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

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Gene: VWA2 ENSGALG00010022425

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Description

von Willebrand factor A domain containing 2 [Source:UniProtKB Gene Name;Acc:A0A8V0ZN90]

Location

Primary_assembly 6: 28,520,999-28,540,442 forward strand.

bGalGal1.mat.broiler.GRCg7b:CM028487.1

About this gene

This gene has 4 transcripts (splice variants), 178 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010054508.1	VWA2-201	2984	876aa	ENSGALP00010032924.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZN90	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 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,
ENSGALT00010054513.1	VWA2-202	3311	747aa	ENSGALP00010032928.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZVN6	-
ENSGALT00010054501.1	VWA2-204	2643	755aa	ENSGALP00010032919.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZN85	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,
ENSGALT00010054519.1	VWA2-203	2412	781aa	ENSGALP00010032932.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0ZHX5	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,

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Summary

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