Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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- Strains
  - Gene tree
  - Orthologues
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Ontologies
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ID History
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Gene: 4921517D22Rik ENSMUSG00000049902

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Description

RIKEN cDNA 4921517D22 gene [Source:MGI Symbol;Acc:MGI:1918150]

Location

Chromosome 13: 59,835,216-59,841,922 reverse strand.

GRCm39:CM001006.3

About this gene

This gene has 2 transcripts (splice variants) and 44 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000061597.7	4921517D22Rik-201	3149	269aa	ENSMUSP00000061773.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS36688	Q8CET0	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,
ENSMUST00000225373.2	4921517D22Rik-202	956	125aa	ENSMUSP00000153380.2	Nonsense mediated decay		A0A286YDE0	-

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Summary

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