Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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: VWDE ENSPTRG00000018938

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Description

von Willebrand factor D and EGF domains [Source:VGNC Symbol;Acc:VGNC:4562]

Location

Chromosome 7: 11,351,597-11,438,480 reverse strand.

Pan_tro_3.0:CM000321.4

About this gene

This gene has 3 transcripts (splice variants), 129 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000035011.5	VWDE-201	4773	1591aa	ENSPTRP00000032356.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2QU72	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,
ENSPTRT00000108402.1	VWDE-203	3909	1302aa	ENSPTRP00000092730.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TTY0	-
ENSPTRT00000078096.1	VWDE-202	2799	932aa	ENSPTRP00000069810.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RYK5	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,

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Summary

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