country

Change Language

EN - English
FR - Français
DE - Deutsch
ES - Español
JA - 日本語
KO - 한국어

Product Name	Size / Unit Price	Qty

Total: USD 0.00 Checkout

VPS29 - VPS29 retromer complex component Gene

Also Known as DC7; DC15; PEP11

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 51699

About VPS29

Cytogenetic location: 12q24.11 Genomic coordinates (GRCh38): 12:110,491,083-110,502,111 (from NCBI)

This gene has 12 transcripts (splice variants) and 228 orthologues. Ubiquitous expression in fat (RPKM 31.1), esophagus (RPKM 28.7) and 25 other tissues.

Summary

This gene belongs to a group of vacuolar protein sorting (VPS) genes that, when functionally impaired, disrupt the efficient delivery of vacuolar hydrolases. The protein encoded by this gene is a component of a large multimeric complex, termed the retromer complex, which is involved in retrograde transport of proteins from endosomes to the trans-Golgi network. This VPS protein may be involved in the formation of the inner shell of the retromer coat for retrograde vesicles leaving the prevacuolar compartment. Alternative splice variants encoding different isoforms and representing non-protein coding transcripts have been found for this gene. [provided by RefSeq, Aug 2013]

VPS29 Products (4)

mRNA	Protein	Name
NM_001282150.2	NP_001269079.1	vacuolar protein sorting-associated protein 29 isoform 3
NM_001282151.2	NP_001269080.1	vacuolar protein sorting-associated protein 29 isoform 4
NM_016226.5	NP_057310.1	vacuolar protein sorting-associated protein 29 isoform 1
NM_057180.3	NP_476528.1	vacuolar protein sorting-associated protein 29 isoform 2

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	References	Source
enables protein binding	IPI IPI: Inferred from physical interaction	11102511	GOA

Biological Process GO Annotation	Evidence	References	Source
involved in endocytic recycling	IMP IMP: Inferred from mutant phenotype	28892079	GOA
NOT involved in regulation of autophagy	IMP IMP: Inferred from mutant phenotype	24603492	GOA

Cellular Component GO Annotation	Evidence	References	Source
located in cytosol	IDA IDA: Inferred from direct assay	11102511	GOA
part of retromer complex	IDA IDA: Inferred from direct assay	11102511	GOA
part of retromer, cargo-selective complex	IDA IDA: Inferred from direct assay	27385586	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

VPS29 Protein Structure

Metallophos_2

0
100
182 a.a.

Protein Preferred Names	Protein Names
vacuolar protein sorting-associated protein 29	PEP11 homolog

VPS29 Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	VPS29	Q9UBQ0	TBC1D5	Homo sapiens	B9A6K1	Y2H Prey Pooling	25416956
Intra	VPS29	Q9UBQ0	VPS26A	Homo sapiens	O75436	Anti Tag CoIP	17891154
Intra	VPS29	Q9UBQ0	VPS26A	Homo sapiens	O75436	Anti Tag CoIP	35271311
Intra	VPS29	Q9UBQ0	VPS26A	Homo sapiens	O75436	GMS	11102511
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	Anti Tag CoIP	35271311
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	Y2H Array	25502805
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	Anti Tag CoIP	37172566
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	ITC	24980502
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	GMS	17891154
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	Y2H Array	25416956
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	X-Ray Diffraction	17891154
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	Anti Tag CoIP	33961781
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	LexA B52 Complement	11102511
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	Anti Tag CoIP	17891154
Intra	VPS29	Q9UBQ0	VPS35	Homo sapiens	Q96QK1	Y2H Array	31515488
Intra	VPS29	Q9UBQ0	VPS35L	Homo sapiens	Q7Z3J2	Anti Tag CoIP	35271311
Intra	VPS29	Q9UBQ0	VPS35L	Homo sapiens	Q7Z3J2	Anti Tag CoIP	37172566
Intra	VPS29	Q9UBQ0	VPS35L	Homo sapiens	Q7Z3J2	ITC	37172566
Intra	VPS29	Q9UBQ0	VPS35L	Homo sapiens	Q7Z3J2	X-Ray Diffraction	37172566
Intra	VPS29	Q9UBQ0	VPS35L	Homo sapiens	Q7Z3J2	Anti Tag CoIP	33961781
Intra	VPS29	Q9UBQ0	VPS35L	Homo sapiens	Q7Z3J2	Pull Down	37172566
Intra	VPS29	Q9UBQ0	TBC1D5	Homo sapiens	Q92609	Anti Tag CoIP	35271311
Intra	VPS29	Q9UBQ0	TBC1D5	Homo sapiens	Q92609	Anti Tag CoIP	37172566
Intra	VPS29	Q9UBQ0	TBC1D5	Homo sapiens	Q92609	Anti Tag CoIP	24603492
Intra	VPS29	Q9UBQ0	TBC1D5	Homo sapiens	Q92609	Anti Tag CoIP	33961781

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases	Alias
Ritscher-Schinzel Syndrome	3c Syndrome Ccc Dysplasia Craniocerebellocardiac Dysplasia Cranio-Cerebello-Cardiac Dysplasia
Spastic Paraplegia 36, Autosomal Dominant	SPG36 Hereditary Spastic Paraplegia 36 Autosomal Dominant Spastic Paraplegia Type 36 Autosomal Dominant Spastic Paraplegia 36
Parkinson Disease, Late-Onset	Parkinson Disease Parkinson'S Disease PD PARK Parkinson Disease, Susceptibility To Late Onset Parkinson'S Disease Late Onset Parkinson Disease Paralysis Agitans Primary Parkinsonism Idiopathic Parkinson Disease Parkinson'S Parkinson Disease, Late-Onset, Susceptibility To Parkinson Disease, Age Of Onset, Modifier Lewy Body Parkinson Disease Idiopathic Parkinson'S Disease Pd - [Parkinson Disease] Parkinson Disease Nos Parkinson, Nos Primary Parkinson Disease
Legionnaire Disease	Legionnaires' Disease Legionnaires Disease Legionnaire Disease, Susceptibility To Legionella Legionella Pneumonia Infection By Legionella Pneumophilia Legionnaire'S Disease Legionellosis Legionaire Disease, Susceptibility To Legionnaires Pneumonia
Hereditary Spastic Paraplegia	Familial Spastic Paraplegia Hereditary Spastic Paraparesis Strumpell-Lorrain Disease Familial Spastic Paraparesis Hsp Spg Strümpell-Lorrain Disease Spastic Paraplegia, Hereditary French Settlement Disease Strumpell-Lorrain Syndrome Fsp Spastic Paraplegia, Familial Spastic Paraplegia Hereditary Spastic Paraplegia 3, Autosomal Dominant Spastic Paraparesis Hereditary Spastic Paralysis Familial Spastic Paralysis Hereditary Spastic Ataxia

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (3)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS15682	VPS29 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS22915	Vps29 Mouse Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS29429	Vps29 Rat Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Felis catus	VPS29	VGNC	VGNC:82553
Bos taurus	VPS29	VGNC	VGNC:36816
Canis familiaris	VPS29	VGNC	VGNC:48283
Rattus norvegicus	VPS29	RGD	RGD:1308332
Macaca mulatta	VPS29	VGNC	VGNC:78956
Mus musculus	VPS29	MGD	MGI:1928344
Others	VPS29	NCBI