Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Ctag2 ENSRNOG00000012560

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Description

cancer/testis antigen 2 [Source:RGD Symbol;Acc:1561702]

Gene Synonyms

LOC501655, RGD1561702

Location

Primary_assembly X: 148,567,674-148,568,968 forward strand.

GRCr8:CM070411.1

About this gene

This gene has 1 transcript (splice variant), 185 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000016754.5	Ctag2-201	789	199aa	ENSRNOP00000016754.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6K519 D3ZZR7	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 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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