Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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- Orthologues
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ID History
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Gene: 2610028H24Rik ENSMUSG00000009114

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Description

RIKEN cDNA 2610028H24 gene [Source:MGI Symbol;Acc:MGI:1924214]

Gene Synonyms

ORF67

Location

Chromosome 10: 76,284,915-76,296,944 forward strand.

GRCm39:CM001003.3

About this gene

This gene has 2 transcripts (splice variants) and 110 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000092406.12	2610028H24Rik-201	1640	270aa	ENSMUSP00000090061.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS35945	G5E8K1	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2, 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,
ENSMUST00000105415.3	2610028H24Rik-202	1464	249aa	ENSMUSP00000101055.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9Q7R5	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2, 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,

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Summary

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