Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Gene: 1700067P10Rik ENSMUSG00000021545

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Description

RIKEN cDNA 1700067P10 gene [Source:MGI Symbol;Acc:MGI:1915474]

Location

Chromosome 17: 48,399,839-48,401,438 forward strand.

GRCm39:CM001010.3

About this gene

This gene has 2 transcripts (splice variants) and 39 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000022028.6	1700067P10Rik-201	1105	183aa	ENSMUSP00000022028.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding		G3X8U2	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, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, 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,
ENSMUST00000233043.2	1700067P10Rik-202	1073	183aa	ENSMUSP00000156701.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		G3X8U2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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