Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: SNX29 ENSCPOG00000014559

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Description

sorting nexin 29 [Source:HGNC Symbol;Acc:HGNC:30542]

Location

Scaffold DS562859.1: 30,920,158-31,474,777 forward strand.

About this gene

This gene has 2 transcripts (splice variants), 205 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSCPOT00000024021.2	SNX29-201	2364	787aa	ENSCPOP00000017730.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H0W431	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,
ENSCPOT00000014704.3	SNX29-202	966	322aa	ENSCPOP00000013119.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H0VRB4	-

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Summary

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