Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Dcun1d1 ENSRNOG00000012734

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Description

defective in cullin neddylation 1 domain containing 1 [Source:RGD Symbol;Acc:1309668]

Gene Synonyms

LOC100912352, LOC102553014, LOC310324, Tes3

Location

Primary_assembly 2: 120,649,445-120,700,870 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 5 transcripts (splice variants), 230 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000104731.2	Dcun1d1-201	4581	274aa	ENSRNOP00000084408.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZYZ4	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,
ENSRNOT00000109045.2	Dcun1d1-203	4777	273aa	ENSRNOP00000090810.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ADB9	-
ENSRNOT00000104963.2	Dcun1d1-202	4750	264aa	ENSRNOP00000076537.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y621	-
ENSRNOT00000150607.1	Dcun1d1-205	4744	262aa	ENSRNOP00000110661.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000111905.2	Dcun1d1-204	4589	259aa	ENSRNOP00000092738.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AI94	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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