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

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Gene: snx11 ENSDARG00000052522

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Description

sorting nexin 11 [Source:ZFIN;Acc:ZDB-GENE-041111-253]

Gene Synonyms

im:7148910, si:dkey-220f10.6, zgc:136459

Location

Chromosome 12: 20,605,191-20,616,160 reverse strand.

GRCz11:CM002896.2

About this gene

This gene has 1 transcript (splice variant), 206 orthologues and 20 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000105362.5	snx11-201	4211	506aa	ENSDARP00000096134.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R6M7	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,

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Summary

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