pancreasUBERON:000115082.04gold quality
liverUBERON:000210781.76gold quality
bronchusUBERON:000218581.47gold quality
cauda epididymisUBERON:000436081.28gold quality
right uterine tubeUBERON:000130281.15gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes9.33

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 27)

  • N-Myc-mediated suppression of linc00467 gene transcription counterintuitively blocks N-Myc-mediated reduction in RD3 mRNA expression, and reduces neuroblastoma cell survival by inducing DKK1 expression (PMID:24586304)
  • LINC00467 epigenetically silenced DKK1 by recruiting enhancer of zeste 2 polycomb repressive complex 2 subunit (EZH2) to DKK1 promoter. (PMID:31027730)
  • LINC00467 expression was upregulated in human lung tumour tissues compared with normal tissues. (PMID:31180543)
  • LINC00467 silencing or miR-107 up-regulation repressed tumorigenic ability in xenograft tumor-bearing nude mice in cervical cancer in vivo. LINC00467 silencing or miR-107 up-regulation may serve as novel potential strategies for the treatment of cervical cancer. (PMID:31640853)
  • LINC00467 promotes cell proliferation and metastasis by binding with IGF2BP3 to enhance the mRNA stability of TRAF5 in hepatocellular carcinoma. (PMID:31656043)
  • Ferritin Light Chain (FTL) competes with long noncoding RNA Linc00467 for miR-133b binding site to regulate chemoresistance and metastasis of colorectal cancer. (PMID:31675755)
  • Long noncoding RNA linc00467 plays an oncogenic role in hepatocellular carcinoma by regulating the miR-18a-5p/NEDD9 axis. (PMID:31916278)
  • LINC00467 promotes proliferation and invasion in glioma via interacting with miRNA-485-5p. (PMID:32016980)
  • Long non-coding RNA LINC00467 drives hepatocellular carcinoma progression via inhibiting NR4A3. (PMID:32125766)
  • LINC00467 enhances head and neck squamous cell carcinoma progression and the epithelial-mesenchymal transition process via miR-299-5p/ubiquitin specific protease-48 axis. (PMID:32159247)
  • LINC00467 knockdown repressed cell proliferation but stimulated cell apoptosis in glioblastoma via miR-339-3p/IP6K2 axis. (PMID:32176627)
  • Knockdown of LINC00467 contributed to Axitinib sensitivity in hepatocellular carcinoma through miR-509-3p/PDGFRA axis. (PMID:32221502)
  • The Rs12569232 SNP Association with Vogt-Koyanagi-Harada Disease and Behcet’s Disease is Probably Mediated by Regulation of Linc00467 Expression. (PMID:32400232)
  • LncRNA LINC00467 contributes to osteosarcoma growth and metastasis through regulating HMGA1 by directly targeting miR-217. (PMID:32572906)
  • reveals the biological function of linc00467 to promote the resistance to adriamycin in acute myeloid leukemia (PMID:32669170)
  • Knockdown of long non-coding RNA LINC00467 inhibits glioma cell progression via modulation of E2F3 targeted by miR-200a. (PMID:32684096)
  • LncRNA LINC00467 acted as an oncogene in esophageal squamous cell carcinoma by accelerating cell proliferation and preventing cell apoptosis via the miR-485-5p/DPAGT1 axis. (PMID:32720371)
  • LINC00467 facilitates osteosarcoma progression by sponging miR217 to regulate KPNA4 expression. (PMID:33537823)
  • Overexpressed LINC00467 promotes the viability and proliferation yet inhibits apoptosis of gastric cancer cells via raising ITGB3 level. (PMID:34555778)
  • Micropeptide ASAP encoded by LINC00467 promotes colorectal cancer progression by directly modulating ATP synthase activity. (PMID:34591791)
  • Linc00467 promotion of gastric cancer development by directly regulating miR-7-5p expression and downstream epidermal growth factor receptor. (PMID:34713767)
  • LINC00467 Is Upregulated by DNA Copy Number Amplification and Hypomethylation and Shows ceRNA Potential in Lung Adenocarcinoma. (PMID:35095769)
  • LINC00467 facilitates the proliferation, migration and invasion of glioma via promoting the expression of inositol hexakisphosphate kinase 2 by binding to miR-339-3p. (PMID:35156508)
  • Downregulated Reprimo by LINC00467 participates in the growth and metastasis of gastric cancer. (PMID:35549646)
  • Silencing of LINC00467 inhibits cell proliferation in testicular germ cell tumors cells. (PMID:37078359)
  • LINC00467 mediates the 5-fluorouracil resistance in breast cancer cells. (PMID:38127229)
  • LINC00467 enhanced the proliferative, migratory and invasive ability of breast cancer cells by targeting miR-18a/b-5p/MAPK4 axis. (PMID:38279470)

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.