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: sfswap ENSDARG00000005980

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Description

splicing factor SWAP [Source:ZFIN;Acc:ZDB-GENE-040426-931]

Gene Synonyms

sfrs8, srsf8, zgc:56184

Location

Chromosome 21: 15,125,497-15,282,452 reverse strand.

GRCz11:CM002905.2

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000143113.3	sfswap-202	3660	958aa	ENSDARP00000121684.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q5L3	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,
ENSDART00000141809.2	sfswap-201	1206	276aa	ENSDARP00000115086.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1Q7E8	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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