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
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: snx30 ENSDARG00000069601

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Description

sorting nexin family member 30 [Source:NCBI gene;Acc:550496]

Gene Synonyms

zgc:112424

Location

Chromosome 10: 4,940,767-4,961,929 reverse strand.

GRCz11:CM002894.2

About this gene

This gene has 2 transcripts (splice variants), 202 orthologues and 20 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000050177.7	snx30-201	2017	430aa	ENSDARP00000050176.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QDU5	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,
ENSDART00000146066.2	snx30-202	896	260aa	ENSDARP00000116137.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E9QCF2	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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