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

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Gene: WSB2 ENSSSCG00000009853

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Description

WD repeat and SOCS box containing 2 [Source:VGNC Symbol;Acc:VGNC:94982]

Location

Primary_assembly 14: 34,609,075-34,632,269 forward strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 2 transcripts (splice variants), 206 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000010801.4	WSB2-201	4827	448aa	ENSSSCP00000010518.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1BI85 F1RKG3	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,
ENSSSCT00000081554.2	WSB2-202	4700	404aa	ENSSSCP00000067913.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2RBC9 A0A8D1J6M2	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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