VBP1 - VHL binding protein 1 Gene

Also Known as PFD3; PFDN3; VBP-1; HIBBJ46

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7411

About VBP1

Cytogenetic location: Xq28 Genomic coordinates (GRCh38): X:155,197,007-155,239,841 (from NCBI)

This gene has 4 transcripts (splice variants) and 218 orthologues. Ubiquitous expression in brain (RPKM 27.3), heart (RPKM 18.7) and 25 other tissues.

Summary

The protein encoded by this gene interacts with the Von Hippel-Lindau protein to form an intracellular complex. The encoded protein functions as a chaperone protein, and may play a role in the transport of the Von Hippel-Lindau protein from the perinuclear granules to the nucleus or cytoplasm. Alternative splicing and the use of alternate transcription start sites results in multiple transcript variants encoding different protein isoforms. [provided by RefSeq, Jan 2015]

VBP1 Products (4)

mRNA Protein Name
NM_001303543.1 NP_001290472.1 prefoldin subunit 3 isoform 2
NM_001303544.1 NP_001290473.1 prefoldin subunit 3 isoform 3
NM_001303545.1 NP_001290474.1 prefoldin subunit 3 isoform 4
NM_003372.7 NP_003363.1 prefoldin subunit 3 isoform 1
Molecular Function GO Annotation Evidence References Source
enables amyloid-beta binding IDA
IDA: Inferred from direct assay
23614719 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17698809 GOA
enables unfolded protein binding IDA
IDA: Inferred from direct assay
30955883 GOA
Biological Process GO Annotation Evidence References Source
involved in negative regulation of amyloid fibril formation IDA
IDA: Inferred from direct assay
23614719 GOA
involved in protein folding IDA
IDA: Inferred from direct assay
30955883 GOA
Cellular Component GO Annotation Evidence References Source
part of prefoldin complex IDA
IDA: Inferred from direct assay
23614719 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

VBP1 Protein Structure

Prefoldin

Prefoldin: Prefoldin subunit (60 - 182)

  • 0
  • 100
  • 197 a.a.
Protein Preferred Names Protein Names

prefoldin subunit 3

  • von Hippel-Lindau binding protein 1

VBP1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
VBP1 P61758 SULT1B1 Homo sapiens O43704 32814053
Intra
VBP1 P61758 SULT1B1 Homo sapiens O43704 32814053
Intra
VBP1 P61758 SULT1B1 Homo sapiens O43704 32814053
Intra
VBP1 P61758 ZNF410 Homo sapiens Q86VK4-3 32296183
Intra
VBP1 P61758 LMO3 Homo sapiens Q8TAP4-4 32296183
Intra
VBP1 P61758 TCEANC Homo sapiens Q8N8B7-2 32296183
Intra
VBP1 P61758 VEZF1 Homo sapiens Q14119 32296183
Intra
VBP1 P61758 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
VBP1 P61758 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
VBP1 P61758 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
VBP1 P61758 THAP3 Homo sapiens Q8WTV1 32814053
Intra
VBP1 P61758 THAP3 Homo sapiens Q8WTV1 32814053
Intra
VBP1 P61758 THAP3 Homo sapiens Q8WTV1 32814053
Intra
VBP1 P61758 MISP Homo sapiens Q8IVT2 32296183
Intra
VBP1 P61758 ZNF488 Homo sapiens Q96MN9-2 32814053
Intra
VBP1 P61758 ZNF488 Homo sapiens Q96MN9-2 32814053
Intra
VBP1 P61758 ZNF488 Homo sapiens Q96MN9-2 32814053
Intra
VBP1 P61758 UBL7 Homo sapiens Q96S82 25416956
Intra
VBP1 P61758 UBL7 Homo sapiens Q96S82 32296183
Intra
VBP1 P61758 UBL7 Homo sapiens Q96S82 25416956
Intra
VBP1 P61758 UBL7 Homo sapiens Q96S82 32296183
Intra
VBP1 P61758 UBL7 Homo sapiens Q96S82 33961781
Intra
VBP1 P61758 UBL7 Homo sapiens Q96S82 32296183
Intra
VBP1 P61758 UBL7 Homo sapiens Q96S82 28514442
Intra
VBP1 P61758 PFDN4 Homo sapiens Q9NQP4 32296183
Intra
VBP1 P61758 PFDN4 Homo sapiens Q9NQP4 32296183
Intra
VBP1 P61758 PFDN4 Homo sapiens Q9NQP4 25416956
Intra
VBP1 P61758 PFDN4 Homo sapiens Q9NQP4 32296183
Intra
VBP1 P61758 PFDN5 Homo sapiens Q99471 32296183
Intra
VBP1 P61758 PFDN5 Homo sapiens Q99471 33961781
Intra
VBP1 P61758 PFDN5 Homo sapiens Q99471 28514442
Intra
VBP1 P61758 PFDN5 Homo sapiens Q99471 32296183
Intra
VBP1 P61758 PFDN5 Homo sapiens Q99471 32296183
Intra
VBP1 P61758 PFDN2 Homo sapiens Q9UHV9 32814053
Intra
VBP1 P61758 PFDN2 Homo sapiens Q9UHV9 32814053
Intra
VBP1 P61758 PFDN2 Homo sapiens Q9UHV9 32296183
Intra
VBP1 P61758 PFDN2 Homo sapiens Q9UHV9 32814053
Intra
VBP1 P61758 ZNF576 Homo sapiens Q9H609 32296183
Intra
VBP1 P61758 GABPB1 Homo sapiens Q06547-2 32814053
Intra
VBP1 P61758 GABPB1 Homo sapiens Q06547-2 32814053
Intra
VBP1 P61758 GABPB1 Homo sapiens Q06547-2 32814053
Intra
VBP1 P61758 GLIS2 Homo sapiens Q9BZE0 32296183
Intra
VBP1 P61758 TSC22D4 Homo sapiens Q9Y3Q8 32296183
Intra
VBP1 P61758 TSC22D4 Homo sapiens Q9Y3Q8 32296183
Intra
VBP1 P61758 TSC22D4 Homo sapiens Q9Y3Q8 32296183
Intra
VBP1 P61758 DDIT4L Homo sapiens Q96D03 32296183
Intra
VBP1 P61758 EFHC1 Homo sapiens Q5JVL4 32296183
Intra
VBP1 P61758 ENKD1 Homo sapiens Q9H0I2 32296183
Intra
VBP1 P61758 MYOZ1 Homo sapiens Q9NP98 32296183
Intra
VBP1 P61758 ZNF581 Homo sapiens Q9P0T4 32814053
Intra
VBP1 P61758 ZNF581 Homo sapiens Q9P0T4 32814053
Intra
VBP1 P61758 ZNF581 Homo sapiens Q9P0T4 32814053
Intra
VBP1 P61758 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
VBP1 P61758 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
VBP1 P61758 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
VBP1 P61758 ZNF232 Homo sapiens Q9UNY5 32814053
Intra
VBP1 P61758 ZNF232 Homo sapiens Q9UNY5 32814053
Intra
VBP1 P61758 ZNF232 Homo sapiens Q9UNY5 32814053
Intra
VBP1 P61758 AIRIM Homo sapiens Q9NX04 32296183
Intra
VBP1 P61758 BECN1 Homo sapiens Q14457 32814053
Intra
VBP1 P61758 BECN1 Homo sapiens Q14457 32814053
Intra
VBP1 P61758 BECN1 Homo sapiens Q14457 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
X-Linked Intellectual Disability-Cardiomegaly-Congestive Heart Failure Syndrome
  • Mental Retardation, X-Linked, Syndromic 32

  • Mrxs32

Non-Syndromic X-Linked Intellectual Disability 72
  • Mrx72

Hypomelanosis Of Ito
  • Incontinentia Pigmenti Achromians

  • Nevus Of Ito

  • Ipa

  • Ito Hypomelanosis

  • Ito

  • Pigmentation Disorders

  • HMI

  • Incontinentia Pigmenti, Type I, Formerly

  • Ip1, Formerly

  • Bloch-Siemans Syndrome

  • Incontinentia Pigmenti Achromians Syndrome

  • Ito'S Nevus

  • Incontinentia Pigmenti Type 1

  • Nevi Of Ito

  • Nevus Fuscocaeruleus Acromiodeltoideus

  • Bloch Sulzberger Syndrome

  • Skin Pigmentation Disorder

Schimmelpenning-Feuerstein-Mims Syndrome
  • Nevus Sebaceus Of Jadassohn

  • Organoid Nevus Phakomatosis

  • Linear Nevus Sebaceous Syndrome

  • Sfm Syndrome

  • Jadassohn Nevus Phakomatosis

  • Jnp

  • Schimmelpenning Syndrome

  • Solomon Syndrome

  • SFM

  • Linear Sebaceous Nevus Syndrome

  • Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic

  • Nevus Sebaceus Syndrome

  • Organoid Nevus Syndrome

  • Schimmelpenning Feuerstein Mims Syndrome

  • Sebaceous Nevus Syndrome, Linear

  • Epidermal Nevus Syndrome, Formerly

  • Sebaceous Nevus Syndrome Linear

  • Linear Nevus Sebaceus Syndrome

  • Epidermal Nevus Syndrome

  • Ss

  • Nevus Sebaceous

Non-Syndromic X-Linked Intellectual Disability
  • X-Linked Non-Syndromic Intellectual Disability

  • Non-Specific X-Linked Mental Retardation

  • X-Linked Non-Specific Intellectual Disability

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

Orthologs Information

Species Symbol Source ID
Bos taurus VBP1 VGNC VGNC:36777
Mus musculus VBP1 MGD MGI:1333804
Rattus norvegicus VBP1 RGD RGD:1590535
Canis familiaris VBP1 VGNC VGNC:48239
Felis catus VBP1 VGNC VGNC:66929
Others VBP1 NCBI