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
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: WSCD2 ENSBTAG00000013686

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Description

WSC domain containing 2 [Source:VGNC Symbol;Acc:VGNC:36973]

Location

Primary_assembly 17: 64,604,374-64,657,774 reverse strand.

ARS-UCD1.3:CM008184.2

About this gene

This gene has 1 transcript (splice variant), 237 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000018189.5	WSCD2-201	2895	564aa	ENSBTAP00000018189.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MIR3	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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Summary

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