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: ARNTL2 ENSBTAG00000011804

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Description

aryl hydrocarbon receptor nuclear translocator like 2 [Source:VGNC Symbol;Acc:VGNC:49075]

Location

Primary_assembly 5: 82,468,954-82,557,896 reverse strand.

ARS-UCD1.3:CM008172.2

About this gene

This gene has 4 transcripts (splice variants), 246 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000118136.1	ARNTL2-202	3038	635aa	ENSBTAP00000093479.1	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, 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,
ENSBTAT00000107466.1	ARNTL2-203	2996	621aa	ENSBTAP00000075616.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000126467.1	ARNTL2-201	2964	586aa	ENSBTAP00000079075.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000043261.4	ARNTL2-204	2936	601aa	ENSBTAP00000040847.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N4Q7	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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