Gene: VWF ENSSSCG00000063591

Description

von Willebrand factor [Source:NCBI gene (formerly Entrezgene);Acc:399543]

Location

Sscrofa11.1:CM000816.5

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues, 21 paralogues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000000775.6	VWF-201	8665	2807aa	ENSSSCP00000000759.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1SL22	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,
ENSSSCT00000036466.5	VWF-202	8448	353aa	ENSSSCP00000029485.4	Nonsense mediated decay	K7GNN0	-

Phenotypes