Summary
- Splice variants
- Transcript comparison
- Gene alleles
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Comparative Genomics
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Ontologies
- GO: Anatomical entity
Phenotypes
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ID History
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Gene: 5730420D15Rik ENSMUSG00000097766

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Description

RIKEN cDNA 5730420D15 gene [Source:MGI Symbol;Acc:MGI:1917773]

Location

Chromosome 10: 95,252,845-95,279,547 forward strand.

GRCm39:CM001003.3

About this gene

This gene has 11 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	Flags
ENSMUST00000244592.1	5730420D15Rik-203	1132	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENSMUST00000301926.1	5730420D15Rik-204	1540	No protein	-	lncRNA		A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENSMUST00000181781.2	5730420D15Rik-201	1182	No protein	-	lncRNA		A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, 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,
ENSMUST00000301929.1	5730420D15Rik-207	1161	No protein	-	lncRNA		-
ENSMUST00000244160.1	5730420D15Rik-202	1024	No protein	-	lncRNA		-
ENSMUST00000301927.1	5730420D15Rik-205	1010	No protein	-	lncRNA		-
ENSMUST00000301928.1	5730420D15Rik-206	982	No protein	-	lncRNA		-
ENSMUST00000301931.1	5730420D15Rik-209	978	No protein	-	lncRNA		-
ENSMUST00000301930.1	5730420D15Rik-208	974	No protein	-	lncRNA		-
ENSMUST00000301933.1	5730420D15Rik-211	931	No protein	-	lncRNA		-
ENSMUST00000301932.1	5730420D15Rik-210	780	No protein	-	lncRNA		-

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Summary

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