Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Comparative Genomics
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Genetic Variation
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Gene: 1700003E16Rik ENSMUSG00000030030

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Description

RIKEN cDNA 1700003E16 gene [Source:MGI Symbol;Acc:MGI:1919087]

Location

Chromosome 6: 83,133,386-83,139,927 forward strand.

GRCm39:CM000999.3

About this gene

This gene has 2 transcripts (splice variants) and 81 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000032106.6	1700003E16Rik-201	2020	598aa	ENSMUSP00000032106.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS51818	Q9DAQ4	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 5: A transcript where no single transcript supports the model structure. 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:5,
ENSMUST00000203203.2	1700003E16Rik-202	2070	113aa	ENSMUSP00000145406.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A0N4SW77	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs 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:2,

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Summary

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