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: ANGEL2 ENSSSCG00000015588

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Description

angel homolog 2 [Source:VGNC Symbol;Acc:VGNC:85302]

Location

Primary_assembly 9: 130,453,920-130,474,921 forward strand.

Sscrofa11.1:CM000820.5

About this gene

This gene has 4 transcripts (splice variants), 208 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000042646.2	ANGEL2-204	5531	544aa	ENSSSCP00000050701.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287B2R2 A0A4X1TP35	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSSSCT00000049420.3	ANGEL2-203	5093	341aa	ENSSSCP00000045354.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AMX3 A0A8D0STI6	-
ENSSSCT00000016981.4	ANGEL2-202	2637	530aa	ENSSSCP00000016527.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1VTP8 F1S2X8	-
ENSSSCT00000038645.3	ANGEL2-201	2280	418aa	ENSSSCP00000054312.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BDZ0 A0A4X1TP58	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,

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Summary

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