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

Configure this page

Share this page

Bookmark this page

.

Gene: SNX29 ENSOCUG00000017079

.

Description

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

Location

Chromosome 6: 5,390,743-5,869,252 forward strand.

OryCun2.0:CM000795.1

About this gene

This gene has 3 transcripts (splice variants), 205 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000062033.1	SNX29-201	5465	1155aa	ENSOCUP00000040611.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSOCUT00000038686.1	SNX29-202	4934	978aa	ENSOCUP00000049613.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSOCUT00000017075.4	SNX29-203	3372	806aa	ENSOCUP00000014673.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1TCY5	-

.

Summary

.

.