Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Molecular interactions
Regulation
External references
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ID History
- Gene history

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Gene: DTL ENSBTAG00000018142

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Description

denticleless E3 ubiquitin [Source:VGNC Symbol;Acc:VGNC:28230]

Location

Primary_assembly 16: 71,386,304-71,466,322 reverse strand.

ARS-UCD2.0:CM008183.2

About this gene

This gene has 3 transcripts (splice variants) and 206 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000074215.2	DTL-202	2806	720aa	ENSBTAP00000072712.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MLX1	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,
ENSBTAT00000024147.7	DTL-201	2372	718aa	ENSBTAP00000024147.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BJV8	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,
ENSBTAT00000066830.2	DTL-203	2079	688aa	ENSBTAP00000063590.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N2R3	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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