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: LINC00305 ENSG00000179676

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Description

long intergenic non-protein coding RNA 305 [Source:HGNC Symbol;Acc:HGNC:28597]

Gene Synonyms

C18ORF20, HST1235, MGC39571, NCRNA00305

Location

Chromosome 18: 64,079,989-64,149,088 reverse strand.

GRCh38:CM000680.2

About this gene

This gene has 16 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq Match	Flags
ENST00000666468.1	LINC00305-212	954	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,
ENST00000657385.1	LINC00305-204	1340	No protein	-	lncRNA		-	-
ENST00000671534.1	LINC00305-216	1333	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,
ENST00000669361.1	LINC00305-214	1240	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,
ENST00000658718.1	LINC00305-206	1087	No protein	-	lncRNA		-	-
ENST00000657912.1	LINC00305-205	969	No protein	-	lncRNA		-	-
ENST00000659895.1	LINC00305-207	890	No protein	-	lncRNA		-	-
ENST00000323355.3	LINC00305-201	873	No protein	-	lncRNA		-	TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. 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:1,
ENST00000663021.1	LINC00305-209	837	No protein	-	lncRNA		-	-
ENST00000665443.1	LINC00305-210	812	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,
ENST00000665461.1	LINC00305-211	796	No protein	-	lncRNA		-	-
ENST00000662600.1	LINC00305-208	713	No protein	-	lncRNA		-	-
ENST00000669878.1	LINC00305-215	559	No protein	-	lncRNA		-	-
ENST00000668958.1	LINC00305-213	431	No protein	-	lncRNA		-	-
ENST00000454647.1	LINC00305-202	339	No protein	-	lncRNA		-	TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. 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:1,
ENST00000456505.1	LINC00305-203	217	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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