Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Dcun1d3 ENSRNOG00000014037

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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: 66,494,848-66,496,343 reverse strand.

mRatBN7.2:CM026974.1

About this gene

This gene has 1 transcript (splice variant), 227 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000116639.1	Dcun1d3-201	486	161aa	ENSRNOP00000090559.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ANH6	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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