Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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  - Gene tree
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Ontologies
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Genetic Variation
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External references
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ID History
- Gene history

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Gene: Gm49721 ENSMUSG00000116876

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Description

predicted gene, 49721 [Source:MGI Symbol;Acc:MGI:6215195]

Location

Chromosome 17: 7,246,303-7,311,349 forward strand.

GRCm39:CM001010.3

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000231550.2	Gm49721-201	2610	259aa	ENSMUSP00000156290.2	Nonsense mediated decay	CCDS37429	C0HKG5 C0HKG6 Q5FWA0	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,

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Summary

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