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

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Gene: SNX33 ENSBTAG00000012206

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Description

sorting nexin 33 [Source:VGNC Symbol;Acc:VGNC:35110]

Location

Primary_assembly 21: 33,232,692-33,242,125 reverse strand.

ARS-UCD1.3:CM008188.2

About this gene

This gene has 2 transcripts (splice variants), 203 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000109296.1	SNX33-201	2961	586aa	ENSBTAP00000099605.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBTAT00000016186.4	SNX33-202	2193	571aa	ENSBTAP00000016186.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BHK6	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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