Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionmetalloendopeptidase activity

PHEX MBTPS1 ADAMTS16 MMP8 MMP12

1.21e-04120805GO:0004222
GeneOntologyMolecularFunctionpiRNA binding

PIWIL4 PIWIL3

2.35e-046802GO:0034584
GeneOntologyMolecularFunctionendopeptidase activity

PHEX HGF MBTPS1 USP9X ADAMTS16 NLRP1 MMP8 MMP12

3.24e-04430808GO:0004175
MousePhenoabnormal pelvic girdle joint morphology

PHEX COMP IDUA

7.54e-069643MP:0030819
MousePhenoabnormal hip joint morphology

PHEX COMP IDUA

7.54e-069643MP:0030829
MousePhenoabnormal girdle joint morphology

PHEX COMP IDUA

3.21e-0514643MP:0030818
MousePhenoabnormal hindlimb joint morphology

PHEX COMP IDUA

9.87e-0520643MP:0030808
MousePhenospiral ligament degeneration

HGF IDUA

1.23e-044642MP:0004864
DomainThbs/COMP_coiled-coil

THBS3 THBS4 COMP

7.57e-083803IPR024665
DomainCOMP

THBS3 THBS4 COMP

7.57e-083803PF11598
DomainTSP_3

THBS3 THBS4 COMP

7.52e-075803PF02412
DomainTSP3

THBS3 THBS4 COMP

7.52e-075803PS51234
DomainTSP_CTER

THBS3 THBS4 COMP

7.52e-075803PS51236
Domain-

THBS3 THBS4 COMP

7.52e-0758034.10.1080.10
DomainThrombospondin_C

THBS3 THBS4 COMP

7.52e-075803IPR008859
DomainTSP_C

THBS3 THBS4 COMP

7.52e-075803PF05735
DomainThrombospondin_3_rpt

THBS3 THBS4 COMP

7.52e-075803IPR017897
DomainThrombospondin_3-like_rpt

THBS3 THBS4 COMP

7.52e-075803IPR003367
DomainTSP_type-3_rpt

THBS3 THBS4 COMP

7.52e-075803IPR028974
DomainIon_trans_dom

TRPM6 CACNA1F SCN11A KCNQ5 CNGA1

1.30e-04114805IPR005821
DomainIon_trans

TRPM6 CACNA1F SCN11A KCNQ5 CNGA1

1.30e-04114805PF00520
DomainMetalloPept_cat_dom

PHEX ADAMTS16 MMP8 MMP12

4.04e-0481804IPR024079
Domain-

PHEX ADAMTS16 MMP8 MMP12

4.04e-04818043.40.390.10
DomainPIWI

PIWIL4 PIWIL3

4.99e-048802PS50822
DomainPiwi

PIWIL4 PIWIL3

4.99e-048802SM00950
DomainPiwi

PIWIL4 PIWIL3

4.99e-048802IPR003165
DomainPiwi

PIWIL4 PIWIL3

4.99e-048802PF02171
DomainPAZ

PIWIL4 PIWIL3

6.40e-049802PS50821
DomainPAZ

PIWIL4 PIWIL3

6.40e-049802SM00949
DomainPAZ_dom

PIWIL4 PIWIL3

6.40e-049802IPR003100
DomainPAZ

PIWIL4 PIWIL3

6.40e-049802PF02170
DomainCYSTEINE_SWITCH

ADAMTS16 MMP8 MMP12

7.17e-0441803PS00546
DomainPept_M10_metallopeptidase

ADAMTS16 MMP8 MMP12

8.25e-0443803IPR001818
DomainZINC_PROTEASE

PHEX ADAMTS16 MMP8 MMP12

8.31e-0498804PS00142
DomainIMPORTIN_B_NT

XPO1 IPO11

1.59e-0314802PS50166
DomainPept_M10A_Zn_BS

MMP8 MMP12

1.83e-0315802IPR021158
DomainIBN_N

XPO1 IPO11

1.83e-0315802PF03810
DomainIBN_N

XPO1 IPO11

2.09e-0316802SM00913
DomainHemopexin_CS

MMP8 MMP12

2.36e-0317802IPR018486
DomainImportin-beta_N

XPO1 IPO11

2.36e-0317802IPR001494
DomainPept_M10A_stromelysin-type

MMP8 MMP12

2.65e-0318802IPR016293
DomainPG_binding_1

MMP8 MMP12

3.27e-0320802PF01471
DomainPeptidoglycan-bd-like

MMP8 MMP12

3.27e-0320802IPR002477
DomainHemopexin-like_dom

MMP8 MMP12

4.32e-0323802IPR000585
DomainTSPN

THBS3 THBS4

4.32e-0323802SM00210
DomainHemopexin-like_repeat

MMP8 MMP12

4.32e-0323802IPR018487
DomainM10A_MMP

MMP8 MMP12

4.32e-0323802IPR033739
DomainHemopexin

MMP8 MMP12

4.32e-0323802PF00045
DomainHEMOPEXIN

MMP8 MMP12

4.32e-0323802PS00024
Domain-

MMP8 MMP12

4.32e-03238022.110.10.10
DomainHEMOPEXIN_2

MMP8 MMP12

4.32e-0323802PS51642
Pubmed

Pathological Significance and Prognostic Roles of Thrombospondin-3, 4 and 5 in Bladder Cancer.

THBS3 THBS4 COMP

1.26e-08382333910854
Pubmed

Thrombospondin-3 augments injury-induced cardiomyopathy by intracellular integrin inhibition and sarcolemmal instability.

THBS3 THBS4 COMP

1.26e-07582330622267
Pubmed

Skeletal abnormalities in mice lacking extracellular matrix proteins, thrombospondin-1, thrombospondin-3, thrombospondin-5, and type IX collagen.

THBS3 THBS4 COMP

1.26e-07582318467703
Pubmed

Thrombospondins 1 and 2 are important for afferent synapse formation and function in the inner ear.

THBS3 THBS4 COMP

7.01e-07882324460873
Pubmed

Cell cycle-dependent phosphorylation regulates RECQL4 pathway choice and ubiquitination in DNA double-strand break repair.

KAT5 HDAC6 GTF3C1 PTCD1 DNAAF10 USP9X GYG1 WDR87 RECQL4 SF3A3 PCNX1 CHD3 XPO1 LANCL2

2.70e-061335821429229926
Pubmed

Quantitative mass spectrometry of diabetic kidney tubules identifies GRAP as a novel regulator of TGF-beta signaling.

GRAPL GRAP

5.49e-06282219836472
Pubmed

Grap negatively regulates T-cell receptor-elicited lymphocyte proliferation and interleukin-2 induction.

GRAPL GRAP

5.49e-06282211971956
Pubmed

Ubiquitin-specific protease activity of USP9Y, a male infertility gene on the Y chromosome.

USP9X USP9Y

5.49e-06282212895410
Pubmed

Cultured human retinal pigment epithelial cells differentially express thrombospondin-1, -2, -3, and -4.

THBS3 THBS4

5.49e-06282211137453
Pubmed

COMP and TSP-4 interact specifically with the novel GXKGHR motif only found in fibrillar collagens.

THBS4 COMP

5.49e-06282230464261
Pubmed

The Drosophila developmental gene fat facets has a human homologue in Xp11.4 which escapes X-inactivation and has related sequences on Yq11.2.

USP9X USP9Y

5.49e-0628228922996
Pubmed

Detection of Grb-2-related adaptor protein gene (GRAP) and peptide molecule in salivary glands of MRL/lpr mice and patients with Sjögren's syndrome.

GRAPL GRAP

5.49e-06282215174222
Pubmed

A CRM1-mediated nuclear export signal governs cytoplasmic localization of BRCA2 and is essential for centrosomal localization of BRCA2.

BRCA2 XPO1

5.49e-06282218059333
Pubmed

Usp9y (ubiquitin-specific protease 9 gene on the Y) is associated with a functional promoter and encodes an intact open reading frame homologous to Usp9x that is under selective constraint.

USP9X USP9Y

5.49e-06282212925892
Pubmed

Grb2-related adaptor protein GRAP is a novel regulator of liver fibrosis.

GRAPL GRAP

5.49e-06282237343720
Pubmed

TRIM68 regulates ligand-dependent transcription of androgen receptor in prostate cancer cells.

KAT5 TRIM68

1.64e-05382218451177
Pubmed

The small G protein Arf6 expressed in keratinocytes by HGF stimulation is a regulator for skin wound healing.

HGF ARF6

1.64e-05382228429746
Pubmed

HGF-induced migration depends on the PI(3,4,5)P3-binding microexon-spliced variant of the Arf6 exchange factor cytohesin-1.

HGF ARF6

1.64e-05382230404949
Pubmed

Hepatocyte growth factor attenuates high glucose-disturbed mitochondrial dynamics in podocytes by decreasing ARF6-dependent DRP1 translocation.

HGF ARF6

1.64e-05382237913847
Pubmed

Regulatory expression of MMP-8/MMP-9 and inhibition of proliferation, migration and invasion in human lung cancer A549 cells in the presence of HGF variants.

HGF MMP8

1.64e-05382224099107
Pubmed

Causal Effect of MMP-1 (Matrix Metalloproteinase-1), MMP-8, and MMP-12 Levels on Ischemic Stroke: A Mendelian Randomization Study.

MMP8 MMP12

1.64e-05382233902302
Pubmed

Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin-deficient mouse.

HDAC6 DYSF

1.64e-05382231218594
Pubmed

Histone deacetylase 6 (HDAC6) deacetylates survivin for its nuclear export in breast cancer.

HDAC6 XPO1

1.64e-05382222334690
Pubmed

Transgenically-expressed secretoglobin 3A2 accelerates resolution of bleomycin-induced pulmonary fibrosis in mice.

PLAAT1 BRCA2 XPO1

2.47e-052482326178733
Pubmed

Immunohistochemical localisation of thrombospondin in human megakaryocytes and platelets.

THBS3 THBS4

3.28e-0548226338048
Pubmed

Tip60 is required for DNA interstrand cross-link repair in the Fanconi anemia pathway.

KAT5 BRCA2

3.28e-05482218263878
Pubmed

TNF stimulates nuclear export and secretion of IL-15 by acting on CRM1 and ARF6.

XPO1 ARF6

3.28e-05482223950892
Pubmed

Possible role of HIWI2 in modulating tight junction proteins in retinal pigment epithelial cells through Akt signaling pathway.

PIWIL4 PIWIL3

3.28e-05482228025795
Pubmed

Genetic variants in Piwi-interacting RNA pathway genes confer susceptibility to spermatogenic failure in a Chinese population.

PIWIL4 PIWIL3

3.28e-05482220940137
Pubmed

Crucial role of the small GTPase ARF6 in hepatic cord formation during liver development.

HGF ARF6

3.28e-05482216880525
Pubmed

Global mapping of herpesvirus-host protein complexes reveals a transcription strategy for late genes.

GTF3C1 GLB1 USP9X SNX18 SF3A3 CHD3 USP9Y IPO11

3.81e-0553382825544563
Pubmed

Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss.

GRAPL GRAP

5.47e-05582230610177
Pubmed

A cancer-associated BRCA2 mutation reveals masked nuclear export signals controlling localization.

BRCA2 XPO1

5.47e-05582224013206
Pubmed

Fam65b is important for formation of the HDAC6-dysferlin protein complex during myogenic cell differentiation.

HDAC6 DYSF

5.47e-05582224687993
Pubmed

Matrix metalloproteinase polymorphisms and bladder cancer risk.

MMP8 MMP12

8.19e-05682217178858
Pubmed

Requirement for p62 acetylation in the aggregation of ubiquitylated proteins under nutrient stress.

KAT5 HDAC6

8.19e-05682231857589
Pubmed

Matrix metalloproteinase activity in pediatric acute lung injury.

MMP8 MMP12

8.19e-05682219159011
Pubmed

Matrix metalloproteinase polymorphisms are associated with bladder cancer invasiveness.

MMP8 MMP12

8.19e-05682217473191
Pubmed

Interferon gamma receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infection.

IFNGR2 MMP8 MMP12

8.53e-053682320587546
Pubmed

Fine physical mapping of the human matrix metalloproteinase genes clustered on chromosome 11q22.3.

MMP8 MMP12

1.14e-0478228921407
Pubmed

Two distinct tyrosine-based motifs enable the inhibitory receptor FcgammaRIIB to cooperatively recruit the inositol phosphatases SHIP1/2 and the adapters Grb2/Grap.

GRAPL GRAP

1.14e-04782215456754
Pubmed

Matrix metalloproteinases cleave tissue factor pathway inhibitor. Effects on coagulation.

MMP8 MMP12

1.14e-04782210859319
Pubmed

Identification and enzymatic characterization of two diverging murine counterparts of human interstitial collagenase (MMP-1) expressed at sites of embryo implantation.

MMP8 MMP12

1.14e-04782211113146
Pubmed

The cytoskeleton-associated protein SCHIP1 is involved in axon guidance, and is required for piriform cortex and anterior commissure development.

L1CAM MOG

1.52e-04882225953347
Pubmed

TRIM68 negatively regulates IFN-β production by degrading TRK fused gene, a novel driver of IFN-β downstream of anti-viral detection systems.

NLRP1 TRIM68

1.52e-04882224999993
Pubmed

FBXO22 promotes leukemogenesis by targeting BACH1 in MLL-rearranged acute myeloid leukemia.

CRNKL1 GTF3C1 USP9X XPO1 USP9Y DYSF IPO11

1.76e-0449782736774506
Pubmed

HiPLA: High-throughput imaging proximity ligation assay.

HDAC6 BRCA2 CHD3

1.78e-044682330419336
Pubmed

Identification of eight members of the Argonaute family in the human genome.

PIWIL4 PIWIL3

1.96e-04982212906857
Pubmed

A function for cyclin D1 in DNA repair uncovered by protein interactome analyses in human cancers.

GTF3C1 BRCA2 XPO1 ARF6

2.24e-0412582421654808
Pubmed

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

CRNKL1 KAT5 HDAC6 WIZ GTF3C1 HECTD4 SF3A3 XPO1 USP9Y SIPA1L2

2.29e-041082821038697112
Pubmed

Biochemical and genetic evidence for a role of IGHMBP2 in the translational machinery.

GTF3C1 ABT1

2.44e-041082219299493
Pubmed

Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene.

USP9X USP9Y

2.44e-04108229384609
Pubmed

Tcf20 deficiency is associated with increased liver fibrogenesis and alterations in mitochondrial metabolism in mice and humans.

MMP8 MMP12

2.98e-041182237312667
Pubmed

FACT-mediated exchange of histone variant H2AX regulated by phosphorylation of H2AX and ADP-ribosylation of Spt16.

KAT5 BRCA2

2.98e-041182218406329
Pubmed

Peripheral nervous system defects in erbB2 mutants following genetic rescue of heart development.

SLC18A3 L1CAM

2.98e-041182210521398
Pubmed

Structural differences of matrix metalloproteinases. Homology modeling and energy minimization of enzyme-substrate complexes.

MMP8 MMP12

2.98e-041182210949161
Pubmed

A directed protein interaction network for investigating intracellular signal transduction.

CRNKL1 MBTPS1 KAT5 HDAC6 WIZ GTF3C1 GLB1 ENTPD6 ZFP28 CHD3

3.10e-041124821021900206
Pubmed

Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis.

USP9X USP9Y

3.57e-041282223861879
Pubmed

Ubiquitin-specific peptidase 9, X-linked (USP9X) modulates activity of mammalian target of rapamycin (mTOR).

MAGED4 USP9X

3.57e-041282222544753
Pubmed

A role for Nr-CAM in the patterning of binocular visual pathways.

L1CAM CNTN3

3.57e-041282216701205
Pubmed

Blimp1 regulates the transition of neonatal to adult intestinal epithelium.

GLB1 PRDM1

4.21e-041382221878906
Pubmed

Pioneering axons regulate neuronal polarization in the developing cerebral cortex.

L1CAM CNTN3

4.21e-041382224559674
Pubmed

Systematic screening reveals a role for BRCA1 in the response to transcription-associated DNA damage.

HGF KAT5 WIZ BRCA2

4.37e-0414982425184681
Pubmed

Evidence for the interaction of the regulatory protein Ki-1/57 with p53 and its interacting proteins.

KAT5 CHD3

4.91e-041482216455055
Pubmed

Dysregulation of TGF-beta1 receptor activation leads to abnormal lung development and emphysema-like phenotype in core fucose-deficient mice.

MMP8 MMP12

4.91e-041482216236725
Pubmed

Metalloproteinases promote plaque rupture and myocardial infarction: A persuasive concept waiting for clinical translation.

MMP8 MMP12

4.91e-041482225636537
Pubmed

Deubiquitinating enzymes: a new class of biological regulators.

USP9X USP9Y

5.65e-04158229827704
Pubmed

Identification of SH3 domain proteins interacting with the cytoplasmic tail of the a disintegrin and metalloprotease 10 (ADAM10).

SNX18 GRAP

5.65e-041582225036101
Pubmed

Evolutionary strata on the mouse X chromosome correspond to strata on the human X chromosome.

USP9X USP9Y

5.65e-041582214762062
Pubmed

Association of matrix metalloproteinase gene polymorphisms with refractive error in Amish and Ashkenazi families.

MMP8 MMP12

6.45e-041682220484597
Pubmed

Matrix metalloproteinases in tumor invasion.

MMP8 MMP12

6.45e-041682210949577
Pubmed

Expression dynamics of metalloproteinases during mandibular bone formation: association with Myb transcription factor.

MMP8 MMP12

6.45e-041682237701782
Pubmed

Protein interaction network of the mammalian Hippo pathway reveals mechanisms of kinase-phosphatase interactions.

HDAC6 DNAAF10 USP9X SNX18 SIPA1L2 IPO11

6.62e-0444682624255178
Pubmed

Fibulin-1 regulates the pathogenesis of tissue remodeling in respiratory diseases.

MMP8 MMP12

7.30e-041782227398409
Pubmed

A high-resolution 6.0-megabase transcript map of the type 2 diabetes susceptibility region on human chromosome 20.

ACOT8 DNAAF9

7.30e-041782211549316
Pubmed

A strategy for modulation of enzymes in the ubiquitin system.

USP9X USP9Y

7.30e-041782223287719
Pubmed

R2TP/Prefoldin-like component RUVBL1/RUVBL2 directly interacts with ZNHIT2 to regulate assembly of U5 small nuclear ribonucleoprotein.

CRNKL1 DNAAF10 USP9X SF3A3 IPO11

7.33e-0430082528561026
Pubmed

Deletion of STK40 protein in mice causes respiratory failure and death at birth.

HGF TTF1

8.20e-041882223293024
Pubmed

Sex differences in sex chromosome gene expression in mouse brain.

USP9X USP9Y

8.20e-041882212023983
Pubmed

Combinatorial targeting of a chromatin complex comprising Dot1L, menin and the tyrosine kinase BAZ1B reveals a new therapeutic vulnerability of endocrine therapy-resistant breast cancer.

CRNKL1 WIZ GTF3C1 SF3A3 ABT1 CHD3 XPO1 NDUFB5

8.72e-0484782835850772
Pubmed

A new transcriptional role for matrix metalloproteinase-12 in antiviral immunity.

MMP8 MMP12

9.15e-041982224784232
Pubmed

ATXN1 protein family and CIC regulate extracellular matrix remodeling and lung alveolarization.

MMP8 MMP12

9.15e-041982222014525
Pubmed

Expression analysis of the entire MMP and TIMP gene families during mouse tissue development.

MMP8 MMP12

9.15e-041982215063736
Pubmed

In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.

HGD THBS4 COMP GLB1 SNX18 STEAP4 IDUA DYSF ARF6

9.37e-04107082923533145
Pubmed

Characterization of the EGFR interactome reveals associated protein complex networks and intracellular receptor dynamics.

USP9X XPO1 LANCL2 IPO11

9.42e-0418382423956138
Pubmed

A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM).

IFNGR2 THBS4 MMP8 MMP12

1.00e-0318682420673868
Pubmed

Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes.

IFNGR2 THBS4 MMP8 MMP12

1.00e-0318682420452482
Pubmed

Prefrontal cortex shotgun proteome analysis reveals altered calcium homeostasis and immune system imbalance in schizophrenia.

L1CAM LANCL2 MOG

1.05e-038482319165527
Pubmed

The transcriptional repressor Blimp1/Prdm1 regulates postnatal reprogramming of intestinal enterocytes.

GLB1 PRDM1

1.12e-032182221670299
Pubmed

Prohibitin regulates TGF-beta induced apoptosis as a downstream effector of Smad-dependent and -independent signaling.

GTF3C1 IPO11

1.12e-032182219725029
Pubmed

Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2.

BRCA2 XPO1 USP9Y

1.16e-038782317148452
Pubmed

Cartilage-specific ablation of site-1 protease in mice results in the endoplasmic reticulum entrapment of type IIb procollagen and down-regulation of cholesterol and lipid homeostasis.

MBTPS1 COMP

1.23e-032282225147951
Pubmed

Functional interactions between matrix metalloproteinases and glycosaminoglycans.

MMP8 MMP12

1.23e-032282223421805
Pubmed

Matrix metalloproteinases.

MMP8 MMP12

1.23e-032282210419448
Pubmed

Decreased expression levels of Ifi genes is associated to the increased resistance to spontaneous arthritis disease in mice deficiency of IL-1RA.

CHST10 KCNQ5 DNAAF10 SNX18

1.26e-0319882427480124
Pubmed

Menin and Menin-Associated Proteins Coregulate Cancer Energy Metabolism.

CRNKL1 WIZ GTF3C1 CHD3 IPO11

1.30e-0334182532971831
Pubmed

MRG15 binds directly to PALB2 and stimulates homology-directed repair of chromosomal breaks.

KAT5 BRCA2

1.35e-032382220332121
Pubmed

Matrix metalloproteinases 2 and 9 are dispensable for pancreatic islet formation and function in vivo.

MMP8 MMP12

1.47e-032482215734845
Pubmed

Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects.

THBS3 THBS4 COMP ADAMTS16

1.56e-0321082416537572
Pubmed

Symmetric neural progenitor divisions require chromatin-mediated homologous recombination DNA repair by Ino80.

BRCA2 L1CAM

1.59e-032582232737294
GeneFamilyArgonaute/PIWI family

PIWIL4 PIWIL3

3.20e-048622408
ToppCellClub_cells-SSc-ILD_02|World / lung cells shred on cell class, cell subclass, sample id

THBS4 WIZ STEAP4 CNTN3 SLC13A3 CNGA1

3.37e-071478369211242a8e40d50414d310940616eccce299a7f8
ToppCellrenal_medulla_nuclei-Renal_AKI_(acute_kidney_injury)-Endothelial-blood_vessel_endothelial_cell_of_kidney-capillary-immature_endothelial_cell-Glomerular_Capillary_Endothelial_Cell|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group

KCNQ5 WDR87 NLRP1 RXFP1 DYSF PRDM1

5.34e-07159836d3f81ba22160568ccaa6d2b04ebfd30630f9a6db
ToppCellMesenchymal_cells-Fibro/Chondro_p.|Mesenchymal_cells / Lineage and Cell class

THBS4 PLAAT1 KCNQ5 COMP COLGALT2 DYSF

1.76e-06195836b95a631d54c6cf85e48e1e638703206aaaebc073
ToppCellrenal_medulla_nuclei-CKD+DKD_normotensive-Epithelial-Distal_tubule_epithelial_cell-kidney_distal_convoluted_tubule_epithelial_cell|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

TRPM6 ADAMTS16 ANKLE1 B4GALNT3 ABCA10

6.49e-061408355e81fa3a19d23f0e9cae3878431ca1f78dff7238
ToppCellCOVID-19-APC-like-Monocyte-derived_macrophages|COVID-19 / group, cell type (main and fine annotations)

CRNKL1 DNAAF10 GYG1 PIWIL4 LANCL2

1.52e-05167835854a5dbd43f2b25825a71d37fd7779507783a99a
ToppCellhealthy_donor-Myeloid-Monocytic-Neutrophil|healthy_donor / Disease condition, Lineage, Cell class and subclass

TRPM6 PLAAT1 AOC3 STEAP4 DYSF

1.57e-0516883504259f5a9b067cd1b5619e34591e4b2fccc18535
ToppCelldroplet-Fat-Mat-18m-Hematologic-monocyte|Fat / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

HGF KCNQ5 L1CAM CHD3 LANCL2

1.96e-05176835867936a20f73f638055c19c8d88834aa2cc657cf
ToppCell367C-Endothelial_cells-Endothelial-F_(Lymphatics)-|367C / Donor, Lineage, Cell class and subclass (all cells)

THBS4 GRAPL DYSF IPO11 GRAP

2.25e-05181835b244ecaa442bbef51289d8ec574ef08fa9e96318
ToppCell367C-Endothelial_cells-Endothelial-F_(Lymphatics)|367C / Donor, Lineage, Cell class and subclass (all cells)

THBS4 GRAPL DYSF IPO11 GRAP

2.25e-05181835dd79de8098edb385a0f85d0e9621503cdf76ec43
ToppCellrenal_papilla_nuclei-Hypertensive_with+without-CKD-Endothelial-blood_vessel_endothelial_cell_of_kidney-capillary-immature_endothelial_cell-Peritubular_Capilary_Endothelial_Cell_|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

TRPM6 GRAPL DYSF GRAP PRDM1

2.37e-05183835dc19857b66dcadbf7c87de91f7b1f4e8ef2857ed
ToppCellrenal_papilla_nuclei-Hypertensive_with+without-CKD-Endothelial-blood_vessel_endothelial_cell_of_kidney-capillary-immature_endothelial_cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

TRPM6 GRAPL DYSF GRAP PRDM1

2.37e-051838354759560e5b4f4e5a00e5f933e3451a27c7c4aefe
ToppCellControl-Myeloid-MoAM1|Control / Disease group,lineage and cell class (2021.01.30)

HGF COLGALT2 MMP12 DYSF PRDM1

2.76e-0518983555d5c2fb9e6ab556d42c83a1e985ee66e4cf9dba
ToppCellBAL-Control-Myeloid-MoAM-MoAM1|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.09)

HGF COLGALT2 MMP12 DYSF PRDM1

2.76e-05189835ebb5e069fdca7cf8ffac16a57572e92d2593c86a
ToppCellBAL-Control-Myeloid-MoAM-MoAM1-|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.09)

HGF COLGALT2 MMP12 DYSF PRDM1

2.76e-05189835a59e4eaff430a443f9fa7edabe64e66a15b6bffb
ToppCellBAL-Control-Myeloid-MoAM-MoAM1-|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

HGF COLGALT2 MMP12 DYSF PRDM1

2.83e-051908355c8aa310886c64ee5dce4ba46a3dd178da549529
ToppCellBAL-Control-Myeloid-MoAM-MoAM1|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

HGF COLGALT2 MMP12 DYSF PRDM1

2.83e-051908354b4fe93061c87605dddf5bec94fa07c749c722aa
ToppCellStriatum-Endothelial-MURAL-M1(Rgs5Acta2)-M1_3-MURAL_Mural.Rgs5Acta2.Ccnd1_(Mural.Rgs5Acta2.Ccnd1)|Striatum / BrainAtlas - Mouse McCarroll V32

CACNA1F COMP AOC3 STEAP4

3.14e-0596834d98df92856840602a82d3f050bf0a1543445cac0
ToppCellStriatum-Endothelial-MURAL-M1(Rgs5Acta2)-M1_3-MURAL_Mural.Rgs5Acta2.Ccnd1_(Mural.Rgs5Acta2.Ccnd1)-|Striatum / BrainAtlas - Mouse McCarroll V32

CACNA1F COMP AOC3 STEAP4

3.14e-0596834bf62c29da66aa3eefdc59337dfb3cd0467f04f10
ToppCellCOVID_vent-Myeloid-Monocytic-Developing_Neutrophil|COVID_vent / Disease condition, Lineage, Cell class and subclass

TRPM6 PIWIL4 B4GALNT3 MMP8 DYSF

3.21e-05195835de23409b1b4146b8ae286850b829ec8dceed0117
Drugchondroitin sulfate

HGF CHST10 THBS3 THBS4 COMP GLB1 L1CAM ADAMTS16 B4GALNT3 MMP8 IDUA MOG

2.85e-084138212CID000024766
DiseaseOligospermia

PIWIL4 PIWIL3

4.83e-0412812C0028960
DiseaseSpastic Paraplegia, Hereditary

L1CAM CYP2U1

6.63e-0414812C0037773
Diseasethoracic aortic aneurysm (is_marker_for)

MMP8 MMP12

6.63e-0414812DOID:14004 (is_marker_for)
DiseaseMyasthenic Syndromes, Congenital, Slow Channel

DPAGT1 SLC18A3

8.71e-0416812C0751885
Diseaserheumatoid arthritis (is_marker_for)

HGF MMP8 CCL22

9.16e-0469813DOID:7148 (is_marker_for)
DiseaseCongenital Myasthenic Syndromes, Postsynaptic

DPAGT1 SLC18A3

9.85e-0417812C0751883
DiseaseCongenital Myasthenic Syndromes, Presynaptic

DPAGT1 SLC18A3

1.23e-0319812C0751884
Diseasesmall cell lung carcinoma

BRCA2 PIWIL4 ABT1

1.41e-0380813EFO_0000702
DiseaseArthrogryposis

SLC18A3 L1CAM

1.51e-0321812C0003886
Diseasevitiligo (is_implicated_in)

HGF NLRP1

1.51e-0321812DOID:12306 (is_implicated_in)
Diseaseotitis media (implicated_via_orthology)

PHEX IDUA

1.66e-0322812DOID:10754 (implicated_via_orthology)
DiseaseMyasthenic Syndromes, Congenital

DPAGT1 SLC18A3

1.98e-0324812C0751882

Protein segments in the cluster

PeptideGeneStartEntry
HIGRNIARPWKLIYY

TTF1

591

Q15361
LFRGRHYWVPAKRLF

ACOT8

41

O14734
VRYRLPLRVVKHFYW

CCL22

41

O00626
YVGKGTRARPYVHLW

ANKLE1

486

Q8NAG6
YRLKFNWGYRIPVIK

ABCA10

46

Q8WWZ4
PKWTNYGLRIFGYLH

B4GALNT3

161

Q6L9W6
SYRWFLQHRPQVGYI

COMP

681

P49747
NYIRVKPHPWYSGRI

GRAPL

51

Q8TC17
NYIRVKPHPWYSGRI

GRAP

51

Q13588
YWQMVRPFLKPGYRH

CFAP46

136

Q8IYW2
NSRRFRGRHYKWKPY

ADAMTS16

656

Q8TE57
PARWTIQKVFYQGRY

AOC3

256

Q16853
LFFKDRYFWRRHPQL

MMP8

296

P22894
YGEALHRILGYRWKI

MSANTD5

116

A0A3B3IT52
GPVWRKHYITYRINN

MMP12

106

P39900
WNKYQPLDHVRRYFG

ANO7

326

Q6IWH7
RRYIPKNPHQYRVWA

CACNA1F

1171

O60840
IYVVQRRWNYGIHPS

ANOS1

216

P23352
RIPFAFWARYHQYIL

MAGED4

671

Q96JG8
KRVLWDQYHNLRYPP

MBTPS1

621

Q14703
LAVLYFKHGIDRYWR

IPO11

61

Q9UI26
YNVLERPRGWAFIYH

KCNQ5

116

Q9NR82
ELGRHRLKPWYFSPY

KAT5

236

Q92993
ERCPLLYQWHRKQYV

LANCL2

246

Q9NS86
HYSRVPRFYWKDRLL

GLB1

56

P16278
AGGLHLWKYEYPIQR

DNAAF10

281

Q96MX6
LGLLYHNWYPSRVFV

DPAGT1

236

Q9H3H5
AAQKVKHYYRFWILP

PCNX1

966

Q96RV3
KHYYRFWILPQLWIG

PCNX1

971

Q96RV3
NLYRVHFPVAGSYRW

NLRP1

1096

Q9C000
VKGHLRGYNVTYWRE

L1CAM

841

P32004
NRPGIFVRVAYYAKW

HGF

701

P14210
YKAPWARVLVYGLGH

HECTD4

2611

Q9Y4D8
VGWYRPPFSRVVHLY

MOG

66

Q16653
VFAHYGPVWRQQRKF

CYP2U1

166

Q7Z449
SPFRYDLWNLKYLHR

ABT1

136

Q9ULW3
VPPIQEKRHWKRYIY

CRNKL1

521

Q9BZJ0
VHFLGRVKPWNYTYD

GYG1

211

P46976
DPKLISRIWVYNHYR

BRCA2

2611

P51587
YYRFGIKPEWMTVHR

CHD3

621

Q12873
PVNFRYLLPYVAHWR

DNAAF9

111

Q5TEA3
RRYIGRYGLAHVSKW

IDUA

161

P35475
LKYRGLIKYWFHTPP

IFNGR2

271

P38484
LYFSIHRYEQGRFWP

HDAC6

271

Q9UBN7
LKNVQRLYHYVEWRP

COLGALT2

106

Q8IYK4
HFRVISRPQWVAYKY

PIWIL3

131

Q7Z3Z3
YRRNIWKGFLISIPY

SLC13A3

226

Q8WWT9
GTIYREPRHAYLRKW

DYSF

306

O75923
NVARGRLTYYAKPHW

CNTN3

306

Q9P232
RWGVADKTFRPPYYH

HGD

321

Q93099
ASRLQYYVPRGFWKQ

USP9X

1656

Q93008
VRLAARYPHLQWLYG

SLC18A3

346

Q16572
VGVFIYVAYIKWHRA

ENTPD6

51

O75354
VYGQDRRFWRKYLHL

RECQL4

1176

O94761
RLTFKLCHLYYNWPG

PIWIL4

801

Q7Z3Z4
YKYRFVPWIALNLSH

SETD9

16

Q8NE22
PYHRQGAVNKYVIGW

SIPA1L2

1386

Q9P2F8
NRKYFWRIYSRGELH

PRDM1

131

O75626
WIKHRPQKVGAYRSY

WIZ

1441

O95785
VRQLWHEGPQYFYRG

SLC25A53

66

Q5H9E4
YQKRLRFYWRPHCRG

PLA2G2D

126

Q9UNK4
GQDKIRPLWRHYYTG

ARF6

66

P62330
RPLWRHYYTGTQGLI

ARF6

71

P62330
PWYRHEIAPGIIRKY

CHST10

211

O43529
YFKLGWNYPEIRLNR

CNGA1

256

P29973
YRWFLQHRPQVGYIR

THBS4

881

P35443
LIRHWRYYHTGEKPF

ZFP28

491

Q8NHY6
YIVGQYPRFLRAHWK

XPO1

546

O14980
YLSPHYGFWVIRLRK

TRIM68

386

Q6AZZ1
GHQHLPWTRKVYEFY

TRPM6

821

Q9BX84
QVPVHRRYKHFDWLY

SNX18

306

Q96RF0
WGHPKYTCLYRFRVH

SUN3

336

Q8TAQ9
EYYKHPISRWIARNF

NDUFB5

111

O43674
YGVYPWLRHNVDLKL

PHEX

101

P78562
RPFKEMIHRFWYNYR

RXFP1

686

Q9HBX9
YRGTKYRRFPDWLDH

STEAP4

271

Q687X5
LQYYVPRGFWKQFRL

USP9Y

1661

O00507
SYRWQLLHRPQVGYI

THBS3

876

P49746
IEVFRPGYQHWALYL

PLAAT1

21

Q9HDD0
LDPYHYFRRGWNIFD

SCN11A

631

Q9UI33
YRGPKAFQRHFAEWR

SF3A3

416

Q12874
KLWRRPITGTHLYQY

STARD7

151

Q9NQZ5
AWLRRGLYYLKAGQH

TTC37

566

Q6PGP7
GRRNTPYWYFLQCKH

PTCD1

131

O75127
RVVHMFLWYLIYGHP

GTF3C1

801

Q12789
ILRYYFGHGREWLFA

WDR87

766

Q6ZQQ6