Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
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ID History
- Gene history

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Gene: Dcun1d3 ENSRNOG00000066875

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Description

defective in cullin neddylation 1 domain containing 3 [Source:RGD Symbol;Acc:1308893]

Gene Synonyms

DCNL3, LOC309035, MGC114527, RGD1308893

Location

Primary_assembly 1: 183,678,548-183,717,002 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 1 transcript (splice variant), 225 orthologues and 5 paralogues.

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000019167.6	Dcun1d3-202	1473	304aa	ENSRNOP00000019167.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q9V9 A6I8P0 Q4V8B2	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 ALT1: 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 is conserved in at least 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 ALT1,

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Gene tree

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