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

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Gene: LINC02266 ENSG00000272727

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Description

long intergenic non-protein coding RNA 2266 [Source:HGNC Symbol;Acc:HGNC:53180]

Location

Chromosome 4: 145,335,263-145,343,559 reverse strand.

GRCh38:CM000666.2

About this gene

This gene has 7 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq Match	Flags
ENST00000654926.1	LINC02266-202	1164	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,
ENST00000664112.1	LINC02266-206	1468	No protein	-	lncRNA		-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000659879.1	LINC02266-204	1364	No protein	-	lncRNA		-	-
ENST00000660722.1	LINC02266-205	1300	No protein	-	lncRNA		-	-
ENST00000667468.1	LINC02266-207	1217	No protein	-	lncRNA		-	-
ENST00000610239.2	LINC02266-201	1211	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,
ENST00000659559.1	LINC02266-203	1177	No protein	-	lncRNA		-	-

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Summary

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