Summary
- Splice variants
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- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
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Molecular interactions
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ID History
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Gene: T2 ENSRNOG00000024172

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Description

brachyury 2 [Source:RGD Symbol;Acc:1597985]

Gene Synonyms

LOC681288

Location

Primary_assembly 1: 54,866,023-54,932,332 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 1 transcript (splice variant) and 11 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000033685.7	T2-201	1785	378aa	ENSRNOP00000032854.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LXU5	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, APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,

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Gene tree

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