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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SNX29 ENSPANG00000014214

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Description

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

Location

Primary_assembly 18: 61,398,647-61,976,148 reverse strand.

Panubis1.0:CM018197.1

About this gene

This gene has 1 transcript (splice variant), 205 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPANT00000012350.4	SNX29-201	2451	816aa	ENSPANP00000013930.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096NLS2	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,

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Summary

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