Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: LINC02379 ENSG00000251649

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Description

long intergenic non-protein coding RNA 2379 [Source:HGNC Symbol;Acc:HGNC:53302]

Location

Chromosome 4: 126,064,128-126,073,370 forward strand.

GRCh38:CM000666.2

About this gene

This gene has 6 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq Match	Flags
ENST00000655624.1	LINC02379-202	1822	No protein	-	lncRNA		-	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000670367.1	LINC02379-206	1254	No protein	-	lncRNA		-	-
ENST00000657991.1	LINC02379-203	1135	No protein	-	lncRNA		-	-
ENST00000667815.1	LINC02379-205	791	No protein	-	lncRNA		-	-
ENST00000658298.1	LINC02379-204	598	No protein	-	lncRNA		-	-
ENST00000505741.2	LINC02379-201	552	No protein	-	lncRNA		-	TSL 3: A transcript where the only support is from a single EST The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:3,

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Summary

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