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: SNX18 ENSBTAG00000027924

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Description

sorting nexin 18 [Source:VGNC Symbol;Acc:VGNC:35098]

Location

Primary_assembly 20: 24,483,654-24,575,118 reverse strand.

ARS-UCD2.0:CM008187.2

About this gene

This gene has 2 transcripts (splice variants), 270 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000040276.4	SNX18-202	4419	626aa	ENSBTAP00000040053.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A4IFN6	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,
ENSBTAT00000097266.1	SNX18-201	2118	599aa	ENSBTAP00000081261.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SBJ2	-

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Summary

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