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A Database of Extreme Multifunctional and Moonlighting Proteins
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Protein: Q9Y6X0
UniprotKB AC
UniprotKB ID
Gene name
Full name
Species
Curated set
Q9Y6X0 (Uniprot)
SETBP_HUMAN
SETBP1
SET-binding protein
human
No
Protein Function
No associated function.
MoonDB Dissimilar Functions
GO ID 1
Function 1
Module ID 1
GO ID 2
Function 2
Module ID 2
Association Probability
(PrOnto)
Interaction Probability
(PrOnto)
GO:0036211
protein modification process
201
GO:0006396
RNA processing
681
5.60e-03
3.14e-16
MoonDB Network Modules
Biological Processes
Module ID
(MoonGO)
GO ID (BP)
GO Name
191
GO:0006355
regulation of transcription, DNA-templated
201
GO:0006464
cellular protein modification process
201
GO:0031325
positive regulation of cellular metabolic process
201
GO:0010604
positive regulation of macromolecule metabolic process
201
GO:0051173
positive regulation of nitrogen compound metabolic process
201
GO:0010646
regulation of cell communication
201
GO:0023051
regulation of signaling
201
GO:0006355
regulation of transcription, DNA-templated
201
GO:0007165
signal transduction
463
GO:0090304
nucleic acid metabolic process
463
GO:0060255
regulation of macromolecule metabolic process
654
GO:0010467
gene expression
654
GO:0019538
protein metabolic process
654
GO:0060255
regulation of macromolecule metabolic process
681
GO:0008380
RNA splicing
681
GO:0006397
mRNA processing
681
GO:0051252
regulation of RNA metabolic process
681
GO:0010468
regulation of gene expression
753
GO:0044267
cellular protein metabolic process
753
GO:0034654
nucleobase-containing compound biosynthetic process
753
GO:0031325
positive regulation of cellular metabolic process
753
GO:0010604
positive regulation of macromolecule metabolic process
753
GO:0051173
positive regulation of nitrogen compound metabolic process
753
GO:0031326
regulation of cellular biosynthetic process
753
GO:0019219
regulation of nucleobase-containing compound metabolic process
753
GO:0009966
regulation of signal transduction
Cellular Components
Module ID
(MoonGO)
GO ID (CC)
GO Name
191
GO:0031981
nuclear lumen
201
GO:0005829
cytosol
201
GO:0005654
nucleoplasm
463
GO:0005654
nucleoplasm
654
GO:0005654
nucleoplasm
681
GO:0005654
nucleoplasm
753
GO:0005634
nucleus
Protein GO Annotations
Biological Processes
No results found.
Cellular Components
GO ID (CC)
GO Name
Evidence Code
(GO EC)
GO:0005634
nucleus
IDA
GO:0005829
cytosol
IDA
GO:0016604
nuclear body
IDA
Dissimilar Cellular Components (PrOnto)
No pairs of PrOnto dissimilar CC GO terms found.
All Protein Interactions
Interactor
Also a MoonDB EMF protein
G2XKQ0_HUMAN
No
A0FGX0_HUMAN
No
KAT6B_HUMAN
Yes:
Q8WYB5 (MoonDB)
LCHN_HUMAN
No
PKHF2_HUMAN
No
Q7KZS0_HUMAN
No
Q9P1C9_HUMAN
No
SET_HUMAN
No
SPNXA_HUMAN
No
SPNXC_HUMAN
No
SPNXD_HUMAN
No
UBC9_HUMAN
Yes:
P63279 (MoonDB)
XAGE1_HUMAN
No
YAF2_HUMAN
No
Publications Associated
PMID
Article Title
9455477
Prediction of the coding sequences of unidentified human genes. VIII. 78 new cDNA clones from brain which code for large proteins in vitro.
11231286
Identification and characterization of SEB, a novel protein that binds to the acute undifferentiated leukemia-associated protein SET.
12168954
Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones.
15489334
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
16177791
DNA sequence and analysis of human chromosome 18.
16959974
The consensus coding sequences of human breast and colorectal cancers.
19690332
Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.
20436468
De novo mutations of SETBP1 cause Schinzel-Giedion syndrome.
23222956
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia.
23628959
SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations.
23648668
SETBP1 mutation analysis in 944 patients with MDS and AML. Hannover, Germany.
23832011
Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia.
23832012
Somatic SETBP1 mutations in myeloid malignancies.
23889083
Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.
25217958
Refining analyses of copy number variation identifies specific genes associated with developmental delay.
OMIM Diseases Associated
OMIM ID
Disease Name
269150
Schinzel-Giedion midface retraction syndrome
601626
Leukemia, acute myelogenous
607785
Leukemia, juvenile myelomonocytic
608232
Leukemia, chronic myeloid, atypical
614286
Myelodysplastic syndrome
Protein Domains Associated
Domain Name
Domain ID
Source
AT_hook_DNA-bd_motif
IPR017956
InterPro
AT_hook
SM00384
SMART
T00063
T00063
PIR