Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Vwc2 ENSRNOG00000049076

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Description

von Willebrand factor C domain containing 2 [Source:RGD Symbol;Acc:1589624]

Gene Synonyms

LOC501231

Location

Primary_assembly 14: 89,897,887-90,032,188 forward strand.

GRCr8:CM070404.1

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues and 21 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000147456.1	Vwc2-202	2698	361aa	ENSRNOP00000104336.1	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,
ENSRNOT00000071558.3	Vwc2-201	3364	324aa	ENSRNOP00000066776.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KJ97 M0RB53	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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