Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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Ontologies
- GO: Anatomical entity
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Gene: Tex11 ENSRNOG00000025672

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Description

testis expressed 11 [Source:RGD Symbol;Acc:1560239]

Gene Synonyms

LOC501588, RGD1560239

Location

Primary_assembly X: 69,972,723-70,236,011 reverse strand.

GRCr8:CM070411.1

About this gene

This gene has 1 transcript (splice variant), 144 orthologues and is associated with 10 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000041731.8	Tex11-201	3578	946aa	ENSRNOP00000048393.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6M3WAI1 A0A9K3Y772 D3Z868	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,

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Summary

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