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

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Gene: WSCD2 ENSSSCG00000039261

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Description

WSC domain containing 2 [Source:VGNC Symbol;Acc:VGNC:109443]

Location

Primary_assembly 14: 42,489,398-42,584,135 reverse strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 2 transcripts (splice variants), 236 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000074194.2	WSCD2-202	2868	655aa	ENSSSCP00000070023.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QYS0 A0A8D1KZ95	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,
ENSSSCT00000063440.3	WSCD2-201	3547	564aa	ENSSSCP00000031913.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZKC8 A0A8D0M750	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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