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ID1 and SUV39H1
Number of citations of the paper that reports this interaction (PubMedID
23455924
)
46
Data Source:
BioGRID
(two hybrid)
ID1
SUV39H1
Description
inhibitor of DNA binding 1, HLH protein
SUV39H1 histone lysine methyltransferase
Image
No pdb structure
GO Annotations
Cellular Component
Nucleus
Nucleoplasm
Golgi Apparatus
Centrosome
Chromosome, Centromeric Region
Heterochromatin
Condensed Nuclear Chromosome
Nucleus
Nuclear Lamina
Nucleoplasm
Chromatin Silencing Complex
RDNA Heterochromatin
Molecular Function
Protein Binding
Protein C-terminus Binding
Identical Protein Binding
Protein Dimerization Activity
Protein N-terminus Binding
Proteasome Binding
Transcription Regulator Activity
Transcription Regulator Inhibitor Activity
Transcription Cis-regulatory Region Binding
Chromatin Binding
Protein Binding
Zinc Ion Binding
S-adenosylmethionine-dependent Methyltransferase Activity
Histone-lysine N-methyltransferase Activity
Histone Methyltransferase Activity
Histone Methyltransferase Activity (H3-K9 Specific)
Protein N-terminus Binding
Biological Process
Negative Regulation Of Transcription By RNA Polymerase II
Angiogenesis
Transforming Growth Factor Beta Receptor Signaling Pathway
Brain Development
Negative Regulation Of Transcription By Transcription Factor Localization
Positive Regulation Of Gene Expression
Cell Differentiation
Neuron Differentiation
Negative Regulation Of Protein Binding
Positive Regulation Of Actin Filament Bundle Assembly
Circadian Regulation Of Gene Expression
Cell-abiotic Substrate Adhesion
Negative Regulation Of Apoptotic Process
Negative Regulation Of DNA Binding
Negative Regulation Of DNA-binding Transcription Factor Activity
Blood Vessel Endothelial Cell Migration
Negative Regulation Of Endothelial Cell Differentiation
Negative Regulation Of Transcription, DNA-templated
Blood Vessel Morphogenesis
Positive Regulation Of Epithelial Cell Proliferation
Negative Regulation Of Dendrite Morphogenesis
Cellular Response To Epidermal Growth Factor Stimulus
Negative Regulation Of Cold-induced Thermogenesis
Regulation Of Vasculature Development
Cellular Response To Peptide
Cellular Response To Dopamine
Cellular Response To Nerve Growth Factor Stimulus
Negative Regulation Of Transcription By RNA Polymerase II
RDNA Heterochromatin Assembly
Chromatin Organization
RRNA Processing
Cellular Response To DNA Damage Stimulus
Cell Cycle
Cell Differentiation
Histone Lysine Methylation
Histone H3-K9 Dimethylation
Histone H3-K9 Trimethylation
Negative Regulation Of Circadian Rhythm
Negative Regulation Of Transcription, DNA-templated
Rhythmic Process
Cellular Response To Hypoxia
Pathways
Oncogene Induced Senescence
NGF-stimulated transcription
PKMTs methylate histone lysines
SIRT1 negatively regulates rRNA expression
Drugs
Diseases
GWAS
Diastolic blood pressure (
27841878
)
Systolic blood pressure (
27841878
)
Interacting Genes
27 interacting genes:
AAR2
APPL1
ASCL3
ASXL1
CASK
COPB1
DNMT3L
ELK1
ELK4
GATA4
HES1
IFI16
IKBKG
MSGN1
MYF5
MYF6
MYOD1
MYOG
POFUT1
PSMD4
RUNX1T1
SUV39H1
TCF12
TCF3
TCF4
TRIM55
TRIM63
137 interacting genes:
ATE1
ATF3
ATP6V1B1
BAHD1
BCL11B
C4orf17
C8orf74
CBX1
CBX4
CBX5
CDC23
CDCA4
CDCA7L
CEP70
CFAP100
CLK3
CRBN
CREBBP
CRELD2
DBF4B
DCAF8
DDB1
DNMT1
DNMT3A
DNMT3B
DVL3
ELOF1
EP300
ESR1
EZH2
FGD5
FOXR2
FRMD6
FUS
FYN
GOLGA6L9
GPATCH2L
GTF2H2C_2
GTPBP2
H3-3A
H3-4
H3-5
H3C1
H3C15
HDAC1
HDAC2
HDAC3
HDAC5
HOOK2
HOXA1
HOXC4
ID1
ID2
IGFBP4
IL16
ING4
INTS2
KDM1A
KLF15
KLHDC4
KLHL20
KRTAP10-7
KRTAP10-8
LDHAL6B
LENG8
LHX8
LINC02875
LNX1
LOXL4
LZTS2
MALT1
MBD1
MBD4
MCRS1
MSANTD3
MTF2
MTO1
MYOD1
NR1H2
NR1H3
ODAD3
OPA3
PADI6
PHF19
PML
PNKP
PPP1R16A
PRIM2
PRMT6
PSMC1
RASSF1
RASSF2
RB1
RBBP4
RBBP7
RBL1
RBL2
RIN3
RRP8
RSPO2
RUNX1
SBF1
SLFN12
SMAD1
SMAD5
SPATA24
SPRED1
SPSB1
SRGAP3
STX11
STX19
TEKT4
TEX35
THRA
TMEM11
TNFAIP1
TNS2
TRIM41
U2AF1
WDFY3
WIZ
ZBTB2
ZBTB24
ZCCHC17
ZKSCAN5
ZNF165
ZNF417
ZNF436
ZNF438
ZNF451
ZNF557
ZNF581
ZNF649
ZNF670
ZNF829
ZRANB1
ZSCAN9
Entrez ID
3397
6839
HPRD ID
08980
02221
Ensembl ID
ENSG00000125968
ENSG00000101945
Uniprot IDs
P41134
O43463
PDB IDs
3MTS
Enriched GO Terms of Interacting Partners
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