Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Snx31 ENSRNOG00000025501

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Description

sorting nexin 31 [Source:RGD Symbol;Acc:1309483]

Gene Synonyms

LOC366915, RGD1309483

Location

Primary_assembly 7: 69,553,205-69,617,396 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 115 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000135582.1	Snx31-202	1804	443aa	ENSRNOP00000105998.1	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,
ENSRNOT00000036852.7	Snx31-201	2628	439aa	ENSRNOP00000037890.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LZE2	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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