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

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Gene: DUS3L ENSBTAG00000011842

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Description

dihydrouridine synthase 3 like [Source:VGNC Symbol;Acc:VGNC:103057]

Location

Primary_assembly 7: 18,541,354-18,546,806 forward strand.

ARS-UCD2.0:CM008174.2

About this gene

This gene has 4 transcripts (splice variants), 193 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000107129.1	DUS3L-201	2368	732aa	ENSBTAP00000090404.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SYG1	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,
ENSBTAT00000081362.2	DUS3L-203	2692	646aa	ENSBTAP00000066642.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M942	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,
ENSBTAT00000015715.7	DUS3L-204	2010	642aa	ENSBTAP00000015715.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BGZ1	-
ENSBTAT00000126856.1	DUS3L-202	1396	408aa	ENSBTAP00000074683.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RUE0	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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Summary

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