Protein Vhl

URN urn:agi-llid:5952
Total Entities 0
Connectivity 252
Name Vhl
Description von Hippel-Lindau tumor suppressor
Notes Von Hippel-Lindau syndrome (VHL) is a dominantly inherited familial cancer syndrome predisposing to a variety of malignant and benign tumors. A germline mutation of this gene is the basis of familial inheritance of VHL syndrome. The protein encoded by this gene is a component of the protein complex that includes elongin B, elongin C, and cullin-2, and possesses ubiquitin ligase E3 activity. This 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. RNA polymerase II subunit POLR2G/RPB7 is also reported to be a target of this protein. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq]

Ariadne Ontology Ubiquitin-dependent protein degradation
Tumor suppressors
Secreted proteins
Biofluids assayable substances

GO Molecular Function protein complex binding
transcription factor binding
enzyme binding
ubiquitin-protein ligase activity

GO Cellular Component membrane
nucleoplasm
transcription factor complex
VCB complex
cytoplasm
mitochondrion
cytosol
endoplasmic reticulum
nucleus

GO Biological Process positive regulation of transcription, DNA-dependent
negative regulation of transcription from RNA polymerase II promoter
negative regulation of transcription from RNA polymerase II promoter in response to hypoxia
regulation of transcription, DNA-dependent
regulation of transcription from RNA polymerase II promoter in response to hypoxia
regulation of catecholamine metabolic process
negative regulation of cell proliferation
negative regulation of apoptotic process
positive regulation of cell differentiation
cell morphogenesis
neuron differentiation
protein ubiquitination
blood vessel endothelial cell migration
cellular response to stress
cellular response to hypoxia
extracellular matrix organization
response to stress
response to ethanol
response to hypoxia
protein stabilization
angiogenesis
proteolysis
protein catabolic process
proteasomal protein catabolic process
protein heterooligomerization

Pathway hypoxia inducible factor pathway
altered hypoxia inducible factor pathway
renal cell cancer pathway
renal cell cancer pathway
renal cell cancer pathway

Group Ubiquitin-dependent protein degradation
Tumor suppressors
positive regulation of transcription, DNA-dependent
negative regulation of transcription from RNA polymerase II promoter
negative regulation of transcription from RNA polymerase II promoter in response to hypoxia
regulation of transcription, DNA-dependent
regulation of transcription from RNA polymerase II promoter in response to hypoxia
regulation of catecholamine metabolic process
negative regulation of cell proliferation
negative regulation of apoptotic process
positive regulation of cell differentiation
cell morphogenesis
neuron differentiation
protein ubiquitination
blood vessel endothelial cell migration
cellular response to stress
cellular response to hypoxia
extracellular matrix organization
response to stress
response to ethanol
response to hypoxia
protein stabilization
angiogenesis
proteolysis
protein catabolic process
proteasomal protein catabolic process
protein heterooligomerization
protein complex binding
transcription factor binding
enzyme binding
ubiquitin-protein ligase activity
membrane
nucleoplasm
transcription factor complex
VCB complex
cytoplasm
mitochondrion
cytosol
endoplasmic reticulum
nucleus
Secreted proteins
Biofluids assayable substances

MedScan ID 5952

Hugo ID 12687

Human chromosome position 3p25.3
3p26-p25

GenBank ID NC_000003
NM_000551
NP_000542
NM_198156
NP_937799
NG_008212
NC_018914
AC_000135
AC034193
AF010238
AAB64200
CH471055
EAW64064
EAW64065
EAW64066
EAW64067
EAW64068
HI574030
CBX47504
HI574032
CBX47505
U54612
AAA98614
X96489
CAA65343
AA361862
AF088066
AK304002
BAG64919
AK309560
AK315799
BAG38142
AW022843
BC027957
AAH27957
BC058831
AAH58831
BG284971
BG288777
BG914051
BM564781
BX100230
D58014
L15409
P40337
NC_000072
NM_009507
NP_033533
AC_000028
AC153987
AF513984
AAM53645
CH466523
EDK99490
EDK99491
AK159238
BAE34921
AK161408
BAE36378
AK171264
BAE42352
AK171604
BAE42557
BC052417
AAH52417
S76748
AAB33363
U12570
AAA20662
P40338
NC_005103
NM_052801
NP_434688
AC_000072
CH473957
EDL91551
EDL91552
S80345
AAB35675
U14746
AAA86874
Q64259
NT_022517
NW_001838876
NW_921651
AC_000046
NT_039353
NW_001030811
Q3TTE7
NW_001084830
NW_047696

LocusLink ID 5952
7428
22346
24874

Alias RCA1
VHL1
pVHL
HRCA1
von Hippel-Lindau disease tumor suppressor
protein G7
elongin binding protein
Vhlh
von Hippel-Lindau syndrome homolog
von Hippel-Lindau syndrome protein homolog
Von Hippel-Lindau disease tumour suppressor
von Hippel-Lindau syndrome gene
von Hippel-Lindau syndrome protein
von Hippel-Lindau tumour suppressor
RCA I
von Hippel-Lindau tumor suppressor
VHL gene
renal carcinoma, familial, associated 1
OTTMUSP00000028703
HRCA I
G7 PROTEIN
VHL protein
elongin-binding protein

Organism Homo sapiens
Mus musculus
Rattus norvegicus

OMIM ID 608537
263400
171300
144700
193300

Unigene ID Hs.517792
Mm.29407
Rn.11059

KEGG ID hsa:7428
mmu:22346
rno:24874

Swiss-Prot Accession P40337
P40338
Q3TTE7
Q64259
Q64197
Q80WY8
B2RE45
Q13599
Q6PDA9

GO ID 0019899
0008134
0004842
0000902
0071456
0033554
0043066
0008285
0000122
0061428
0045597
0045893
0050821
0016567
0006508
0061418
0006355
0006950
0005829
0005783
0016020
0005739
0005654
0005634
0032403
0001525
0043534
0030198
0030182
0010498
0030163
0051291
0042069
0001666
0030891
0005737
0045471
0005667
0006916
0045941
0045449
0019941

PIR ID T10752
I38926

Swiss-Prot ID VHL_MOUSE
VHL_RAT
VHL_HUMAN
Q3TTE7_MOUSE

Cell Localization Cytoplasm
Membrane
Nucleus

IPI ID IPI00109233
IPI00210924
IPI00027969
IPI00336024
IPI00939404
IPI00221186
IPI00792496

Mouse chromosome position 6 49.45 cM

Rat chromosome position 4q41.3-q42.1

Homologene ID 465

MGI ID 103223

RGD ID 3960

Primary Cell Localization Cytoplasm