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

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Gene: SNX13 ENSSSCG00000024761

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Description

sorting nexin 13 [Source:VGNC Symbol;Acc:VGNC:93306]

Location

Primary_assembly 9: 86,964,045-87,086,577 reverse strand.

Sscrofa11.1:CM000820.5

About this gene

This gene has 2 transcripts (splice variants), 217 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000029645.4	SNX13-202	6279	957aa	ENSSSCP00000027899.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3LUU8	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,
ENSSSCT00000048803.3	SNX13-201	7104	888aa	ENSSSCP00000041852.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AD08 A0A8D0ZUS5	-

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Paralogues

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