Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Snx13 ENSRNOG00000004186

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Description

sorting nexin 13 [Source:RGD Symbol;Acc:1309778]

Gene Synonyms

LOC362731

Location

Primary_assembly 6: 57,434,273-57,589,624 forward strand.

GRCr8:CM070396.1

About this gene

This gene has 3 transcripts (splice variants), 214 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000095510.2	Snx13-203	6890	1144aa	ENSRNOP00000089422.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GI34	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,
ENSRNOT00000005637.7	Snx13-201	6820	1133aa	ENSRNOP00000005637.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZCH3	-
ENSRNOT00000084661.3	Snx13-202	4106	888aa	ENSRNOP00000069103.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JUH8	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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