Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: SNX22 ENSBTAG00000016821

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Description

sorting nexin 22 [Source:VGNC Symbol;Acc:VGNC:35102]

Location

Primary_assembly 10: 45,824,595-45,830,579 reverse strand.

ARS-UCD2.0:CM008177.2

About this gene

This gene has 2 transcripts (splice variants), 186 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000090140.1	SNX22-201	1466	221aa	ENSBTAP00000084288.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SK85	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,
ENSBTAT00000022377.6	SNX22-202	1194	183aa	ENSBTAP00000022377.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6RVQ5	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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