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: cwc22 ENSDARG00000014008

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Description

CWC22 spliceosome associated protein homolog [Source:NCBI gene;Acc:566033]

Gene Synonyms

fb13g08, fi16b02, wu:fb13g08, wu:fi16b02, zgc:153452

Location

Chromosome 9: 43,552,515-43,644,261 reverse strand.

GRCz11:CM002893.2

About this gene

This gene has 2 transcripts (splice variants), 227 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000023684.10	cwc22-201	3295	983aa	ENSDARP00000013971.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0S6B1	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,
ENSDART00000136017.2	cwc22-202	877	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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