Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: WNT2 ENSSSCG00000016628

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Description

Wnt family member 2 [Source:VGNC Symbol;Acc:VGNC:94968]

Location

Primary_assembly 18: 28,946,326-28,993,961 forward strand.

Sscrofa11.1:CM000829.5

About this gene

This gene has 1 transcript (splice variant), 208 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000045753.2	WNT2-201	5775	360aa	ENSSSCP00000051493.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287B4Y7 A0A8D0TY96	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,

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Paralogues

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Personal Data