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

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Gene: SWSAP1 ENSBTAG00000008196

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Description

SWIM-type zinc finger 7 associated protein 1 [Source:VGNC Symbol;Acc:VGNC:35500]

Location

Primary_assembly 7: 15,772,765-15,776,715 forward strand.

ARS-UCD2.0:CM008174.2

About this gene

This gene has 2 transcripts (splice variants) and 101 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000131852.1	SWSAP1-202	1314	256aa	ENSBTAP00000089345.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SYK9	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000010778.6	SWSAP1-201	1950	249aa	ENSBTAP00000010778.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MER6	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Summary

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