LINC00862

gene
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Summary

LINC00862 (long intergenic non-protein coding RNA 862, HGNC:21901) is a long non-coding RNA gene on chromosome 1q32.1.

Predicted to be located in membrane.

Source: NCBI Gene 554279 — 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:21901
Approved symbolLINC00862
Namelong intergenic non-protein coding RNA 862
Location1q32.1
Locus typeRNA, long non-coding
StatusApproved
Ensembl geneENSG00000203721
Ensembl biotypelncRNA
Entrez554279
RNAcentralURS000075D6D3 — lncRNA, 1445 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 33 — 33 lncRNA

ENST00000367355, ENST00000367356, ENST00000636153, ENST00000637098, ENST00000656731, ENST00000669359, ENST00000669708, ENST00000688178, ENST00000760608, ENST00000760609, ENST00000760610, ENST00000760611, ENST00000760612, ENST00000760613, ENST00000760614, ENST00000760615, ENST00000760616, ENST00000760617, ENST00000760618, ENST00000760619, ENST00000760620, ENST00000760621, ENST00000760622, ENST00000760623, ENST00000760624, ENST00000760625, ENST00000760626, ENST00000760627, ENST00000760628, ENST00000760629, ENST00000760630, ENST00000760631, ENST00000760632

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000367355 — 5 exons

ExonStartEnd
ENSE00001444306200342541200343410
ENSE00001444307200368665200368871
ENSE00001444308200371046200371165
ENSE00003701975200373093200373169
ENSE00004114405200373647200373840

Expression profiles

Bgee: expression breadth ubiquitous, 144 present calls, max score 76.07.

FANTOM5 (CAGE): breadth broad, TPM avg 0.6195 / max 52.5756, expressed in 214 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
165690.4930146
165680.126560

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047376.07gold quality
right lobe of liverUBERON:000111470.26gold quality
stromal cell of endometriumCL:000225566.32gold quality
sural nerveUBERON:001548865.44gold quality
bloodUBERON:000017864.23gold quality
spermCL:000001961.90gold quality
corpus callosumUBERON:000233661.64gold quality
liverUBERON:000210761.20gold quality
buccal mucosa cellCL:000233660.88gold quality
ganglionic eminenceUBERON:000402358.94gold quality
C1 segment of cervical spinal cordUBERON:000646958.46gold quality
cortical plateUBERON:000534358.29silver quality
spinal cordUBERON:000224056.80gold quality
spleenUBERON:000210655.30gold quality
putamenUBERON:000187454.22gold quality
prefrontal cortexUBERON:000045153.48gold quality
monocyteCL:000057653.38silver quality
mucosa of transverse colonUBERON:000499153.30gold quality
substantia nigraUBERON:000203853.02gold quality
tonsilUBERON:000237253.02gold quality
gall bladderUBERON:000211052.83gold quality
amygdalaUBERON:000187652.79gold quality
body of pancreasUBERON:000115052.14gold quality
calcaneal tendonUBERON:000370152.13silver quality
caudate nucleusUBERON:000187352.11gold quality
right lungUBERON:000216752.07gold quality
lymph nodeUBERON:000002951.88gold quality
muscle of legUBERON:000138351.71gold quality
minor salivary glandUBERON:000183051.52gold quality
pancreasUBERON:000126451.42gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.63

Regulation

Is transcription factor: no

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): refractive error