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: Snx6 ENSRNOG00000005249

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Description

sorting nexin 6 [Source:RGD Symbol;Acc:1304647]

Gene Synonyms

LOC362738

Location

Primary_assembly 6: 72,229,870-72,315,911 reverse strand.

mRatBN7.2:CM026979.1

About this gene

This gene has 2 transcripts (splice variants), 223 orthologues, 16 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000117817.1	Snx6-202	2985	405aa	ENSRNOP00000081270.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZS69	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,
ENSRNOT00000007300.6	Snx6-201	1803	398aa	ENSRNOP00000007300.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7FPM8	-

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Summary

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