Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
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  - Gene tree
  - Orthologues
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Ontologies
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Genetic Variation
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ID History
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Gene: Gm16367 ENSMUSG00000096550

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Description

predicted gene 16367 [Source:NCBI gene (formerly Entrezgene);Acc:545762]

Location

Scaffold JH584299.1: 477,246-480,331 forward strand.

About this gene

This gene has 1 transcript (splice variant), 662 orthologues and 94 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000178337.2	Gm16367-201	1446	481aa	ENSMUSP00000136843.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q3UL49	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, 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,

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Summary

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