Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: DCUN1D4 ENSBTAG00000001600

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Description

defective in cullin neddylation 1 domain containing 4 [Source:VGNC Symbol;Acc:VGNC:53698]

Location

Primary_assembly 6: 67,700,449-67,786,559 forward strand.

ARS-UCD1.3:CM008173.2

About this gene

This gene has 5 transcripts (splice variants), 211 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000131871.1	DCUN1D4-202	1502	397aa	ENSBTAP00000093523.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000122920.1	DCUN1D4-201	2070	289aa	ENSBTAP00000075669.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000073297.2	DCUN1D4-204	2000	332aa	ENSBTAP00000061808.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LP25	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,
ENSBTAT00000079725.2	DCUN1D4-203	1911	257aa	ENSBTAP00000068328.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MC18	-
ENSBTAT00000002106.5	DCUN1D4-205	552	183aa	ENSBTAP00000002106.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q32KS5	-

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Summary

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