Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- 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: LINC01622 ENSG00000286785

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Description

long intergenic non-protein coding RNA 1622 [Source:HGNC Symbol;Acc:HGNC:27768]

Gene Synonyms

TCONS_00011202

Location

Chromosome 6: 958,323-1,101,400 reverse strand.

GRCh38:CM000668.2

About this gene

This gene has 8 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq Match	Flags
ENST00000655659.1	LINC01622-202	2213	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,
ENST00000663447.1	LINC01622-205	2465	No protein	-	lncRNA		-	-
ENST00000662378.1	LINC01622-204	2396	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,
ENST00000661526.1	LINC01622-203	2135	No protein	-	lncRNA		-	-
ENST00000664781.1	LINC01622-206	2014	No protein	-	lncRNA		-	-
ENST00000668813.1	LINC01622-207	1945	No protein	-	lncRNA		-	-
ENST00000669177.1	LINC01622-208	1612	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,
ENST00000612554.2	LINC01622-201	1202	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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