IQSEC1 CAVIN4 AGAP9 RASGRF1 TBC1D22A GPS2 NUCB2

IQSEC1 CAVIN4 AGAP9 RASGRF1 TBC1D22A GPS2 NUCB2

DHX36 ICE1 SF3B1

ICE1 SUPT6H SUPT16H

MYH10 RAB11FIP4 TUBGCP2

GOLGA5 NUCB2

DGCR6 DGCR6L

DGCR6 DGCR6L

IQSEC1 CEP131 MYH10 RASGRF1

IQSEC1 CEP131 MYH10 RASGRF1

IQSEC1 CEP131 MYH10 RASGRF1

CEP131 MYH10 RASGRF1

ZNF830 SCAPER

ZNF830 SCAPER

WDR87 EML6

BRSK1 NUAK1

RAB11FIP4 USP32 NUCB2

Human Antiviral Protein IFIX Suppresses Viral Gene Expression during Herpes Simplex Virus 1 (HSV-1) Infection and Is Counteracted by Virus-induced Proteasomal Degradation.

CUL3 LAMA4 DHX36 PHF3 SUPT6H UTP14A SUPT16H

Identification of motif-based interactions between SARS-CoV-2 protein domains and human peptide ligands pinpoint antiviral targets.

IQSEC1 SF3B1 GOLGA5 UAP1L1 PHF3 SCAPER

Mapping the Ku Interactome Using Proximity-Dependent Biotin Identification in Human Cells.

ZNF830 MYH10 SF3B1 PHF3 UTP14A SUPT16H

NDR2 acts as the upstream kinase of ARK5 during insulin-like growth factor-1 signaling.

NUAK1 STK38L

Biochemical characterisation of the proteins encoded by the DiGeorge critical region 6 (DGCR6) genes.

DGCR6 DGCR6L

Dysregulation of DGCR6 and DGCR6L: psychopathological outcomes in chromosome 22q11.2 deletion syndrome.

DGCR6 DGCR6L

A mouse gene (Dgcr6) related to the Drosophila gonadal gene is expressed in early embryogenesis and is the homolog of a human gene deleted in DiGeorge syndrome.

DGCR6 DGCR6L

Two functional copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus.

DGCR6 DGCR6L

Prediction of the coding sequences of mouse homologues of KIAA gene: III. the complete nucleotide sequences of 500 mouse KIAA-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries.

CUL3 DHX36 ICE1 RBM12 AGAP9 NUAK1 SUPT6H

Genome-wide CRISPR-Cas9 Screen Identifies Leukemia-Specific Dependence on a Pre-mRNA Metabolic Pathway Regulated by DCPS.

MYH10 SF3B1 PHF3 SUPT6H UTP14A SUPT16H

Isolation of a novel cDNA that encodes a protein localized to the pre-acrosome region of spermatids.

CEP131 UTP14A

Integration of cytogenetic with recombinational and physical maps of mouse chromosome 16.

DGCR6 DGCR6L

Targeting USP10 induces degradation of oncogenic ANLN in esophageal squamous cell carcinoma.

CUL3 DHX36 MYH10 SF3B1 TUBGCP2 ARGLU1 PHF3 UTP14A SUPT16H

Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders.

IQSEC1 CUL3 CEP131 MYH10 SF3B1 BRSK1 ARGLU1 SUPT16H

An antibody-based proximity labeling map reveals mechanisms of SARS-CoV-2 inhibition of antiviral immunity.

CEP131 ICE1 TUBGCP2 GOLGA5 TBC1D22A PHF3 NUCB2

Synthetic Lethal and Resistance Interactions with BET Bromodomain Inhibitors in Triple-Negative Breast Cancer.

CUL3 MSH3 RBM12 SF3B1 ARGLU1 PHF3 SUPT6H SUPT16H

MECP2 directly interacts with RNA polymerase II to modulate transcription in human neurons.

IQSEC1 DHX36 MYH10 SF3B1 ARGLU1 SUPT6H UTP14A SUPT16H

In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker.

FAM184B MYH10 SF3B1 RNF17 CCDC191 EML6 NUCB2 UTP14A SUPT16H

Fgf and Esrrb integrate epigenetic and transcriptional networks that regulate self-renewal of trophoblast stem cells.

ICE1 PHF3 UTP14A SUPT16H

Analysis of the Histone H3.1 Interactome: A Suitable Chaperone for the Right Event.

SF3B1 STK38L SUPT6H SUPT16H

Comprehensive interactome profiling of the human Hsp70 network highlights functional differentiation of J domains.

FAM184B CEP131 SF3B1 GOLGA5 ARGLU1 SUPT6H NUCB2 UTP14A SUPT16H

MKRN2 Physically Interacts with GLE1 to Regulate mRNA Export and Zebrafish Retinal Development.

MYH10 SF3B1 RNF17 SUPT6H SUPT16H

SR protein kinases promote splicing of nonconsensus introns.

CUL3 ICE1 SF3B1 RASGRF1 PHF3

Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.

DGCR6 DGCR6L

TRIM28 protects TRIM24 from SPOP-mediated degradation and promotes prostate cancer progression.

SUPT6H SUPT16H

Transcription factor Foxp3 and its protein partners form a complex regulatory network.

CUL3 DHX36 TUBGCP2 PHF3 UTP14A

Identification and sequencing the juvenile spermatogonial depletion critical interval on mouse chromosome 1 reveals the presence of eight candidate genes.

CUL3 UTP14A

TNIP2 is a Hub Protein in the NF-κB Network with Both Protein and RNA Mediated Interactions.

CUL3 CEP131 MYH10 NUAK1 USP32 SUPT16H SCAPER

Genetic and Proteomic Interrogation of Lower Confidence Candidate Genes Reveals Signaling Networks in β-Catenin-Active Cancers.

DHX36 MYH10 SF3B1 ARGLU1 PHF3 WDR87 GPS2 UTP14A

LKB1 is a master kinase that activates 13 kinases of the AMPK subfamily, including MARK/PAR-1.

BRSK1 NUAK1

Functional proteomics establishes the interaction of SIRT7 with chromatin remodeling complexes and expands its role in regulation of RNA polymerase I transcription.

DHX36 MYH10 SF3B1 PHF3 SUPT6H UTP14A

Comprehensive Interactome Mapping of the DNA Repair Scaffold SLX4 Using Proximity Labeling and Affinity Purification.

IQSEC1 MSH3 SUPT6H SUPT16H

The Nse5/6-like SIMC1-SLF2 complex localizes SMC5/6 to viral replication centers.

ZNF830 ICE1 SF3B1 ARGLU1 PHF3 UTP14A SUPT16H

MYC multimers shield stalled replication forks from RNA polymerase.

DHX36 MYH10 SF3B1 PHF3 SUPT6H UTP14A SUPT16H

The contribution of de novo coding mutations to autism spectrum disorder.

MYH10 PHF3

Jumonji modulates polycomb activity and self-renewal versus differentiation of stem cells.

ICE1 STK38L

Defining the human deubiquitinating enzyme interaction landscape.

CUL3 ICE1 MYH10 TUBGCP2 SUPT6H USP32 SUPT16H

p130Cas mediates the transforming properties of the anaplastic lymphoma kinase.

MYH10 TUBGCP2

Proteomic and Biochemical Comparison of the Cellular Interaction Partners of Human VPS33A and VPS33B.

DHX36 CEP131 TUBGCP2 GOLGA5

Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.

DGCR6 DGCR6L

SNIP1 Recruits TET2 to Regulate c-MYC Target Genes and Cellular DNA Damage Response.

SF3B1 ARGLU1 UTP14A SUPT16H

Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.

RAB11FIP4 BRSK1 GPS2

The E3 ubiquitin ligase HECTD1 contributes to cell proliferation through an effect on mitosis.

CUL3 DHX36 PHF3 UTP14A SUPT16H SCAPER

KCTD13-mediated ubiquitination and degradation of GluN1 regulates excitatory synaptic transmission and seizure susceptibility.

IQSEC1 CUL3 DHX36 MYH10 SF3B1 BRSK1 ARGLU1 SCAPER

Synaptic GAP and GEF Complexes Cluster Proteins Essential for GTP Signaling.

IQSEC1 CUL3 AGAP9 PHF3

The HECT type ubiquitin ligase NEDL2 is degraded by anaphase-promoting complex/cyclosome (APC/C)-Cdh1, and its tight regulation maintains the metaphase to anaphase transition.

DHX36 TUBGCP2 PHF3 SCAPER

Physiological and pathophysiological characteristics of ataxin-3 isoforms.

LAMA4 MYH10 SF3B1 WDR87

Neural tube defects by NUAK1 and NUAK2 double mutation.

MYH10 NUAK1

Elongin A regulates transcription in vivo through enhanced RNA polymerase processivity.

SUPT6H SUPT16H

The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts.

DHX36 RBM12 SF3B1 SUPT6H UTP14A SUPT16H

TRRAP is essential for regulating the accumulation of mutant and wild-type p53 in lymphoma.

SF3B1 TUBGCP2

Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region.

DGCR6 DGCR6L

Identification of 14-3-3epsilon substrates from embryonic murine brain.

CEP131 BRSK1 NUAK1

Robust phosphoproteomic profiling of tyrosine phosphorylation sites from human T cells using immobilized metal affinity chromatography and tandem mass spectrometry.

DHX36 RBM12 GOLGA5

14-3-3 cooperates with LKB1 to regulate the activity and localization of QSK and SIK.

BRSK1 NUAK1

Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization.

DGCR6 DGCR6L

Isolation and characterization of proteins associated with histone H3 tails in vivo.

SF3B1 SUPT16H

BTB-ZF factors recruit the E3 ligase cullin 3 to regulate lymphoid effector programs.

CUL3 SF3B1

STK11 is required for the normal program of ciliated cell differentiation in airways.

BRSK1 NUAK1

Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2.

DGCR6 DGCR6L

PRP19 transforms into a sensor of RPA-ssDNA after DNA damage and drives ATR activation via a ubiquitin-mediated circuitry.

DHX36 MYH10 MSH3 SF3B1

Menin and Menin-Associated Proteins Coregulate Cancer Energy Metabolism.

DHX36 MYH10 TUBGCP2 SUPT16H

SHLD2/FAM35A co-operates with REV7 to coordinate DNA double-strand break repair pathway choice.

CUL3 MSH3 UTP14A

LCP1 preferentially binds clasped αMβ2 integrin and attenuates leukocyte adhesion under flow.

DHX36 MYH10 SF3B1 SUPT16H

CHD3 and CHD4 form distinct NuRD complexes with different yet overlapping functionality.

MYH10 SF3B1 SUPT6H UTP14A SUPT16H

Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2.

DGCR6 DGCR6L

Large-scale mapping of human protein-protein interactions by mass spectrometry.

DHX36 MYH10 SF3B1 NUAK1 STK38L GPS2 GAS8

Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease.

MSH3 DGCR6 RAB11FIP4 SF3B1 ARGLU1 UAP1L1 USP32

N-Terminal Acetyltransferase Naa40p Whereabouts Put into N-Terminal Proteoform Perspective.

ICE1 MYH10 RBM12 SF3B1 GOLGA5 UTP14A

H4K20me0 recognition by BRCA1-BARD1 directs homologous recombination to sister chromatids.

MSH3 SF3B1 ARGLU1 PHF3 SUPT6H GPS2 SUPT16H

A bead-based approach for large-scale identification of in vitro kinase substrates.

SF3B1 SUPT6H UTP14A

A protein interaction landscape of breast cancer.

MYH10 MSH3 NUAK1 NUCB2 SUPT16H

The Hsp70-Hsp90 co-chaperone Hop/Stip1 shifts the proteostatic balance from folding towards degradation.

MYH10 SF3B1 TUBGCP2 SUPT6H SUPT16H

BAP1 regulation of the key adaptor protein NCoR1 is critical for γ-globin gene repression.

IQSEC1 DHX36 MYH10 SF3B1 ARGLU1 UTP14A SUPT16H

Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.

DGCR6 DGCR6L

MYH10 SF3B1 NUAK1 ARGLU1 PHF3 SUPT6H UTP14A SUPT16H

CUL3 LAMA4 DHX36 PHF3 SUPT6H UTP14A SUPT16H

RAB11FIP4 SUPT6H RSKR

MYH10 GPS2

RAB11FIP4 SUPT6H RSKR

RAB11FIP4 USP32 NUCB2

AGAP9 RASGRF1

DGCR6 DGCR6L

DGCR6 DGCR6L

GMEB1 SF3B1 TBC1D22A PHF3 GAS8

MYH10 RBM12 SF3B1 PHF3 SCAPER

GMEB1 MSH3 TUBGCP2 STK38L SCAPER

IQSEC1 UAP1L1 PHF3 SUPT6H SCAPER

IQSEC1 TBC1D22A PHF3 SUPT6H SCAPER

IQSEC1 CUL3 LAMA4 MSH3 TUBGCP2

GMEB1 TUBGCP2 STK38L TBC1D22A UTP14A

DGCR6 DGCR6L

CEP131 SCAPER

DGCR6 DGCR6L

AGAP9

206

ARGLU1

226

GPS2

21

DGCR6

126

CAVIN4

51

RBM12

616

RAB11FIP4

376

MSH3

716

GMEB1

546

GOLGA5

466

IQSEC1

861

FAM184B

851

RSKR

226

GOLGA6L22

316

TUBGCP2

406

NUCB2

291

ICE1

476

DHX36

81

CUL3

236

CCDC191

246

DGCR6L

126

BRSK1

336

EML6

396

SCAPER

751

CEP131

841

MYH10

871

MYH10

1851

LAMA4

516

STK38L

126

NUAK1

91

SUPT16H

201

RASGRF1

421

RNF17

171

SUPT6H

856

SF3B1

156

UAP1L1

236

PHF3

1031

UTP14A

581

VAT1L

356

TBC1D22A

391

ZNF830

226

SLC9C2

786

WDR87

1336

USP32

111

GAS8

26

GAS8

81