Summary
- Splice variants
- Transcript comparison
- Gene alleles
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Gene: Gm28778 ENSMUSG00000100679

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Description

predicted gene 28778 [Source:MGI Symbol;Acc:MGI:5579484]

Location

Chromosome 1: 53,336,270-53,365,502 forward strand.

GRCm39:CM000994.3

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000190734.3	Gm28778-201	1675	529aa	ENSMUSP00000141087.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A087WSK7	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 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,
ENSMUST00000249259.1	Gm28778-202	2147	136aa	ENSMUSP00000159639.1	Nonsense mediated decay		A0A9L6KDX5	-

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Summary

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