FALEC
gene geneOn this page
Also known as ncRNA-a1FAL1
Summary
FALEC (focally amplified lncRNA regulator of ECM1, HGNC:43713) is a long non-coding RNA gene on chromosome 1q21.2.
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:43713 |
| Approved symbol | FALEC |
| Name | focally amplified lncRNA regulator of ECM1 |
| Location | 1q21.2 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Aliases | ncRNA-a1, FAL1 |
| Ensembl gene | ENSG00000228126 |
| Ensembl biotype | lncRNA |
| OMIM | 616092 |
| Entrez | 100874054 |
| RNAcentral | URS00026A2707 — lncRNA, 741 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 9 — 9 lncRNA
ENST00000416894, ENST00000717990, ENST00000717991, ENST00000718312, ENST00000718313, ENST00000718314, ENST00000823964, ENST00000823965, ENST00000823966
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000416894 — 6 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001615428 | 150517773 | 150518120 |
| ENSE00001677463 | 150515752 | 150516062 |
| ENSE00004033839 | 150521333 | 150521405 |
| ENSE00004033841 | 150535667 | 150536788 |
| ENSE00004033844 | 150532657 | 150532786 |
| ENSE00004033846 | 150532250 | 150532393 |
Expression profiles
Bgee: expression breadth ubiquitous, 129 present calls, max score 92.18.
FANTOM5 (CAGE): breadth broad, TPM avg 0.6463 / max 28.1260, expressed in 324 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 5125 | 0.6463 | 324 |
Top tissues by expression
129 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| lower esophagus mucosa | UBERON:0035834 | 92.18 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 84.44 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 83.16 | gold quality |
| esophagus mucosa | UBERON:0002469 | 80.38 | gold quality |
| esophagus | UBERON:0001043 | 68.47 | gold quality |
| stromal cell of endometrium | CL:0002255 | 67.14 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 66.99 | gold quality |
| sural nerve | UBERON:0015488 | 66.29 | gold quality |
| cortical plate | UBERON:0005343 | 66.20 | gold quality |
| ventricular zone | UBERON:0003053 | 64.56 | gold quality |
| vagina | UBERON:0000996 | 64.35 | gold quality |
| prefrontal cortex | UBERON:0000451 | 62.96 | gold quality |
| apex of heart | UBERON:0002098 | 62.43 | gold quality |
| frontal cortex | UBERON:0001870 | 61.89 | gold quality |
| ganglionic eminence | UBERON:0004023 | 61.53 | gold quality |
| calcaneal tendon | UBERON:0003701 | 61.49 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 61.21 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 61.17 | gold quality |
| cerebellum | UBERON:0002037 | 61.01 | gold quality |
| cerebellar cortex | UBERON:0002129 | 60.93 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 60.92 | gold quality |
| ectocervix | UBERON:0012249 | 60.85 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 60.81 | gold quality |
| cerebral cortex | UBERON:0000956 | 60.76 | gold quality |
| right frontal lobe | UBERON:0002810 | 60.36 | gold quality |
| nucleus accumbens | UBERON:0001882 | 60.28 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 60.19 | gold quality |
| brain | UBERON:0000955 | 59.89 | gold quality |
| muscle of leg | UBERON:0001383 | 59.86 | gold quality |
| islet of Langerhans | UBERON:0000006 | 59.73 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.20 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 21)
- FAL1 associates with the epigenetic repressor BMI1 and regulates its stability in order to modulate the transcription of a number of genes including CDKN1A. (PMID:25203321)
- Its oncogenic activity is partially due to its repression of p21. and it may be a potential target for HCC therapy. (PMID:27154519)
- FALEC may promote the progression of Prostate cancer and be a potential diagnostic and therapeutic target in patients with Prostate cancer. (PMID:28585762)
- Overexpression of FAL1 facilitated tumor growth and metastasis by downregulating the PTEN/AKT signaling axis via BMI1. (PMID:28854421)
- this study indicated that lncRNA FAL1 functions as an oncogenic in hepatocellular carcinoma (HCC) and may be a novel diagnostic biomarker or a novel target for the treatment of HCC in future. (PMID:29421439)
- FAL1 expression was significantly upregulated in human osteosarcoma tissues and cell lines compared with their normal controls. lncRNA FAL1 exhibits an important pro-oncogenic effect on osteosarcoma progression by targeting epithelial-mesenchymal transition, which may serve as a potential therapeutic target for osteosarcoma. (PMID:29987852)
- lncRNA FAL1 promotes carcinogenesis of CRC cells via regulation of the miR-637/NUPR1 pathway. (PMID:30267804)
- High FAL1 expression is associated with colon cancer. (PMID:30290064)
- Highly expressed FAL1 can promote proliferation and migration of endothelial cells through activating PTEN/AKT signaling pathway in diabetic atherosclerosis. (PMID:30338819)
- Long non-coding RNA FAL1 regulates apoptosis of esophageal cancer cells via DRP1 and mitochondrial dynamics. (PMID:30501006)
- The overexpression of FAL1 regulates cell proliferation and cell cycle in gastric cancer cells by inhibiting PTEN. (PMID:30556865)
- FALEC was a potential molecular marker used to diagnose cervical cancer and evaluate prognosis (PMID:31248657)
- LncRNA FAL1 promotes the development of oral squamous cell carcinoma through regulating the microRNA-761/CRKL pathway. (PMID:31298329)
- The focally amplified long non-coding RNA in epithelial cancer (FALEC) was found downregulated in the tissues of tongue squamous cell carcinoma (TSCC) and was predicted to present a good prognosis by bioinformatics analysis. The data revealed that FALEC acted as a tumor suppressor in TSCC and may aid in developing a novel potential therapeutic strategy against TSCC. (PMID:31335317)
- FALEC is overexpressed in endometrial cancer tissues and cells, and involved in regulating cell proliferation and cell-cycle. (PMID:31387003)
- LncRNA FALEC promotes proliferation, migration, and invasion of PTC cells through regulating Wnt/beta-catenin signaling pathway. (PMID:32373973)
- Long non-coding RNA FALEC promotes colorectal cancer progression via regulating miR-2116-3p-targeted PIWIL1. (PMID:33073675)
- LncFALEC recruits ART5/PARP1 and promotes castration-resistant prostate cancer through enhancing PARP1-meditated self PARylation. (PMID:36913068)
- Extracellular vesicular lncRNA FAL1 promotes hepatocellular carcinoma cell proliferation and invasion by inducing macrophage M2 polarization. (PMID:37147492)
- LncRNA FALEC increases the proliferation, migration and drug resistance of cholangiocarcinoma through competitive regulation of miR-20a-5p/SHOC2 axis. (PMID:37166421)
- CAF-derived exosomal lncRNA FAL1 promotes chemoresistance to oxaliplatin by regulating autophagy in colorectal cancer. (PMID:37400281)
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
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.