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

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Gene: SNX3 ENSBTAG00000018801

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Description

sorting nexin 3 [Source:VGNC Symbol;Acc:VGNC:35107]

Location

Primary_assembly 9: 41,870,859-41,918,140 forward strand.

ARS-UCD2.0:CM008176.2

About this gene

This gene has 3 transcripts (splice variants), 223 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000119195.1	SNX3-202	1445	196aa	ENSBTAP00000095657.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9THG4	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,
ENSBTAT00000025026.5	SNX3-201	1363	162aa	ENSBTAP00000025026.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q1RMH8	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,
ENSBTAT00000102096.1	SNX3-203	1048	130aa	ENSBTAP00000079869.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SCA7	-

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Summary

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