Summary
- Splice variants
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Gene: 2700054A10Rik ENSMUSG00000117042

Description

RIKEN cDNA 2700054A10 gene [Source:MGI Symbol;Acc:MGI:1919828]

Location

Chromosome 17: 13,702,815-13,889,153 reverse strand.

GRCm39:CM001010.3

About this gene

This gene has 3 transcripts (splice variants) and is associated with 9 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSMUST00000137459.8	2700054A10Rik-201	4453	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, 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,
ENSMUST00000185626.7	2700054A10Rik-203	2213	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,
ENSMUST00000138345.8	2700054A10Rik-202	796	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,

Gene: 2700054A10Rik ENSMUSG00000117042

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Gene: 2700054A10Rik ENSMUSG00000117042

Summary

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