Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Supporting evidence
ID History
- Gene history

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Gene: CWC15 ENSPTRG00000044239

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Description

CWC15 spliceosome associated protein homolog [Source:UniProtKB Gene Name;Acc:K7BH91]

Location

Chromosome 11: 95,037,871-95,048,665 reverse strand.

Pan_tro_3.0:CM000325.3

About this gene

This gene has 2 transcripts (splice variants) and 228 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000082872.1	CWC15-201	1262	229aa	ENSPTRP00000073392.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X9R1 K7BH91	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,
ENSPTRT00000098059.1	CWC15-202	1226	229aa	ENSPTRP00000082002.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X9R1 K7BH91	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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