LINCADL

gene
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Also known as linc-ADAL

Summary

LINCADL (lincRNA adipogenesis and lipogenesis associated, HGNC:53956) is a long non-coding RNA gene on chromosome 5q23.1.

This gene encodes a long noncoding RNA involved in adipocyte differentiation and fatty acid synthesis. Expression of this gene is enriched in human adipose tissue. The long noncoding RNA product of this gene has been shown to interact with cytoplasmic and nuclear proteins, and these interactions may be important in post-transcriptional regulation of lipid metabolism genes.

Source: NCBI Gene 107986443 — 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:53956
Approved symbolLINCADL
NamelincRNA adipogenesis and lipogenesis associated
Location5q23.1
Locus typeRNA, long non-coding
StatusApproved
Aliaseslinc-ADAL
Ensembl geneENSG00000287148
Ensembl biotypelncRNA
Entrez107986443
RNAcentralURS0000D780CF — lncRNA, 523 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 3 — 3 lncRNA

ENST00000666259, ENST00000723762, ENST00000723763

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000666259 — 2 exons

ExonStartEnd
ENSE00004045744115956530115956920
ENSE00004045747115958429115958604

Expression profiles

Bgee: expression breadth ubiquitous, 103 present calls, max score 97.66.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 1.2144 / max 227.6830, expressed in 66 samples.

FANTOM5 promoters (5 alternative TSS)

Promoter IDTPM avgSamples expressed
580550.441850
580520.374946
580530.295941
580540.078426
580510.023414

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
colonic epitheliumUBERON:000039797.66gold quality
subcutaneous adipose tissueUBERON:000219094.48gold quality
adipose tissueUBERON:000101393.59gold quality
omental fat padUBERON:001041492.36gold quality
thoracic mammary glandUBERON:000520085.74gold quality
hindlimb stylopod muscleUBERON:000425281.00gold quality
descending thoracic aortaUBERON:000234575.92gold quality
left coronary arteryUBERON:000162671.99gold quality
rectumUBERON:000105271.08gold quality
skeletal muscle tissueUBERON:000113468.04gold quality
muscle tissueUBERON:000238567.44gold quality
tibial nerveUBERON:000132364.65gold quality
lymph nodeUBERON:000002963.12gold quality
calcaneal tendonUBERON:000370162.55gold quality
right coronary arteryUBERON:000162561.65gold quality
sural nerveUBERON:001548861.57gold quality
urinary bladderUBERON:000125561.13gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099160.75gold quality
fundus of stomachUBERON:000116059.70gold quality
multicellular organismUBERON:000046859.69gold quality
vermiform appendixUBERON:000115459.63gold quality
monocyteCL:000057658.26gold quality
heartUBERON:000094857.54gold quality
muscle of legUBERON:000138356.42gold quality
skin of legUBERON:000151155.62gold quality
left ovaryUBERON:000211955.59gold quality
gastrocnemiusUBERON:000138855.50gold quality
saliva-secreting glandUBERON:000104455.12gold quality
right atrium auricular regionUBERON:000663155.09gold quality
ovaryUBERON:000099254.99gold quality

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • linc-ADAL interacts with heterogeneous nuclear ribonucleoprotein U (hnRNPU) and insulin-like growth factor 2 mRNA binding protein 2 (IGF2BP2) at distinct subcellular locations to regulate adipocyte differentiation and lipogenesis. (PMID:29925637)

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.