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: Snx8 ENSRNOG00000001258

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Description

sorting nexin 8 [Source:RGD Symbol;Acc:1305791]

Gene Synonyms

LOC288504

Location

Primary_assembly 12: 14,251,859-14,300,432 forward strand.

mRatBN7.2:CM026985.1

About this gene

This gene has 2 transcripts (splice variants), 219 orthologues, 16 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000001696.4	Snx8-201	2617	463aa	ENSRNOP00000001696.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZUJ9	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,
ENSRNOT00000110016.1	Snx8-202	2331	384aa	ENSRNOP00000087776.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A8L9	-

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Summary

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