Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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- Gene gain/loss tree
- Orthologues
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  - Gene tree
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Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
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Pathway
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ID History
- Gene history

Gene: Cuedc2 ENSRNOG00000019574

Description

CUE domain containing 2 [Source:RGD Symbol;Acc:1308096]

Gene Synonyms

LOC294009, MGC156734

Location

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants) and 187 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000097448.2	Cuedc2-202	1176	316aa	ENSRNOP00000080530.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZQ90	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000026609.8	Cuedc2-201	1580	270aa	ENSRNOP00000026609.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2UK80	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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