Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SNX32 ENSPTRG00000003894

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Description

sorting nexin 32 [Source:VGNC Symbol;Acc:VGNC:1001]

Location

Chromosome 11: 65,901,173-65,920,927 forward strand.

Pan_tro_3.0:CM000325.3

About this gene

This gene has 2 transcripts (splice variants), 155 orthologues and 17 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000083267.1	SNX32-202	1215	404aa	ENSPTRP00000086123.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TA96	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,
ENSPTRT00000007279.4	SNX32-201	2015	403aa	ENSPTRP00000006714.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XAV4 H2Q443	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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