1. Gene
  2. VHL - von Hippel-Lindau tumor suppressor Gene

VHL - von Hippel-Lindau tumor suppressor Gene

Homo sapiens

Also known as RCA1; VHL1; pVHL; HRCA1

Gene ID: 7428 | Gene type: protein coding

About VHL

Cytogenetic location: 3p25.3 Genomic coordinates (GRCh38): 3:10,141,778-10,153,667 (from NCBI)

This gene has 6 transcripts (splice variants), 168 orthologues, 1 paralogue and is associated with 102 phenotypes. Ubiquitous expression in lymph node (RPKM 12.2), spleen (RPKM 10.0) and 25 other tissues.

Summary

This gene encodes a component of a ubiquitination complex. The encoded protein is involved in the ubiquitination and degradation of hypoxia-inducible-factor (HIF), which is a transcription factor that plays a central role in the regulation of gene expression by oxygen. In addition to oxygen-related gene expression, this protein plays a role in many Other cellular processes including cilia formation, cytokine signaling, regulation of senescence, and formation of the extracellular matrix. Variants of this gene are associated with von Hippel-Lindau syndrome, pheochromocytoma, erythrocytosis, renal cell carcinoma, and cerebellar hemangioblastoma. [provided by RefSeq, Jun 2022]

VHL Products(3)

mRNA Protein Name
NM_000551.4 NP_000542.1 von Hippel-Lindau disease tumor suppressor isoform 1
NM_001354723.2 NP_001341652.1 von Hippel-Lindau disease tumor suppressor isoform 3
NM_198156.3 NP_937799.1 von Hippel-Lindau disease tumor suppressor isoform 2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
11641274 GOA
enables enzyme binding IPI
IPI: Inferred from physical interaction
11641274 GOA
enables molecular adaptor activity EXP
EXP: Inferred from Experiment
10205047 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
7660122 GOA
enables transcription elongation factor activity IDA
IDA: Inferred from direct assay
7660122 GOA
enables ubiquitin-like ligase-substrate adaptor activity IDA
IDA: Inferred from direct assay
24899725 GOA
Biological Process GO Annotation Evidence Reference Source
involved in amyloid fibril formation EXP
EXP: Inferred from Experiment
34431623 GOA
involved in amyloid fibril formation IDA
IDA: Inferred from direct assay
34431623 GOA
involved in negative regulation of TORC1 signaling IDA
IDA: Inferred from direct assay
34290272 GOA
involved in negative regulation of autophagy IDA
IDA: Inferred from direct assay
30902965 GOA
involved in negative regulation of cell population proliferation IDA
IDA: Inferred from direct assay
23338840 GOA
involved in negative regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
23338840 GOA
involved in negative regulation of gene expression IMP
IMP: Inferred from mutant phenotype
23338840 GOA
involved in negative regulation of receptor signaling pathway via JAK-STAT IMP
IMP: Inferred from mutant phenotype
23338840 GOA
involved in negative regulation of signal transduction EXP
EXP: Inferred from Experiment
23338840 GOA
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
11641274 GOA
involved in negative regulation of transcription elongation by RNA polymerase II IDA
IDA: Inferred from direct assay
7660122 GOA
involved in positive regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
17973242 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IDA
IDA: Inferred from direct assay
34290272 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
24899725 GOA
involved in protein ubiquitination IMP
IMP: Inferred from mutant phenotype
12169691 GOA
involved in regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
15824735 GOA
involved in regulation of cellular response to hypoxia EXP
EXP: Inferred from Experiment
10205047 GOA
involved in regulation of gene expression EXP
EXP: Inferred from Experiment
15824735 GOA
involved in regulation of gene expression IDA
IDA: Inferred from direct assay
17973242 GOA
involved in regulation of gene expression IEP
IEP: Inferred from expression pattern
15824735 GOA
Cellular Component GO Annotation Evidence Reference Source
is active in endoplasmic reticulum IDA
IDA: Inferred from direct assay
34290272 GOA
is active in intracellular non-membrane-bounded organelle EXP
EXP: Inferred from Experiment
14963040 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

VHL Protein Structure

VHL

VHL: VHL beta domain (58 - 213)

  • 0
  • 100
  • 200
  • 213 a.a.
Protein Preferred Names Protein Names

von Hippel-Lindau disease tumor suppressor

elongin binding protein

VHL Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
VHL P40337 FN1 Homo sapiens P02751
Anti Tag CoIP
18323857
Intra
VHL P40337 RNF139 Homo sapiens Q8WU17
Anti Bait CoIP
12032852
Cross
VHL P40337 P0C6X7-PRO_0000037322 Human SARS coronavirus P0C6X7-PRO_0000037322
Anti Tag CoIP
25732088
Cross
VHL P40337 P0C6X7-PRO_0000037322 Human SARS coronavirus P0C6X7-PRO_0000037322
Confocal
25732088
Cross
VHL P40337 P0C6X7-PRO_0000037322 Human SARS coronavirus P0C6X7-PRO_0000037322
Pull Down
25732088
Intra
VHL P40337 PRKCZ Homo sapiens Q05513
Anti Tag CoIP
17350623
Intra
VHL P40337 PRKCZ Homo sapiens Q05513
Imaging
17350623
Intra
VHL P40337 RACK1 Homo sapiens P63244
Anti Tag CoIP
20871634
Intra
VHL P40337 RACK1 Homo sapiens P63244
Y2H
20871634
Intra
VHL P40337 RACK1 Homo sapiens P63244
Pull Down
20871634
Cross
VHL P40337 Hif1a Mus musculus Q61221
Anti Bait CoIP
11292862
Cross
VHL P40337 Hif1a Mus musculus Q61221
Far-WB
11292862
Intra
VHL P40337 HIF1A Homo sapiens Q16665
Anti Bait CoIP
11292862
Intra
VHL P40337 HIF1A Homo sapiens Q16665
Anti Tag CoIP
21602890
Intra
VHL P40337 HIF1A Homo sapiens Q16665
Pull Down
11292862
Intra
VHL P40337 HIF1A Homo sapiens Q16665
Anti Tag CoIP
34818544
Intra
VHL P40337 CUL2 Homo sapiens Q13617
Anti Bait CoIP
15601820
Intra
VHL P40337 CUL2 Homo sapiens Q13617
Anti Tag CoIP
33961781
Intra
VHL P40337 CUL2 Homo sapiens Q13617
Anti Tag CoIP
15601820
Intra
VHL P40337 CUL2 Homo sapiens Q13617
Pull Down
25661653
Intra
VHL P40337 CUL2 Homo sapiens Q13617
Anti Tag CoIP
18323857
Intra
VHL P40337 CUL2 Homo sapiens Q13617
Anti Bait CoIP
17353931
Intra
VHL P40337 MDFI Homo sapiens Q99750
Y2H Prey Pooling
25416956
Intra
VHL P40337 TGM2 Homo sapiens P21980
Anti Bait CoIP
21625219
Intra
VHL P40337 TGM2 Homo sapiens P21980
Enzymatic Study
21625219
Intra
VHL P40337 TGM2 Homo sapiens P21980
Anti Tag CoIP
21625219
Intra
VHL P40337 PRMT1 Homo sapiens Q99873
Anti Tag CoIP
23455924
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant VHL Proteins

Cat. No. Product Name Accession Purity
HY-P76124 VHL Protein, Human (His) P40337 (M1-D213) ≥95%

Related Diseases

Diseases Alias
Von Hippel-Lindau Syndrome

Von Hippel-Lindau Disease

Vhl

Vhl Syndrome

VHLS

Von Hippel-Lindau Syndrome, Modifier Of

Hippel Lindau Syndrome

Angiomatosis Retinae

Cerebelloretinal Angiomatosis, Familial

Hippel-Lindau Disease

Familial Cerebelloretinal Angiomatosis

Lindau Disease

VHLD

Erythrocytosis, Familial, 2

Chuvash Polycythemia

ECYT2

Familial Erythrocytosis 2

Autosomal Recessive Benign Erythrocytosis

Polycythemia, Vhl-Dependent

Chuvash Erythromatosis

Chuvash Type Polycythemia

Chuvash Erythrocytosis

Von Hippel-Lindau-Dependent Polycythemia

Polycythemia Chuvash Type

Vhl-Dependent Polycythemia

Erythrocytosis, Familial, Type 2

Renal Cell Carcinoma, Nonpapillary

Renal Cell Carcinoma

RCC

Nonpapillary Renal Cell Carcinoma

Clear Cell Renal Cell Carcinoma

Hypernephroma

Adenocarcinoma Of Kidney

Renal Carcinoma, Chromophobe, Somatic

Clear Cell Carcinoma Of Kidney

Clear-Cell Metastatic Renal Cell Carcinoma

Clear Cell Renal Carcinoma

Renal Cell Carcinoma, Somatic

Conventional Renal Cell Carcinoma

Conventional Renal Cell Carcinoma

Renal Clear Cell Carcinoma

Ccrcc

Hereditary Clear Cell Renal Cell Carcinoma

Carcinoma, Renal Cell

Renal Cell Carcinoma, Clear Cell, Somatic

Renal Cell Carcinoma, Clear Cell

Clear Cell Kidney Carcinoma

Clear Cell Rcc

Cystic-Multilocular Variant

Clear Cell Renal Cell Adenocarcinoma

Hereditary Clear Cell Renal Cell Adenocarcinoma

Common Renal Cell Carcinoma

Crcc

Renal Cell Carcinoma Non-Papillary

Carcinoma Renal Cell

Renal Cell Cancer

Carcinoma, Renal Cell, Nonpapillary

Pheochromocytoma

Pheochromocytoma, Susceptibility To

Phaeochromocytoma

Adrenal Gland Chromaffin Paraganglioma

Adrenal Gland Chromaffinoma

Adrenal Gland Paraganglioma

Adrenal Gland Pheochromocytoma

Chromaffin Paraganglioma Of The Adrenal Gland

Intraadrenal Paraganglioma

PCC

Chromaffin Cell Tumor

Medullary Chromaffinoma

Medullary Paraganglioma

Pheochromoblastoma

Pheochromocytomas

Chromaffin Cell Neoplasm

Pheochromocytoma, Malignant

Retinal Hemangioblastoma

Capillary Hemangioma Of Retina

Acute Biphenotypic Leukemia

Mixed Phenotype Acute Leukemia

Acute Leukemia Of Ambiguous Lineage

Acute Undifferentiated Leukemia

Acute Leukemia Of Indeterminate Lineage

Hybrid Acute Leukemia

Mixed Lineage Acute Leukemia

All With Myeloid Markers

Aml With Lymphoid Markers

Acute Leukemia Of Undetermined Lineage

Bal

Biphenotypic Acute Leukemia

Undifferentiated Acute Leukemia

Mpal

Acute Myeloid Leukemia, Minimal Differentiation, Fab M0

Leukemia, Biphenotypic, Acute

Myasthenic Syndrome, Congenital, 6, Presynaptic

Familial Infantile Myasthenia

CMS6

Cmsea

Congenital Myasthenic Syndrome 6

Familial Infantile Myasthenia Gravis 2

Fimg2

Myasthenic Syndrome, Congenital, Associated With Episodic Apnea

Myasthenic Syndrome, Presynaptic, Congenital, Associated With Episodic Apnea

Congenital Myasthenic Syndrome Type Ia2, Formerly

Cms1a2, Formerly

Cms Ia2, Formerly

Myasthenia, Familial Infantile, Formerly

Fim, Formerly

Myasthenia Gravis, Familial Infantile, 2, Formerly

Fimg2, Formerly

Cms Ia2

Cms1a2

Congenital Myasthenic Syndrome 6, Presynaptic

Congenital Myasthenic Syndrome Type Ia2

Congenital Presynaptic Myasthenic Syndrome Associated With Episodic Apnea

Fim

Cms1a

Cms-Ea

Cms Ia

Congenital Myasthenic Syndrome Pre-Synaptic Associated With Episodic Apnea

Congenital Myasthenic Syndrome Type 1a

Congenital Myasthenic Syndrome Type Ia

Myasthenic Syndrome, Congenital, Type 6, Presynaptic

Renal Cell Carcinoma, Papillary, 1

Papillary Renal Cell Carcinoma

Hereditary Papillary Renal Cell Carcinoma

Papillary Renal Cell Carcinoma, Sporadic

Papillary Renal Cell Adenocarcinoma

RCCP

RCCP1

Renal Cell Carcinoma, Papillary

Renal Cell Carcinoma, Papillary, 1, Familial And Somatic

Chromophil Carcinoma Of Kidney

Papillary Kidney Carcinoma

Sporadic Papillary Renal Cell Carcinoma

Chromophil Renal Cell Carcinoma

Papillary Renal Carcinoma, Malignant -

Papillary Renal Cell Carcinoma, Bilateral -

Papillary Renal Cell Carcinoma, Familial -

Papillary Renal Cell Carcinoma, Multiple -

Papillary Renal Cell Carcinoma, Sporadic -

Renal Adenocarcinoma

Chromophil Rcc

Hprcc

Renal Cell Carcinoma Papillary

Chromophilic Renal Cell Carcinoma

Prcc

Carcinoma, Renal Cell, Papillary, Type 1

Type 1 Papillary Renal Cell Carcinoma

Renal Cell Carcinoma

Hereditary Papillary Renal Carcinoma

Hereditary Paraganglioma-Pheochromocytoma Syndromes

Hereditary Pheochromocytoma-Paraganglioma

Hereditary Paraganglioma-Pheochromocytoma

Familial Pheochromocytoma-Paraganglioma

Paragangliomas 2

Paragangliomas 3

Paragangliomas 4

Sdhx-Related Paraganglioma-Pheochromocytoma

Familial Paraganglioma Syndrome

Familial Paraganglioma-Pheochromocytoma Syndromes

Fpgl

Fpgl/Pheo

Paragangliomas 1

Paraganglioma

Bap1 Tumor Predisposition Syndrome

Bap1-Related Tumor Predisposition Syndrome

Common Syndrome

Bap1 Cancer Syndrome

Bap1-Tpds

Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, And Other Internal Neoplasms

Tumor Predisposition Syndrome

Tumor Susceptibility Linked To Germline Bap1 Mutations

Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, Other Internal Neoplasms

Tumor Predisposition

Inherited Cancer-Predisposing Syndrome

Hereditary Cancer-Predisposing Syndrome

Hemangioblastoma

Capillary Hemangioblastoma

Microcystic Adenoma

Adenoma Microcystic

Adenoma, Microcystic

Sporadic Pheochromocytoma/Secreting Paraganglioma
Cystadenoma

Cystoma

Craniopharyngioma

Polycythemia

Erythrocythemia

Polycythemia Vera

Polycythaemia Due To High Altitude

Paraganglioma

Chemodectoma

Glomus Body Tumor

Paragangliomas

Carotid Body Paraganglioma

Extra-Adrenal Paraganglioma

Primary Polycythemia

Familial Erythrocytosis

Familiar Polycythemia

Benign Familial Polycythemia

Congenital Erythrocytosis

Familial Polycythemia

Hereditary Erythrocytosis

Primary Familial Polycythemia

Erythrocytosis, Familial

Polycythemia Vera

Primary Familial Polycythaemia

Primary Inherited Polycythaemia

Multiple Endocrine Neoplasia

Men

Multiple Endocrine Adenomatosis

Multiple Endocrine Neoplasia Syndrome

Adenomatosis, Familial Endocrine

Endocrine Neoplasia, Multiple

Familial Endocrine Adenomatosis

Mea

Multiple Endocrine Neoplasms

Multiple Endocrine Neoplasia Type 1

Hemangioma Of Liver

Hepatic Hemangioma

Angioma Of Liver

Hepatic Angioma

Collecting Duct Carcinoma

Kidney Medullary Carcinoma

Renal Medullary Carcinoma

Bdc

Bellini Carcinoma

Bellini Duct Carcinoma

Cdc

Collecting Duct Carcinoma Of The Kidney

Renal Cell Adenocarcinoma

Carcinoma Of Renal Collecting Duct

Renal Carcinoma, Collecting Duct Type

Renal Cell Carcinoma

Bellini'S Duct Carcinoma

Renal Collecting Duct Carcinoma

Adenocarcinoma Of Kidney

Kidney Cancer

Renal Cancer

Renal Carcinoma

Kidney Neoplasm

Malignant Neoplasm Of Kidney Except Pelvis

Malignant Tumour Of Kidney

Kidney Neoplasms

Cancer, Kidney

Cancer, Renal

Malignant Neoplasm Of Kidney

Renal Cell Carcinoma

Hepatoblastoma
Tuberous Sclerosis

Tuberous Sclerosis Syndrome

Bourneville'S Disease

Epiloia

Cerebral Sclerosis

Tuberose Sclerosis

Tuberous Sclerosis 1

Bourneville Disease

Bourneville Phakomatosis

Pringle'S Disease

Multiple Endocrine Neoplasia, Type Iia

Multiple Endocrine Neoplasia Type 2a

Sipple Syndrome

Multiple Endocrine Neoplasia Type 2

MEN2A

Men2

Ptc Syndrome

Multiple Endocrine Neoplasia, Type 2

Multiple Endocrine Neoplasia Iia

Men 2a

Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma

Multiple Endocrine Neoplasia, Type 2a

Pheochromocytoma And Amyloid-Producing Medullary Thyroid Carcinoma

Multiple Endocrine Neoplasia Ii

Men2 Syndrome

Men-2a Syndrome

Multiple Neoplasia 2a

Multiple Neoplasia Type 2

Leiomyomatosis
Fumarate Hydratase Deficiency

Fumarase Deficiency

Fumaric Aciduria

Pancreatic Serous Cystadenoma
Cystic Kidney Disease

Renal Cyst

Simple Renal Cyst

Kidney Cysts

Kidney Diseases, Cystic

Renal Cysts

Kidney Cyst

Cystic Kidney

Congenital Cystic Kidney Disease

Cystic Kidney Diseases

Bosniak 1 Cyst

Chromophobe Renal Cell Carcinoma

Chromophobe Adenocarcinoma

Chromophobe Carcinoma Of Kidney

Kidney Chromophobe

Renal Cell Carcinoma, Chromophobe Cell

Crcc

Chrcc

Chromophobe Renal Cell Adenocarcinoma

Chromophobe Renal Carcinoma

Chromophobe Carcinoma

Neurofibromatosis

Neurofibromatoses

Acoustic Neurofibromatosis

Central Neurofibromatosis

Peripheral Neurofibromatosis

Recklinghausen'S Neurofibromatosis

Von Reklinghausen Disease

Neurofibromatosis Type 1

Oncocytoma

Oxyphilic Adenoma

Follicular Adenoma, Oxyphilic Cell

Adenoma, Oxyphilic

Hurthle Cell Tumor

Oncocytic Neoplasm

Neurofibromatosis, Type I

Von Recklinghausen Disease

Neurofibromatosis 1

Neurofibromatosis, Type 1

NF1

Neurofibromatosis, Peripheral Type

Neurofibromatosis Type I

Neurofibromatosis Type 1 Due To Nf1 Mutation Or Intragenic Deletion

Familial Spinal Neurofibromatosis

Fsnf

Peripheral Neurofibromatosis

Von Recklinghausen'S Neurofibromatosis

Von Recklinghausen Disease Due To Nf1 Mutation Or Intragenic Deletion

Neurofibromatosis Peripheral Type

Von Recklinghausen Syndrome

Neurofibromatosis Type 1

Von Recklinghausen Neuropathy

Nf1 - [Neurofibromatosis Type 1]

Recklinghausen Disease

Central Nervous System Hemangioma

Hemangioma Of Cns

Hemangioma Of The Central Nervous System

Cardiovascular Organ Benign Neoplasm
Thyroid Carcinoma, Familial Medullary

Medullary Thyroid Carcinoma

Familial Medullary Thyroid Carcinoma

MTC

Medullary Thyroid Cancer

Fmtc

Mtc1

Thyroid Cancer, Medullary

Thyroid Carcinoma, Medullary

Familial Mtc

Thyroid Carcinoma Medullary

Carcinoma, Thyroid, Medullary, Familial

Medullary Carcinoma Of Thyroid

Medullary Carcinoma With Amyloid Stroma, Unspecified Site

Medullary Carcinoma With Amyloid Stroma Of Thyroid

Hemangioma

Hemangiomas

Middle Ear Adenocarcinoma

Adenocarcinoma Of Middle Ear

Adenocarcinoma Of The Middle Ear

Multiple Endocrine Neoplasia, Type I

Multiple Endocrine Neoplasia Type 1

MEN1

Wermer Syndrome

Multiple Endocrine Neoplasia 1

Multiple Endocrine Neoplasia, Type 1

Men I

Endocrine Adenomatosis, Multiple

Mea I

Men Type I

Wermer'S Syndrome

Men1 Syndrome

Multiple Endocrine Adenomatosis

Endocrine Adenomatosis Multiple

Men 1

Familial Multiple Endocrine Neoplasia Type I

Neoplasia, Endocrine, Multiple, Type 1

Multiple Endocrine Neoplasia

Hereditary Renal Cell Carcinoma
Lung Cancer

Lung Carcinoma

Non-Small Cell Lung Carcinoma

Lung Cancer, Susceptibility To

Lung Cancer, Protection Against

Adenocarcinoma Of Lung, Somatic

Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer

Lung Neoplasm

Carcinoma Of Lung

Lung Non-Small Cell Carcinoma

Non-Small Cell Lung Cancer

Nsclc

Lung Neoplasms

Malignant Neoplasm Of Lung

Alveolar Cell Carcinoma

Nonsmall Cell Lung Cancer, Somatic

Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer, Susceptibility To

Lung Cancer, Somatic

Lung Cancer, Resistance To

Cancer Of Lung

Cancer Of Bronchus

Cancer Of The Lung

Lung Malignancies

Lung Malignant Tumors

Malignant Lung Tumor

Malignant Tumor Of Lung

Pulmonary Cancer

Pulmonary Carcinoma

Pulmonary Neoplasms

Respiratory Carcinoma

LNCR

Adenocarcinoma Of Lung

Neoplasm Of Lung

Cancer Lung

Carcinoma Non-Small Cell Lung

Carcinoma, Non-Small-Cell Lung

Lung Cancers

Lung Carcinomas

Cancer, Lung

Cancer, Lung, Non-Small Cell

Primary Malignant Neoplasm Of Lung

Bronchioloalveolar Adenocarcinoma

Polycystic Kidney Disease

Polycystic Kidney Diseases

Pkd

Polycystic Renal Disease

Kidney Disease, Polycystic

Polycystic Kidney, Autosomal Dominant

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 VHL VGNC VGNC:97325
Rattus norvegicus VHL RGD RGD:3960
Mus musculus VHL MGD MGI:103223
Others VHL NCBI