Von Hippel–Lindau tumor suppressor

VHL
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesVHL, HRCA1, RCA1, VHL1, pvon Hippel-Lindau tumor suppressor
External IDsOMIM: 608537; MGI: 103223; HomoloGene: 465; GeneCards: VHL; OMA:VHL - orthologs
Orthologs
SpeciesHumanMouse
Entrez

7428

22346

Ensembl

ENSG00000134086

ENSMUSG00000033933

UniProt

P40337

P40338

RefSeq (mRNA)

NM_000551
NM_198156
NM_001354723

NM_009507

RefSeq (protein)

NP_000542
NP_937799
NP_001341652
NP_000542.1

NP_033533

Location (UCSC)Chr 3: 10.14 – 10.15 MbChr 6: 113.6 – 113.61 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

The Von Hippel–Lindau tumor suppressor also known as pVHL is a protein that, in humans, is encoded by the VHL gene. Mutations of the VHL gene are associated with Von Hippel–Lindau disease, which is characterized by hemangioblastomas of the brain, spinal cord and retina. It is also associated with kidney and pancreatic lesions.