Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctioncomplement component C3b binding

CFH CFHR5 CFHR3

3.82e-0612533GO:0001851
GeneOntologyMolecularFunctionopsonin binding

CFH CFHR5 CFHR3

3.90e-0525533GO:0001846
GeneOntologyMolecularFunctioncomplement binding

CFH CFHR5 CFHR3

8.29e-0532533GO:0001848
GeneOntologyMolecularFunctionfrizzled binding

WNT7B WNT9B WNT4

1.88e-0442533GO:0005109
GeneOntologyMolecularFunctiontumor necrosis factor receptor activity

TNFRSF11A TNFRSF4

4.49e-0412532GO:0005031
GeneOntologyMolecularFunctiontranscription coregulator activity

ZMYND11 ZNF366 AEBP2 WNT4 ZXDA ZNF541 RBCK1

6.76e-04562537GO:0003712
GeneOntologyMolecularFunctionglycosaminoglycan binding

CFH CCN6 LPA STAB1 CFHR3

7.12e-04268535GO:0005539
GeneOntologyMolecularFunctionsignaling receptor regulator activity

CCN6 WNT7B PDGFD WNT9B WNT4 IGSF1 TAFA2

1.16e-03616537GO:0030545
GeneOntologyMolecularFunctiondeath receptor activity

TNFRSF11A TNFRSF4

1.41e-0321532GO:0005035
GeneOntologyMolecularFunctionheparin binding

CFH CCN6 LPA CFHR3

1.68e-03192534GO:0008201
GeneOntologyBiologicalProcessmetanephric tubule development

WNT7B WNT9B WNT4

3.77e-0526523GO:0072170
GeneOntologyBiologicalProcesskidney development

CFH OVOL1 WNT7B PDGFD WNT9B WNT4 SMAD2

3.90e-05372527GO:0001822
GeneOntologyBiologicalProcessmetanephric epithelium development

WNT7B WNT9B WNT4

4.74e-0528523GO:0072207
GeneOntologyBiologicalProcessrenal system development

CFH OVOL1 WNT7B PDGFD WNT9B WNT4 SMAD2

4.93e-05386527GO:0072001
GeneOntologyBiologicalProcessmetanephros morphogenesis

WNT7B WNT9B WNT4

5.27e-0529523GO:0003338
GeneOntologyBiologicalProcessnephron development

CFH WNT7B PDGFD WNT9B WNT4

7.61e-05174525GO:0072006
GeneOntologyBiologicalProcessmetanephric tubule formation

WNT9B WNT4

9.29e-056522GO:0072174
GeneOntologyBiologicalProcesssmooth muscle cell differentiation

PROK2 CFH WNT7B WNT4

1.13e-0499524GO:0051145
GeneOntologyBiologicalProcessmetanephric tubule morphogenesis

WNT9B WNT4

2.77e-0410522GO:0072173
GeneOntologyCellularComponentcell surface

CFH VWF LPA WNT7B UNC5C BTLA TNFRSF11A WNT4 LY9 GRM7 VWDE TNFRSF4

1.68e-0511115312GO:0009986
GeneOntologyCellularComponentexternal side of plasma membrane

CFH VWF LPA BTLA TNFRSF11A LY9 TNFRSF4

3.20e-04519537GO:0009897
DomainSushi

CFH CFHR5 CSMD3 F13B CFHR3

3.23e-0752525PF00084
DomainCCP

CFH CFHR5 CSMD3 F13B CFHR3

3.92e-0754525SM00032
DomainSUSHI

CFH CFHR5 CSMD3 F13B CFHR3

4.71e-0756525PS50923
DomainSushi_SCR_CCP_dom

CFH CFHR5 CSMD3 F13B CFHR3

5.15e-0757525IPR000436
DomainVWD

VWF MUC5B VWDE

1.11e-0516523SM00216
DomainVWF_type-D

VWF MUC5B VWDE

1.11e-0516523IPR001846
DomainVWFD

VWF MUC5B VWDE

1.11e-0516523PS51233
DomainVWD

VWF MUC5B VWDE

1.11e-0516523PF00094
DomainCTCK_1

CCN6 VWF MUC5B

1.61e-0518523PS01185
DomainWnt

WNT7B WNT9B WNT4

1.91e-0519523IPR005817
DomainWnt_CS

WNT7B WNT9B WNT4

1.91e-0519523IPR018161
Domainwnt

WNT7B WNT9B WNT4

1.91e-0519523PF00110
DomainWNT1

WNT7B WNT9B WNT4

1.91e-0519523SM00097
DomainWNT1

WNT7B WNT9B WNT4

1.91e-0519523PS00246
DomainCT

CCN6 VWF MUC5B

3.02e-0522523SM00041
DomainCys_knot_C

CCN6 VWF MUC5B

4.48e-0525523IPR006207
DomainCTCK_2

CCN6 VWF MUC5B

4.48e-0525523PS01225
DomainCUB

PDGFD TMPRSS7 CSMD3

3.43e-0449523PF00431
DomainCUB

PDGFD TMPRSS7 CSMD3

3.64e-0450523SM00042
Domain-

PDGFD TMPRSS7 CSMD3

4.09e-04525232.60.120.290
Domainzf-RING_2

PJA2 PJA1 RFWD3

4.09e-0452523PF13639
DomainCUB

PDGFD TMPRSS7 CSMD3

4.32e-0453523PS01180
DomainTIL

VWF MUC5B

4.93e-0412522PF01826
DomainC8

VWF MUC5B

4.93e-0412522PF08742
DomainCUB_dom

PDGFD TMPRSS7 CSMD3

5.36e-0457523IPR000859
DomainUnchr_dom_Cys-rich

VWF MUC5B

5.82e-0413522IPR014853
DomainC8

VWF MUC5B

5.82e-0413522SM00832
DomainTIL_dom

VWF MUC5B

6.77e-0414522IPR002919
DomainTSP_1

CCN6 UNC5C ADAMTS17

7.18e-0463523PF00090
DomainGlyco_hormone_CN

CCN6 MUC5B

7.80e-0415522IPR006208
DomainCys_knot

CCN6 MUC5B

7.80e-0415522PF00007
DomainTSP1

CCN6 UNC5C ADAMTS17

7.87e-0465523SM00209
DomainTSP1_rpt

CCN6 UNC5C ADAMTS17

7.87e-0465523IPR000884
DomainTSP1

CCN6 UNC5C ADAMTS17

7.87e-0465523PS50092
DomainIG

IGSF22 TRIO UNC5C BTLA IGSF1 LY9

1.07e-03421526SM00409
DomainIg_sub

IGSF22 TRIO UNC5C BTLA IGSF1 LY9

1.07e-03421526IPR003599
DomainVWC_out

VWF MUC5B

1.26e-0319522SM00215
DomainZnf_C3HC4_RING-type

PJA2 PJA1 RFWD3 RBCK1

1.33e-03172524IPR018957
DomainRING

PJA2 ZMYND11 PJA1 RFWD3 RBCK1

1.56e-03305525SM00184
Domainzf-RanBP

NEIL3 RBCK1

1.69e-0322522PF00641
DomainTNFR_c6

TNFRSF11A TNFRSF4

1.69e-0322522PF00020
DomainZnF_RBZ

NEIL3 RBCK1

1.85e-0323522SM00547
DomainZF_RANBP2_2

NEIL3 RBCK1

1.85e-0323522PS50199
DomainZF_RANBP2_1

NEIL3 RBCK1

2.02e-0324522PS01358
DomainZnf_RING

PJA2 ZMYND11 PJA1 RFWD3 RBCK1

2.09e-03326525IPR001841
DomainZnf_RanBP2

NEIL3 RBCK1

2.19e-0325522IPR001876
DomainIG_LIKE

IGSF22 TRIO UNC5C BTLA IGSF1 LY9

2.34e-03491526PS50835
DomainTNFR

TNFRSF11A TNFRSF4

2.37e-0326522SM00208
DomainIg-like_dom

IGSF22 TRIO UNC5C BTLA IGSF1 LY9

2.64e-03503526IPR007110
DomainVWC

VWF MUC5B

2.74e-0328522PF00093
DomainTNFR_NGFR_1

TNFRSF11A TNFRSF4

2.94e-0329522PS00652
DomainTNFR_NGFR_2

TNFRSF11A TNFRSF4

2.94e-0329522PS50050
DomainEGF_LAM_2

LAMA2 STAB1

3.15e-0330522PS50027
DomainEGF_LAM_1

LAMA2 STAB1

3.15e-0330522PS01248
Domainzf-C3HC4

PJA2 PJA1 RFWD3 RBCK1

3.42e-03223524PF00097
DomainTNFR/NGFR_Cys_rich_reg

TNFRSF11A TNFRSF4

3.80e-0333522IPR001368
DomainIGc2

IGSF22 TRIO UNC5C IGSF1

4.12e-03235524SM00408
DomainIg_sub2

IGSF22 TRIO UNC5C IGSF1

4.12e-03235524IPR003598
DomainLaminin_EGF

LAMA2 STAB1

4.27e-0335522PF00053
DomainEGF_Lam

LAMA2 STAB1

4.27e-0335522SM00180
DomainVWFC_1

VWF MUC5B

4.51e-0336522PS01208
DomainVWC

VWF MUC5B

5.01e-0338522SM00214
DomainVWFC_2

VWF MUC5B

5.01e-0338522PS50184
DomainLaminin_EGF

LAMA2 STAB1

5.01e-0338522IPR002049
DomainVWF_dom

VWF MUC5B

6.10e-0342522IPR001007
Domain-

PJA2 ZMYND11 PJA1 RFWD3 RBCK1

8.07e-034495253.30.40.10
PathwayKEGG_MEDICUS_REFERENCE_REGULATION_OF_COMPLEMENT_CASCADE_CFHR

CFH CFHR5 CFHR3

3.89e-076393M47880
PathwayKEGG_MEDICUS_REFERENCE_WNT_SIGNALING_MODULATION_WNT_ACYLATION

WNT7B WNT9B WNT4

1.84e-0519393M47836
PathwayWP_BLOOD_CLOTTING_CASCADE

VWF LPA F13B

3.34e-0523393MM15936
PathwayREACTOME_WNT_LIGAND_BIOGENESIS_AND_TRAFFICKING

WNT7B WNT9B WNT4

4.32e-0525393MM14940
PathwayREACTOME_WNT_LIGAND_BIOGENESIS_AND_TRAFFICKING

WNT7B WNT9B WNT4

4.87e-0526393M27239
PathwayKEGG_MEDICUS_REFERENCE_WNT_SIGNALING_MODULATION_WNT_INHIBITOR

WNT7B WNT9B WNT4

6.11e-0528393M47835
PathwayKEGG_MEDICUS_VARIANT_MUTATION_INACTIVATED_PTCH1_TO_HEDGEHOG_SIGNALING_PATHWAY

WNT7B WNT9B WNT4

6.81e-0529393M47372
PathwayKEGG_MEDICUS_VARIANT_MUTATION_ACTIVATED_SMO_TO_HEDGEHOG_SIGNALING_PATHWAY

WNT7B WNT9B WNT4

6.81e-0529393M47377
PathwayWP_WNT_SIGNALING_IN_KIDNEY_DISEASE

WNT7B WNT9B WNT4

1.31e-0436393M39699
PathwayKEGG_MEDICUS_VARIANT_FZD7_OVEREXPRESSION_TO_WNT_SIGNALING_PATHWAY

WNT7B WNT9B WNT4

1.43e-0437393M47411
PathwayWP_WNT_SIGNALING_IN_KIDNEY_DISEASE

WNT7B WNT9B WNT4

2.40e-0444393MM15878
PathwayKEGG_MEDICUS_VARIANT_LRP6_OVEREXPRESSION_TO_WNT_SIGNALING_PATHWAY

WNT7B WNT9B WNT4

2.56e-0445393M47412
PathwayKEGG_MEDICUS_REFERENCE_WNT_SIGNALING_PATHWAY

WNT7B WNT9B WNT4

2.74e-0446393M47409
PathwayKEGG_BASAL_CELL_CARCINOMA

WNT7B WNT9B WNT4

4.65e-0455393M17807
PathwayKEGG_HEDGEHOG_SIGNALING_PATHWAY

WNT7B WNT9B WNT4

4.90e-0456393M1053
PathwayWP_COMPLEMENT_AND_COAGULATION_CASCADES

CFH VWF F13B

5.44e-0458393M39649
PathwayREACTOME_NEPHRON_DEVELOPMENT

WNT9B WNT4

5.71e-0413392M48245
PathwayWP_DENGUE2_INTERACTIONS_WITH_COMPLEMENT_AND_COAGULATION_CASCADES

CFH VWF F13B

5.72e-0459393M48343
PathwayKEGG_WNT_SIGNALING_PATHWAY

WNT7B WNT9B WNT4 SMAD2

7.77e-04151394M19428
PathwayPID_SMAD2_3PATHWAY

NUP214 SMAD2

8.73e-0416392M228
PathwayKEGG_COMPLEMENT_AND_COAGULATION_CASCADES

CFH VWF F13B

9.04e-0469393M16894
PathwayWP_EPITHELIAL_TO_MESENCHYMAL_TRANSITION_IN_COLORECTAL_CANCER

WNT7B WNT9B WNT4 SMAD2

9.87e-04161394M39770
PathwayWP_NEPHROGENESIS

WNT9B WNT4

1.11e-0318392M40045
PathwayREACTOME_GPCR_LIGAND_BINDING

PROK2 WNT7B WNT9B WNT4 GRM7 ECE2

1.58e-03463396M507
PathwayWP_POLYCYSTIC_KIDNEY_DISEASE_PATHWAY

WNT7B WNT9B WNT4

1.65e-0385393M48315
PathwayWP_BLOOD_CLOTTING_CASCADE

VWF F13B

1.66e-0322392M39480
PathwayKEGG_PATHWAYS_IN_CANCER

WNT7B WNT9B LAMA2 WNT4 SMAD2

1.91e-03325395M12868
PathwayREACTOME_CLASS_B_2_SECRETIN_FAMILY_RECEPTORS

WNT7B WNT9B WNT4

2.21e-0394393M797
Pubmed

Sequence and Expression of Complement Factor H Gene Cluster Variants and Their Roles in Age-Related Macular Degeneration Risk.

CFH CFHR5 CFHR3

7.46e-08655327196323
Pubmed

The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.

CFH CFHR5 F13B

7.46e-08655318541031
Pubmed

Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: characterization, ethnic distribution and evolutionary implications.

CFH CFHR5 CFHR3

7.46e-08655317438673
Pubmed

Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation.

CCN6 WNT7B WNT9B WNT4

2.83e-073555419185060
Pubmed

Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome.

CFH CFHR5 CFHR3

3.12e-07955320059470
Pubmed

FHR-1 Binds to C-Reactive Protein and Enhances Rather than Inhibits Complement Activation.

CFH CFHR5 CFHR3

3.12e-07955328533443
Pubmed

Wnt signaling in heart valve development and osteogenic gene induction.

WNT7B WNT9B WNT4

3.12e-07955319961844
Pubmed

Molecular genetic studies of Wnt signaling in the mouse.

WNT7B WNT9B WNT4

2.07e-061655310585256
Pubmed

The Wnts.

WNT7B WNT9B WNT4

2.07e-06165539889131
Pubmed

c-Met and NF-κB-dependent overexpression of Wnt7a and -7b and Pax2 promotes cystogenesis in polycystic kidney disease.

WNT7B WNT9B WNT4

2.07e-061655322677559
Pubmed

The interaction between factor H and Von Willebrand factor.

CFH VWF

2.46e-06255223991205
Pubmed

Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease).

CFH CFHR5

2.46e-06255216299065
Pubmed

Human endothelin converting enzyme-2 (ECE2): characterization of mRNA species and chromosomal localization.

EEF1AKMT4-ECE2 ECE2

2.46e-06255211718899
Pubmed

Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease.

CFH CFHR3

2.46e-06255220694013
Pubmed

Complement Factor H-Related 3 Enhanced Inflammation and Complement Activation in Human RPE Cells.

CFH CFHR3

2.46e-06255234819935
Pubmed

Human complement factor H is a reductase for large soluble von Willebrand factor multimers--brief report.

CFH VWF

2.46e-06255224008159
Pubmed

A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic Syndrome.

CFH CFHR3

2.46e-06255226490391
Pubmed

The interaction between factor H and VWF increases factor H cofactor activity and regulates VWF prothrombotic status.

CFH VWF

2.46e-06255224014239
Pubmed

Wnt family proteins are secreted and associated with the cell surface.

WNT7B WNT9B WNT4

2.50e-06175538167409
Pubmed

Deletion of the prorenin receptor from the ureteric bud causes renal hypodysplasia.

WNT7B WNT9B WNT4

3.00e-061855323704941
Pubmed

GLI3 repressor controls nephron number via regulation of Wnt11 and Ret in ureteric tip cells.

WNT7B WNT9B WNT4

3.00e-061855319809516
Pubmed

Genome-wide association study identifies susceptibility loci for IgA nephropathy.

CFH CFHR5 CFHR3

3.56e-061955321399633
Pubmed

Coronary Artery Formation Is Driven by Localized Expression of R-spondin3.

WNT7B WNT9B WNT4

3.56e-061955328834739
Pubmed

Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system.

WNT7B WNT9B WNT4

3.56e-061955316054034
Pubmed

Characterization of Wnt gene expression in developing and postnatal hair follicles and identification of Wnt5a as a target of Sonic hedgehog in hair follicle morphogenesis.

WNT7B WNT9B WNT4

3.56e-061955311520664
Pubmed

The canonical Wnt signaling pathway is not involved in renal cyst development in the kidneys of inv mutant mice.

WNT7B WNT9B WNT4

4.19e-062055321248711
Pubmed

Increased expression of Wnt2 and SFRP4 in Tsk mouse skin: role of Wnt signaling in altered dermal fibrillin deposition and systemic sclerosis.

WNT7B WNT9B WNT4

4.88e-062155317943183
Pubmed

The WNT7b promoter is regulated by TTF-1, GATA6, and Foxa2 in lung epithelium.

WNT7B WNT9B WNT4

4.88e-062155311914369
Pubmed

Epithelial Wnt10a Is Essential for Tooth Root Furcation Morphogenesis.

WNT7B WNT9B WNT4

4.88e-062155331914354
Pubmed

Hedgehog-GLI signaling in Foxd1-positive stromal cells promotes murine nephrogenesis via TGFβ signaling.

WNT9B WNT4 SMAD2

4.88e-062155329945868
Pubmed

Histone deacetylase 1 and 2 regulate Wnt and p53 pathways in the ureteric bud epithelium.

WNT7B WNT9B WNT4

5.64e-062255325758227
Pubmed

Renal developmental defects resulting from in utero hypoxia are associated with suppression of ureteric β-catenin signaling.

WNT7B WNT9B WNT4

5.64e-062255325587709
Pubmed

Activation of beta-Catenin in mouse prostate causes HGPIN and continuous prostate growth after castration.

WNT7B WNT9B WNT4

5.64e-062255318991257
Pubmed

Does murine spermatogenesis require WNT signalling? A lesson from Gpr177 conditional knockout mouse models.

WNT7B WNT9B WNT4

6.48e-062355327362799
Pubmed

Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent.

CFH CFHR3

7.36e-06355220581873
Pubmed

Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome.

CFH CFHR3

7.36e-06355226163426
Pubmed

Complement factor H: sequence analysis of 221 kb of human genomic DNA containing the entire fH, fHR-1 and fHR-3 genes.

CFH CFHR3

7.36e-06355210781834
Pubmed

Association assessment of copy number polymorphism and risk of age-related macular degeneration.

CFH CFHR3

7.36e-06355221856016
Pubmed

Smad2 nucleocytoplasmic shuttling by nucleoporins CAN/Nup214 and Nup153 feeds TGFbeta signaling complexes in the cytoplasm and nucleus.

NUP214 SMAD2

7.36e-06355212191473
Pubmed

Proteoglycans are required for maintenance of Wnt-11 expression in the ureter tips.

WNT7B WNT4

7.36e-0635528951078
Pubmed

Variants in Complement Factor H and Complement Factor H-Related Protein Genes, CFHR3 and CFHR1, Affect Complement Activation in IgA Nephropathy.

CFH CFHR3

7.36e-06355225205734
Pubmed

Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency.

CFH CFHR3

7.36e-06355218006700
Pubmed

Atypical hemolytic uremic syndrome associated with complement factor H autoantibodies and CFHR1/CFHR3 deficiency.

CFH CFHR3

7.36e-06355219531976
Pubmed

PJA1, encoding a RING-H2 finger ubiquitin ligase, is a novel human X chromosome gene abundantly expressed in brain.

PJA2 PJA1

7.36e-06355212036302
Pubmed

Evaluation of CFH Y402H polymorphism and CFHR3/CFHR1 deletion in age-related macular degeneration patients from Brazil.

CFH CFHR3

7.36e-06355226942649
Pubmed

An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD).

CFH CFHR3

7.36e-06355220843825
Pubmed

Associations of CFH polymorphisms and CFHR1-CFHR3 deletion with blood pressure and hypertension in Chinese population.

CFH CFHR3

7.36e-06355222848687
Pubmed

A genome-wide association study identifies key modulators of complement factor H binding to malondialdehyde-epitopes.

CFH CFHR3

7.36e-06355232321835
Pubmed

Two factor H-related proteins from the mouse: expression analysis and functional characterization.

CFH CFHR3

7.36e-06355217028856
Pubmed

Localization of complement factor H gene expression and protein distribution in the mouse outer retina.

CFH CFHR3

7.36e-06355225684976
Pubmed

A Wnt7b-dependent pathway regulates the orientation of epithelial cell division and establishes the cortico-medullary axis of the mammalian kidney.

WNT7B WNT9B WNT4

9.48e-062655319060336
Pubmed

Activation of the Wnt-beta catenin pathway in a cell population on the surface of the forebrain is essential for the establishment of olfactory axon connections.

WNT7B WNT9B WNT4

1.07e-052755317804636
Pubmed

Frizzled 1 and frizzled 2 genes function in palate, ventricular septum and neural tube closure: general implications for tissue fusion processes.

WNT7B WNT9B WNT4

1.19e-052855320940229
Pubmed

Ectodermal Wnt signaling regulates abdominal myogenesis during ventral body wall development.

WNT7B WNT9B WNT4

1.19e-052855324394376
Pubmed

Wnt5a potentiates TGF-β signaling to promote colonic crypt regeneration after tissue injury.

WNT7B WNT9B WNT4

1.33e-052955322956684
Pubmed

3D representation of Wnt and Frizzled gene expression patterns in the mouse embryo at embryonic day 11.5 (Ts19).

WNT7B WNT9B WNT4

1.33e-052955318364260
Pubmed

Atypical haemolytic-uraemic syndrome due to heterozygous mutations of CFH/CFHR1-3 and complement factor H 479.

CFH CFHR3

1.47e-05455224333077
Pubmed

Genetic susceptibility to chronic otitis media with effusion: candidate gene single nucleotide polymorphisms.

MUC5B SMAD2

1.47e-05455223929584
Pubmed

Canonical WNT signaling during kidney development.

WNT7B WNT4

1.47e-05455217494089
Pubmed

Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci.

CFH CFHR5

1.47e-05455234563268
Pubmed

Six2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney development.

WNT9B WNT4

1.47e-05455218682239
Pubmed

CFH and CFHR structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome.

CFH CFHR3

1.47e-05455236793547
Pubmed

Mutational analysis of the WNT gene family in women with Mayer-Rokitansky-Kuster-Hauser syndrome.

WNT9B WNT4

1.47e-05455219171330
Pubmed

Genetic interactions of the androgen and Wnt/beta-catenin pathways for the masculinization of external genitalia.

WNT7B WNT9B WNT4

1.47e-053055319282366
Pubmed

Atlas of Wnt and R-spondin gene expression in the developing male mouse lower urogenital tract.

WNT7B WNT9B WNT4

1.47e-053055321936019
Pubmed

Expression of all Wnt genes and their secreted antagonists during mouse blastocyst and postimplantation development.

WNT7B WNT9B WNT4

1.47e-053055315880404
Pubmed

Overactive Wnt5a signaling disrupts hair follicle polarity during mouse skin development.

WNT7B WNT9B WNT4

1.47e-053055336305473
Pubmed

The non-canonical BMP and Wnt/β-catenin signaling pathways orchestrate early tooth development.

WNT7B WNT4 SMAD2

1.80e-053255325428587
Pubmed

Early embryonic expression of murine coagulation system components.

VWF LPA F13B

2.16e-053455311154109
Pubmed

WNT5A is transported via lipoprotein particles in the cerebrospinal fluid to regulate hindbrain morphogenesis.

WNT7B WNT9B WNT4

2.36e-053555330940800
Pubmed

GLI2 Modulated by SUFU and SPOP Induces Intestinal Stem Cell Niche Signals in Development and Tumorigenesis.

WNT7B WNT9B WNT4

2.36e-053555331167144
Pubmed

Tracing the origin of hair follicle stem cells.

WNT7B ADAMTS17 WNT4

2.36e-053555334108685
Pubmed

Complement factor H and related proteins: an expanding family of complement-regulatory proteins?

CFH CFHR3

2.45e-0555528172644
Pubmed

Factor H-related proteins determine complement-activating surfaces.

CFHR5 CFHR3

2.45e-05555225979655
Pubmed

Identification and sequence analysis of four complement factor H-related transcripts in mouse liver.

CFH CFHR3

2.45e-0555521689298
Pubmed

Increased IGF-1 in muscle modulates the phenotype of severe SMA mice.

TNFRSF11A GRM7

2.45e-05555221325354
Pubmed

Distinct domain utilization by Smad3 and Smad4 for nucleoporin interaction and nuclear import.

NUP214 SMAD2

2.45e-05555212917407
Pubmed

Molecular cloning of the b subunit of mouse coagulation factor XIII and assignment of the gene to chromosome 1: close evolutionary relationship to complement factor H.

CFH F13B

2.45e-0555528468048
Pubmed

Molecular basis of C-reactive protein binding and modulation of complement activation by factor H-related protein 4.

CFH CFHR3

2.45e-05555220042240
Pubmed

A radiation hybrid map of complement factor H and factor H-related genes.

CFH CFHR3

2.45e-05555210380701
Pubmed

Integrated analysis of Wnt signalling system component gene expression.

WNT7B WNT9B WNT4

2.80e-053755335831952
Pubmed

Wnt11 promotes cardiomyocyte development by caspase-mediated suppression of canonical Wnt signals.

WNT7B WNT9B WNT4

3.04e-053855321041481
Pubmed

Tissue-specific requirements of beta-catenin in external genitalia development.

WNT7B WNT9B WNT4

3.04e-053855318635608
Pubmed

Epidermal Wnt controls hair follicle induction by orchestrating dynamic signaling crosstalk between the epidermis and dermis.

WNT7B WNT9B WNT4

3.04e-053855323190887
Pubmed

Distinct requirements for cranial ectoderm and mesenchyme-derived wnts in specification and differentiation of osteoblast and dermal progenitors.

WNT7B WNT9B WNT4

3.28e-053955324586192
Pubmed

A RING finger protein Praja1 regulates Dlx5-dependent transcription through its ubiquitin ligase activity for the Dlx/Msx-interacting MAGE/Necdin family protein, Dlxin-1.

PJA2 PJA1

3.67e-05655211959851
Pubmed

Anterior-posterior guidance of commissural axons by Wnt-frizzled signaling.

WNT7B WNT4

3.67e-05655214671310
Pubmed

Differential regulation of the Wnt gene family during pregnancy and lactation suggests a role in postnatal development of the mammary gland.

WNT7B WNT4

3.67e-0565521373817
Pubmed

Dimerization of complement factor H-related proteins modulates complement activation in vivo.

CFH CFHR5

3.67e-05655223487775
Pubmed

Differential expression of human Wnt genes 2, 3, 4, and 7B in human breast cell lines and normal and disease states of human breast tissue.

WNT7B WNT4

3.67e-0565528168088
Pubmed

Identification of molecular determinants required for interaction of ubiquitin-conjugating enzymes and RING finger proteins.

UBE2L6 RBCK1

3.67e-05655211722579
Pubmed

Wnt/beta-catenin signaling regulates nephron induction during mouse kidney development.

WNT9B WNT4

3.67e-05655217537789
Pubmed

Growth of geographic atrophy on fundus autofluorescence and polymorphisms of CFH, CFB, C3, FHR1-3, and ARMS2 in age-related macular degeneration.

CFH CFHR3

3.67e-05655224557084
Pubmed

Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement.

CFH CFHR5

3.67e-05655223235567
Pubmed

Plasmin-mediated fibrinolysis enables macrophage migration in a murine model of inflammation.

LPA F13B

3.67e-05655231101623
Pubmed

Notch pathway activation can replace the requirement for Wnt4 and Wnt9b in mesenchymal-to-epithelial transition of nephron stem cells.

WNT9B WNT4

3.67e-05655221852398
Pubmed

A comprehensive framework of E2-RING E3 interactions of the human ubiquitin-proteasome system.

PJA2 UBE2L6 PJA1 RFWD3

3.76e-0511855419690564
Pubmed

Gpr177 regulates pulmonary vasculature development.

WNT7B WNT9B WNT4

4.73e-054455323884445
Pubmed

Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.

CFH CFHR5

5.13e-05755220513133
Pubmed

Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome.

CFH CFHR3

5.13e-05755219861685
CytobandEnsembl 112 genes in cytogenetic band chr1q31

CFH CFHR5 F13B CFHR3

2.10e-0675554chr1q31
Cytoband18q22.1

TNFRSF11A DSEL

2.13e-041855218q22.1
Cytoband3q13.2

BTLA TMPRSS7

6.41e-04315523q13.2
Cytoband1q32

CFH CFHR3

1.60e-03495521q32
GeneFamilyHyalectan proteoglycans|V-set domain containing|Sushi domain containing|C-type lectin domain containing

CFH CFHR5 CSMD3 F13B CFHR3

2.57e-07574451179
GeneFamilyWnt family|Endogenous ligands

WNT7B WNT9B WNT4

1.27e-0519443360
GeneFamilyComplement system|Sushi domain containing

CFH CFHR5 CFHR3

9.08e-0536443492
GeneFamilyZinc fingers RANBP2-type |RNA binding motif containing

NEIL3 RBCK1

1.18e-032144289
GeneFamilyCD molecules|Tumor necrosis factor receptor superfamily|Death inducing signaling complex

TNFRSF11A TNFRSF4

2.25e-0329442782
GeneFamilyEndogenous ligands

PROK2 VWF WNT7B WNT4

2.59e-03237444542
GeneFamilyRing finger proteins

PJA2 PJA1 RFWD3 RBCK1

4.41e-0327544458
GeneFamilyBlood group antigens|CD molecules|I-set domain containing|Immunoglobulin like domain containing

IGSF22 TRIO UNC5C

7.03e-03161443593
GeneFamilyImmunoglobulin like domain containing

BTLA IGSF1 LY9

1.15e-02193443594
GeneFamilyADAM metallopeptidase domain containing|CD molecules

BTLA TNFRSF11A LY9 TNFRSF4

1.52e-02394444471
CoexpressionNABA_MATRISOME

CCN6 VWF LPA WNT7B PDGFD WNT9B ADAMTS17 LAMA2 MUC5B WNT4 VWDE F13B

9.34e-0710085512MM17056
CoexpressionNABA_MATRISOME

CCN6 VWF LPA WNT7B PDGFD WNT9B ADAMTS17 LAMA2 MUC5B WNT4 VWDE F13B

1.12e-0610265512M5889
CoexpressionVART_KSHV_INFECTION_ANGIOGENIC_MARKERS_DN

PROK2 CFH WNT7B STAB1 CFHR3

9.52e-06135555M5825
CoexpressionVALK_AML_CLUSTER_3

CFH PDGFD TNFRSF4

5.00e-0534553M9858
CoexpressionGSE25123_CTRL_VS_ROSIGLITAZONE_STIM_PPARG_KO_MACROPHAGE_DN

CFH OVOL1 MUC5B LY9 PLEKHB1

6.13e-05199555M7998
CoexpressionGSE43955_1H_VS_60H_ACT_CD4_TCELL_WITH_TGFB_IL6_UP

CFH VWF LAMA2 PJA1 TNFRSF4

6.28e-05200555M9682
CoexpressionMIKKELSEN_NPC_HCP_WITH_H3K27ME3

PROK2 OVOL1 WNT9B TNFRSF11A WNT4 GRM7

8.38e-05345556M2009
CoexpressionMIKKELSEN_NPC_HCP_WITH_H3K27ME3

PROK2 OVOL1 WNT9B TNFRSF11A WNT4 GRM7

8.65e-05347556MM860
ToppCellParenchymal-NucSeq-Stromal-Chondrocytic|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

PROK2 OVOL1 UNC5C NEIL3 CSMD3 CFHR3

1.40e-07193556df4afb4848eb9d7d8d39e5c612919663cbbb2514
ToppCellParenchymal-NucSeq-Stromal-Chondrocytic-Chondrocyte|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

PROK2 OVOL1 UNC5C NEIL3 CSMD3 CFHR3

1.40e-07193556ab36d684bde8fe77d11a5188425135328052c58b
ToppCellrenal_medulla_nuclei-Hypertensive_with+without-CKD-Epithelial-Renal_corpuscle_epithelial_cell-parietal_epithelial_cell-Parietal_Epithelial_Cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

CFH EEF1AKMT4-ECE2 UNC5C NEIL3 GRM7

1.42e-06156555dd41ed918b07fa248da458a629b3c53cb7ea8764
ToppCellrenal_medulla_nuclei-Hypertensive_with+without-CKD-Epithelial-Renal_corpuscle_epithelial_cell-parietal_epithelial_cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

CFH EEF1AKMT4-ECE2 UNC5C NEIL3 GRM7

1.42e-06156555abf9dd075b1ca8f613c660cc82f8a5af071fb6ab
ToppCellAdult-Immune-dendritic_cell-D175|Adult / Lineage, Cell type, age group and donor

CDCA7 ZNF366 BTLA TNFRSF11A ZXDA

2.57e-061765551f0f1f953e6d61119f342de0d980aa1287511dba
ToppCellPCW_05-06-Endothelial-Endothelial_mature-endo_arterial_(9)|PCW_05-06 / Celltypes from embryonic and fetal-stage human lung

CFH VWF PLEKHB1 TNFRSF4 STAB1

2.87e-061805555861b44acfb8fe92c281c8355bf19c059b3dcd64
ToppCelllymphoid-NK_cell-TNFRSF18+IL7R+_NK_cell|World / Lineage, cell class and subclass

CCNJL CFH PDGFD UNC5C TNFRSF4

2.95e-061815550d096d7d557fd2e71b35e41816e11d7e83cd9210
ToppCelllymphoid-NK_cell-TNFRSF18+IL7R+_NK_cell|lymphoid / Lineage, cell class and subclass

CCNJL CFH PDGFD UNC5C TNFRSF4

3.46e-0618755599dfa50f6325b0d66d23ee8dcaa6437e7161628a
ToppCellPrimary_Motor_Cortex_(M1)-Neuronal-Inh_GABAergic-i_Gaba_2-GABA_VIP_2|Primary_Motor_Cortex_(M1) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

WNT4 DSEL GRM7 VWDE ECE2

3.55e-06188555c66fccdfe68760b8c3efca77e3c25966dc9a8a5f
ToppCellRV-01._Fibroblast_I|World / Chamber and Cluster_Paper

CFH PDGFD UNC5C ADAMTS17 LAMA2

3.83e-0619155570c067c54084bfb02c29bab085f4defd477194fb
ToppCellRV-01._Fibroblast_I|RV / Chamber and Cluster_Paper

CFH PDGFD UNC5C ADAMTS17 LAMA2

3.93e-06192555356160b113c3305a61ceeaff33ce3c9da0be2878
ToppCellCOVID-19-Heart-Fib_+_EC_+_Pericyte|Heart / Disease (COVID-19 only), tissue and cell type

CFH VWF PDGFD UNC5C LAMA2

3.93e-0619255560b1312e84f6d6448365a952469c506c00b5fe93
ToppCell5'-GW_trimst-2-LargeIntestine-Mesenchymal-fibroblastic-Stromal_1_(ADAMDEC1+)|GW_trimst-2 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

CFH PDGFD UNC5C PJA1 CSMD3

4.45e-06197555236a40eb6c08e1d179cf0fb5450b032975c5f6b6
ToppCelldistal-1-mesenchymal-Myofibroblast|1 / Location, Lineage, Cell class (ontology) and Donor from 10X sequencing (macrophage renamed)

CFH UNC5C LAMA2 IGSF1 GRM7

4.68e-0619955558c36f5a30c6862b7f5587a0b9bc31da99e43dd5
ToppCelldistal-mesenchymal-Myofibroblast-1|distal / Location, Lineage, Cell class (ontology) and Donor from 10X sequencing (macrophage renamed)

CFH UNC5C LAMA2 IGSF1 GRM7

4.68e-0619955579917b5225cb45b4a0ea937f79f1752346e4346e
ToppCellfrontal_cortex-Neuronal-GABAergic_neuron-Pvalb-Pvalb_Vipr2|frontal_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype

CDCA7 PDGFD ADAMTS17 TAFA2

2.71e-0514055472c272f44e5600b3037c1dbf9d3a4669a35588d8
ToppCellprimary_visual_cortex-Neuronal-glutamatergic_neuron-L5_IT-L5_IT_VISp_Whrn_Tox2|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype

WNT7B WNT4 TMPRSS7 TAFA2

2.94e-0514355436ce6f163fb33141c86288086c354b91853fad25
ToppCellrenal_cortex_nuclei-Hypertensive_with+without-CKD-Endothelial-blood_vessel_endothelial_cell_of_kidney-capillary-immature_endothelial_cell-Cycling_Endothelial_Cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

ZNF366 NEIL3 RFWD3 TNFRSF4

4.03e-05155554969fc4c98a96bf2f436e8e63d4deb2183ef3b864
ToppCellPND03-Immune-Immune_Myeloid-DC-maDC|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

UBE2L6 ZNF366 TNFRSF11A TNFRSF4

4.13e-05156554095281ea78aefa0ee638191a03f8d6f62a86a9ff
ToppCellPND03-Immune-Immune_Myeloid-DC-maDC-maDC_mature|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

UBE2L6 ZNF366 TNFRSF11A TNFRSF4

4.13e-0515655429b04143f71a0ecc600ac670abd1d521bee55fe7
ToppCelldroplet-Thymus-nan-18m-Myeloid-B_cell|Thymus / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

UBE2L6 MUC5B WNT4 SLC26A6

4.24e-05157554a9e077f686382303f0437ebfa4f11d273ba9fe40
ToppCellrenal_cortex_nuclei-CKD+DKD_normotensive-Endothelial-blood_vessel_endothelial_cell_of_kidney-arteriolar_vasa-recta_endothelial|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

VWF ZNF366 PDGFD TMPRSS7

5.14e-05165554a74751e0ec857aa974bec04ccc747c004a8f6e01
ToppCellTCGA-Liver-Primary_Tumor-Hepatocellular_Carcinoma-Hepatocellular_Carcinoma-8|TCGA-Liver / Sample_Type by Project: Shred V9

CFH VWF F13B CFHR3

5.91e-05171554c4a919fe3d56ae6df2fcab6686abacc10befc053
ToppCell3'-Broncho-tracheal-Mesenchymal-Fibroblastic-fibroblastic_type_1-Adventitial_fibroblasts-|3' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

CFH TRIO UNC5C LAMA2

6.04e-05172554e37c0b5b547a7345179ab258dd2141fec7064c17
ToppCellprimary_auditory_cortex_(A1C)|World / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

PROK2 PDGFD ECE2 ZNF541

6.04e-0517255420ea9db009370aa6235365ce93e153eb5b28db94
ToppCellP15-Mesenchymal-developing_mesenchymal_cell-mesenchymal_immature_unknown_1|P15 / developmental_time, Lineage, Cell group, Cell type, Cell type_cellcyc-phase

CFH ADAMTS17 IGSF1 TMPRSS7

6.32e-051745543c47d069bd836599a8d40eae485c23d4d3487517
ToppCellPND14-Immune-Immune_Myeloid-DC-cDC1-cDC1_prolif|PND14 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

CFH NEIL3 BTLA DSEL

6.32e-0517455409b091e24317c3f7bac043f04762a533e30793de
ToppCell10x5'-blood-Lymphocytic_Invariant-Inducer-like|blood / Manually curated celltypes from each tissue

CFH OVOL1 WNT4 DNAH7

6.32e-0517455451be6f29308c01593978cbee92114151a5916c9c
ToppCellTCGA-Liver|World / Sample_Type by Project: Shred V9

LPA CFHR5 F13B CFHR3

6.32e-05174554452932f08cf53e5949672a025d78cecb874aa4b0
ToppCellTCGA-Colorectal-Recurrent_Tumor|TCGA-Colorectal / Sample_Type by Project: Shred V9

LPA CFHR5 F13B CFHR3

6.46e-051755547f74961436f88c0e380819095e6104489914d765
ToppCellrenal_medulla_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Fibroblast-kidney_interstitial_fibroblast-Adaptive_/_Maladaptive_/_Repairing_Fibroblast|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

CFH UNC5C LAMA2 ADGRG4

6.46e-05175554795a6564d5a75ffd35d39f5274b9e8d28708bbc8
ToppCellTCGA-Colorectal-Recurrent_Tumor-Colorectal_Adenocarcinoma|TCGA-Colorectal / Sample_Type by Project: Shred V9

LPA CFHR5 F13B CFHR3

6.46e-05175554bee8f31f036dfcf9fc6ed29156554771a9ee3c60
ToppCell10x5'-blood-Lymphocytic_Invariant-Inducer-like-MAIT|blood / Manually curated celltypes from each tissue

CFH OVOL1 WNT4 DNAH7

6.46e-05175554b4e4b66e89f79999768a6192c8404cb2465f920b
ToppCellrenal_papilla_nuclei-Adult_normal_reference-Mesenchymal-Fibroblast-kidney_interstitial_fibroblast-Adaptive_/_Maladaptive_/_Repairing_Fibroblast|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

CFH ADAMTS17 LAMA2 GRM7

6.75e-051775549ec7f1e64312d26d434b3312b58386715dbad644
ToppCellrenal_papilla_nuclei-Adult_normal_reference-Mesenchymal-Fibroblast-kidney_interstitial_fibroblast|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

CFH ADAMTS17 LAMA2 GRM7

6.75e-05177554016277dfd59b1793fddaaadc2b3f41622d76ce3a
ToppCellAnterior_Cingulate_gyrus_(CgG)-Neuronal-Glutamatergic_Excit-Glut_C-D_(RORB)-Glut_D_(IT_RORB_THEMIS_LINC00507)_2|Anterior_Cingulate_gyrus_(CgG) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

LAMA2 GRM7 DNAH7 TAFA2

6.90e-051785540e1bedf991189d0ef9b40dac9281bdf4739333a1
ToppCellwk_15-18-Endothelial-Blood_vessel_endothelial-OMD+_endo|wk_15-18 / Celltypes from embryonic and fetal-stage human lung

CFH VWF PDGFD ZNF541

7.05e-051795548c9ed247e1c4d655b81ce2f24a9936a7cade718a
ToppCellEpithelial-basal_cell|World / Lineage, Cell type, age group and donor

CFH LPA WNT4 VWDE

7.05e-05179554d9be6647ec7b22747dc00dce4ea307b6af412dfa
ToppCellRA-01._Fibroblast_I|World / Chamber and Cluster_Paper

CFH UNC5C LAMA2 CFHR3

7.36e-051815542b6ddeb53a79a658e2ba78527ff48c155b20daa6
ToppCell5'-GW_trimst-1-SmallIntestine-Endothelial-blood_vessel_EC-Fetal_arterial_EC|GW_trimst-1 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

VWF ZNF366 BTLA TNFRSF4

7.36e-051815547d7d1edeae4e0ebe40b324d1231cd26e27ba9d42
ToppCell5'-GW_trimst-1.5-LargeIntestine-Endothelial-blood_vessel_EC-venous_capillary|GW_trimst-1.5 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

VWF ZNF366 TNFRSF4 STAB1

7.52e-0518255463b41b538b26bc899558807fd035e543611f8c52
ToppCellwk_15-18-Hematologic_Lymphocytic-T_&_ILC-ILCP|wk_15-18 / Celltypes from embryonic and fetal-stage human lung

TNFRSF11A LY9 GRM7 TNFRSF4

7.52e-051825546bd48c5d60a259719f65cacee4b8135247e78fa9
ToppCellCOVID-19-Heart-Fib_+_EC_+_Pericyte|COVID-19 / Disease (COVID-19 only), tissue and cell type

VWF PDGFD UNC5C LAMA2

7.52e-05182554fbd5e332df73bf7141c822fa67b76367dc962017
ToppCellrenal_medulla_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Fibroblast-kidney_interstitial_fibroblast|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

CFH UNC5C LAMA2 ADGRG4

7.85e-05184554e061e85c4bb19f49f6451ddd7a9077d7378ee365
ToppCellSomatosensory_Cortex_(S1)-Neuronal-Glutamatergic_Excit-Glut_C-D_(RORB)-Glut_C_(IT_L4_RORB)|Somatosensory_Cortex_(S1) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

LAMA2 GRM7 DNAH7 TAFA2

7.85e-051845546475a43201b136dcc9b113d2ca4cfa154ed9d65d
ToppCellfacs-Heart-LA-18m-Endothelial-endocardial_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CFH VWF ADAMTS17 STAB1

8.01e-051855541ecfca049c0c1110fd1b2256db7cb7abda6afb04
ToppCellfacs-Heart-LA-18m-Endothelial-endothelial_cell_of_endocardium|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CFH VWF ADAMTS17 STAB1

8.01e-05185554b6df1412b579d40ed5df806f9c54bd1fbb9a1e15
ToppCelldroplet-Bladder-BLADDER-1m-Hematologic-nan|Bladder / Skin_Bladder_Kidney_Mammary_Gland - method, tissue, subtissue, age, lineage, cell ontology and free annotation

VWF CDCA7 NEIL3 LY9

8.01e-05185554969248b63d4ce335f223528de756bcddffadbd77
ToppCellfacs-Trachea-3m-Epithelial-airway_epithelial|3m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype

OVOL1 WNT7B MUC5B WNT4

8.18e-0518655437b93ebd64ebbd08193a746e5bc9b350c2570733
ToppCelldroplet-Kidney-KIDNEY-1m-Mesenchymal-fibroblast|Kidney / Skin_Bladder_Kidney_Mammary_Gland - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CFH ADAMTS17 LAMA2 GRM7

8.18e-0518655494d577dbb6bfacf50632e1fe8af041b35a1e6b23
ToppCellfacs-Trachea-3m-Epithelial-airway_epithelial-respiratory_basal_cell|3m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype

OVOL1 WNT7B MUC5B WNT4

8.52e-051885548ffb5394f7b00ea483a5fe4df894d22fda935e5c
ToppCellCOVID-19-Heart-Fib_1|COVID-19 / Disease (COVID-19 only), tissue and cell type

CFH PDGFD UNC5C LAMA2

8.52e-05188554fe361215f4ba841aa5e1e581fb56f2f4d3ccd201
ToppCellControl-Fibroblasts-Adventitial_FB|Control / group, cell type (main and fine annotations)

CFH PDGFD UNC5C LAMA2

8.52e-05188554706a26c372add839d947749f0521a0e1f5c9b0ec
ToppCell5'-Adult-LargeIntestine-Mesenchymal-fibroblastic-Stromal_2_(NPY+)|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract

CFH PDGFD WNT4 CFHR3

8.52e-05188554997dcfc4f08738ab398d8abc15e4fd2fc6619862
ToppCellfacs-Trachea-3m-Epithelial-airway_epithelial-respiratory_basal_cell-basal_epithelial_cell_of_trachea|3m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype

OVOL1 WNT7B MUC5B WNT4

8.52e-05188554137ed9958044fab7a13648affb469585d1c48cf6
ToppCelldroplet-Heart-nan-3m-Endothelial-endocardial_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CCNJL CFH VWF STAB1

8.70e-051895548e583ec4df0f5b79ce5211cc99ecd8616d180bde
ToppCellrenal_medulla_nuclei-Hypertensive_with+without-CKD-Endothelial-blood_vessel_endothelial_cell_of_kidney-arteriolar_vasa-recta_endothelial-Descending_Vasa_Recta_Endothelial_Cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

CFH VWF ZNF366 PDGFD

8.70e-051895546463890d8dbee4bc198f91628a5f784970de786a
ToppCelldroplet-Heart-nan-3m-Endothelial-endocardial_endothelial_cells|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CCNJL CFH VWF STAB1

8.70e-05189554fb2253b8463d08b3d28e952a31a23dea2c2d986b
ToppCellCOVID-19-kidney-AQP1+SLC14A1+EC|kidney / Disease (COVID-19 only), tissue and cell type

CFH VWF ZNF366 PDGFD

8.88e-051905541519f34d31fe0817184c5865a0bc9f0cb479b1a4
ToppCellfacs-Trachea-18m-Epithelial-airway_epithelial|18m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype

OVOL1 WNT7B MUC5B WNT4

9.06e-05191554cd4e2e883c4955fb2d875e41bb6ebc680994dc8c
ToppCellrenal_cortex_nuclei-Adult_normal_reference-Mesenchymal-Fibroblast-kidney_interstitial_fibroblast-Adaptive_/_Maladaptive_/_Repairing_Fibroblast|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

CFH PDGFD LAMA2 ADGRG4

9.06e-051915542c51850f5c559d665b8a27a12b75af9ed58dffe1
ToppCellnucseq-Mesenchymal-Fibroblastic-Fibroblastic_2-AF1|nucseq / Celltype signatures by Technology, Lineage, Lineage_subclass, Celltype_group, Cell_type2

CFH UNC5C ADAMTS17 LAMA2

9.06e-051915546688cee34beee4f151ac17fccbc9c26a9aad72e1
ToppCelldroplet-Heart-nan-18m-Endothelial-endocardial_endothelial_cells|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CFH VWF ADAMTS17 STAB1

9.25e-051925540b9b2eaed45456d7d74ce78a64ef4a26ac2458fb
ToppCell3'-Child04-06-SmallIntestine-Epithelial-Tuft-related|Child04-06 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

LPA TNFRSF11A PLEKHB1 ADGRG4

9.25e-05192554d6ea34391c3f730684b82e912d9cf55e928b3311
ToppCell10x5'-lymph-node_spleen-Lymphocytic_Invariant-Inducer-like-ILC3|lymph-node_spleen / Manually curated celltypes from each tissue

UNC5C TNFRSF11A GRM7 TNFRSF4

9.25e-05192554e16035b3328f9b1b2e28d234c62ba88387540550
ToppCellnucseq-Mesenchymal-Fibroblastic-Fibroblastic_2|nucseq / Celltype signatures by Technology, Lineage, Lineage_subclass, Celltype_group, Cell_type2

CFH UNC5C ADAMTS17 LAMA2

9.25e-0519255499ce9e3c4c50cf64ebb62145f2b5420efa0db309
ToppCellfacs-Trachea-18m-Epithelial|18m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype

OVOL1 WNT7B MUC5B WNT4

9.25e-05192554c5823c5d4c58a4e9121a4b7d7256481d6d9e9b7f
ToppCellAdult-Mesenchymal-matrix_fibroblast_2_cell|Adult / Lineage, Cell type, age group and donor

CFH UNC5C LAMA2 ADGRG4

9.25e-05192554d21f0f577156f17c899b08871046a26b88aea011
ToppCellTracheal-NucSeq-Stromal-Peri/Epineurial_-NAF_endoneurial|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

CFH PDGFD LAMA2 CSMD3

9.43e-05193554549a0b750c860b615aff767ad04c9a9d20f802f0
ToppCell5'-Adult-SmallIntestine-Mesenchymal-fibroblastic-mLN_Stroma_(FMO2+)|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract

CFH UNC5C LAMA2 IGSF1

9.43e-051935547c0d84b92470bfda2db1e5007feee7c1235a0a78
ToppCellSmart-start-Cell-Wel_seq-Non-neoplastic-Lymphoid-CD4/CD8-Reg_T-E|Smart-start-Cell-Wel_seq / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group

BTLA LY9 VWDE TNFRSF4

9.43e-051935547deb439943d35a4e825674b2b7dcddb45d366ad1
ToppCellLV-01._Fibroblast_I|LV / Chamber and Cluster_Paper

CFH PDGFD UNC5C LAMA2

9.43e-05193554dc17f3b9758936d428cf17f77a1ce6d4c479b165
ToppCellRV-02._Fibroblast_II|RV / Chamber and Cluster_Paper

CFH PDGFD UNC5C LAMA2

9.62e-0519455411c79a8c56ece42713b04b321982e41e239f07a5
ToppCelldroplet-Heart-4Chambers-21m-Endothelial-endocardial_endothelial_cells|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CCNJL CFH VWF STAB1

9.62e-05194554c5e77650d7abee339ec38fa78a622bb124db3fa5
ToppCellLV-02._Fibroblast_II|LV / Chamber and Cluster_Paper

CFH PDGFD UNC5C LAMA2

9.62e-05194554014d2feb5db2a6a35ef759761a41e466e108c3c1
ToppCellCOVID-19-Heart-Fib_2|Heart / Disease (COVID-19 only), tissue and cell type

CFH PDGFD UNC5C LAMA2

9.62e-05194554d91c9f2ec47319051fc398320693fddbe8bbd4d6
ToppCell10x_3'_v2v3-Neoplastic-Differentiated-like-AC-like-AC-like-E|10x_3'_v2v3 / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group

PJA2 TRIO LAMA2 DSEL

9.62e-051945548b81f039f5b25d35a4d5a41b27d4d9360ba22f15
ToppCellLA-02._Fibroblast_II|LA / Chamber and Cluster_Paper

CFH PDGFD UNC5C LAMA2

9.62e-05194554234d1494c114cce77c619708bbcd8d5ce805f19b
ToppCellPCW_05-06-Endothelial-Endothelial_mature|PCW_05-06 / Celltypes from embryonic and fetal-stage human lung

CFH VWF TNFRSF4 STAB1

9.82e-0519555454fde2cfa51ab3a2d48d2426494ca6f0ce77f725
ToppCellCOVID-19-Heart-Fib_1|Heart / Disease (COVID-19 only), tissue and cell type

CFH PDGFD UNC5C LAMA2

9.82e-05195554f423baa36ac7cdc383c033e35a7d17e6bf913323
ToppCelldroplet-Heart-4Chambers-21m-Endothelial-endocardial_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CCNJL CFH VWF STAB1

9.82e-05195554df644b4c3ddccd34614ece5a2378000e6bc0fa10
ToppCell3'-GW_trimst-1-LargeIntestine-Endothelial-blood_vessel_EC-venous_capillary|GW_trimst-1 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

VWF ZNF366 TNFRSF4 STAB1

9.82e-05195554ccfb80e3bfdf5304fa798e0a47b473955ecc0c6d
ToppCellRV-02._Fibroblast_II|World / Chamber and Cluster_Paper

CFH PDGFD UNC5C LAMA2

9.82e-05195554ce90b30dcdb56d4cd925cdb79fd9d7cefd998f48
ToppCellRA-02._Fibroblast_II|RA / Chamber and Cluster_Paper

CFH PDGFD UNC5C LAMA2

9.82e-051955546a02ebbeb3199447ddce64d92d8809436e040eba
ToppCellTracheal-10x5prime-Immune_Lymphocytic-B-B_plasma-B_plasma_IgA|10x5prime / Cell types per location group and 10X technology with lineage, and cell group designations

NEIL3 BTLA LY9 TNFRSF4

9.82e-05195554df009b18898c10686f75cf72b4ec0eff18f5bb50
ToppCelldroplet-Heart-HEART_(ALL_MINUS_AORTA)-30m-Endothelial-endocardial_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CFH VWF WNT4 STAB1

1.00e-041965547d5eaed189aa6116f3799be010139fb675ec65e0
ToppCell3'-GW_trimst-2-LargeIntestine-Mesenchymal-fibroblastic-Stromal_1_(ADAMDEC1+)|GW_trimst-2 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

CFH PJA1 DSEL CSMD3

1.00e-04196554a7adc0e0baef261d0937e4e8351321d41beca82f
ToppCellHealthy-CD4+_CTL|Healthy / disease group, cell group and cell class

PROK2 CFH LY9 DSEL

1.00e-041965549da0ea4ad84d6e20e4349d3d1a8cc4d61d08c84f
ToppCelldroplet-Heart-nan-18m-Endothelial-endocardial_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CFH VWF ADAMTS17 STAB1

1.00e-04196554e386526332138e636aef2542c11316347a45689c
ToppCellBronchial-10x5prime-Immune_Lymphocytic-NK-ILC-T_NK-ILC|10x5prime / Cell types per location group and 10X technology with lineage, and cell group designations

CDCA7 ADAMTS17 CSMD3 TNFRSF4

1.00e-041965541cc2b11764584129703ec61965e8ec4e051464e7
ToppCell3'-Adult-LymphNode-Endothelial-lymphatic_endothelial-LEC1_(ACKR4+)|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract

VWF PDGFD TNFRSF4 STAB1

1.00e-04196554aa52f77f80c3fe23369347a34e0b3188b768a763
ToppCelldroplet-Heart-HEART_(ALL_MINUS_AORTA)-30m-Endothelial-endocardial_endothelial_cells|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CFH VWF WNT4 STAB1

1.00e-04196554dbf154b3d166ffd07be717dac8d8a3350ac63e16
ToppCellnucseq-Mesenchymal-Fibroblastic|nucseq / Celltype signatures by Technology, Lineage, Lineage_subclass, Celltype_group, Cell_type2

CFH UNC5C ADAMTS17 LAMA2

1.00e-041965547d8505dac15fa59935ccf592afc54b04c4c6554f
ToppCellBronchial-10x5prime-Epithelial-Epi_airway_basal-Dividing_Basal|10x5prime / Cell types per location group and 10X technology with lineage, and cell group designations

OVOL1 CDCA7 NEIL3 WNT4

1.02e-0419755425bbe270d0897b9b1bd00d205f66efd1def81b99
ToppCelldistal-mesenchymal-Myofibroblast-2|distal / Location, Lineage, Cell class (ontology) and Donor from 10X sequencing (macrophage renamed)

CFH LAMA2 GRM7 CFHR3

1.04e-04198554beef5075ba6dcd4d0a447bc4e57efcaf2e93c546
ToppCellLPS_only-Epithelial_airway-airway_epithelial|LPS_only / Treatment groups by lineage, cell group, cell type

OVOL1 WNT7B MUC5B DNAH7

1.04e-04198554e035380578c01b0243bfef29ca9b50cc17cce771
ToppCellLPS_only-Epithelial_airway|LPS_only / Treatment groups by lineage, cell group, cell type

OVOL1 WNT7B MUC5B DNAH7

1.04e-04198554ba090210392e001a3f7bdf09371b3f0e0c8c7ef3
ToppCellPosterior_cortex-Neuronal-Inhibitory-iN2(Gad1Gad2)-Synpr-Inhibitory_Neuron.Gad1Gad2-Chat.Synpr-Slc5a7_(Neuron.Gad1Gad2-Chat.Synpr-Slc5a7)|Posterior_cortex / BrainAtlas - Mouse McCarroll V32

PROK2 CCN6 F13B

1.05e-04745530d705c42e7741b861ba5a9f1af83b2c5c6f23fb6
ToppCellPosterior_cortex-Neuronal-Inhibitory-iN2(Gad1Gad2)-Synpr-Inhibitory_Neuron.Gad1Gad2-Chat.Synpr-Slc5a7_(Neuron.Gad1Gad2-Chat.Synpr-Slc5a7)-|Posterior_cortex / BrainAtlas - Mouse McCarroll V32

PROK2 CCN6 F13B

1.05e-0474553c49bda52aa4ead9483c2f27d63458034e75699bd
ToppCellControl_saline-Epithelial_airway-airway_epithelial-Airway-Club|Control_saline / Treatment groups by lineage, cell group, cell type

OVOL1 WNT7B MUC5B IGSF1

1.06e-041995545cc8b553a58669a30eb10845beb23983dcdf5a6a
DrugFactor Xiiib

CFH LPA CFHR5 F13B

1.30e-0635534CID000126166
Drug(2S)-N-[4-(aminomethyl)-1,1-dioxothian-4-yl]-2-[1-(benzenesulfonamido)ethylideneamino]-3-(1-methylcyclopentyl)propanamide

CFH CFHR3

5.32e-062532CID011840931
Diseasecoagulation factor measurement

CFH VWF CFHR5

6.46e-0620543EFO_0004634
Diseaseendoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase measurement

CFH CFHR3

9.85e-063542EFO_0801568
Diseasecomplement C5 measurement

CFHR5 F13B

9.85e-063542EFO_0020278
Diseaseanaphase-promoting complex subunit 7 measurement

CFH CFHR3

9.85e-063542EFO_0801381
DiseaseHEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1

CFH CFHR3

9.85e-063542C2749604
DiseaseHEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1

CFH CFHR3

9.85e-063542235400
DiseaseHemolytic uremic syndrome, atypical, susceptibility to, 1

CFH CFHR3

9.85e-063542cv:C2749604
Diseaseplatelet-derived growth factor receptor alpha measurement

CFHR5 F13B

9.85e-063542EFO_0021844
DiseaseNADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial measurement

CFH CFHR3

1.97e-054542EFO_0803292
DiseaseMeningococcal Infections

CFH CFHR3

1.97e-054542C0025303
DiseaseComplement deficiency disease

CFH CFHR5 CFHR3

3.04e-0533543C0272242
DiseaseDrug habituation

ZNF366 TMPRSS7 CSMD3 GRM7

5.96e-05115544C0013170
DiseaseDrug abuse

ZNF366 TMPRSS7 CSMD3 GRM7

5.96e-05115544C0013146
DiseasePrescription Drug Abuse

ZNF366 TMPRSS7 CSMD3 GRM7

5.96e-05115544C4316881
DiseaseSubstance-Related Disorders

ZNF366 TMPRSS7 CSMD3 GRM7

5.96e-05115544C0236969
DiseaseDrug Use Disorders

ZNF366 TMPRSS7 CSMD3 GRM7

5.96e-05115544C0013222
DiseaseDrug Dependence

ZNF366 TMPRSS7 CSMD3 GRM7

5.96e-05115544C1510472
DiseaseSubstance Dependence

ZNF366 TMPRSS7 CSMD3 GRM7

5.96e-05115544C0038580
DiseaseSubstance Use Disorders

ZNF366 TMPRSS7 CSMD3 GRM7

5.96e-05115544C0038586
DiseaseOrganic Mental Disorders, Substance-Induced

ZNF366 TMPRSS7 CSMD3 GRM7

5.96e-05115544C0029231
DiseaseSubstance abuse problem

ZNF366 TMPRSS7 CSMD3 GRM7

6.16e-05116544C0740858
Diseasecomplement factor H-related protein 5 measurement

CFH CFHR5 F13B

6.32e-0542543EFO_0008098
Diseasemesangial proliferative glomerulonephritis (biomarker_via_orthology)

VWF PDGFD

9.14e-058542DOID:4783 (biomarker_via_orthology)
Diseaseatypical hemolytic-uremic syndrome (is_implicated_in)

CFH CFHR3

9.14e-058542DOID:0080301 (is_implicated_in)
DiseaseC3 glomerulopathy

CFH CFHR5

1.17e-049542C4087273
DiseaseAtypical hemolytic-uremic syndrome

CFH CFHR3

1.17e-049542cv:C2931788
DiseaseHemolytic-uremic syndrome

CFH CFHR3

1.17e-049542cv:C0019061
DiseaseAtypical Hemolytic Uremic Syndrome

CFH CFHR3

1.47e-0410542C2931788
Diseasecomplement factor H-related protein 1 measurement

CFH CFHR5 F13B

1.50e-0456543EFO_0600054
Diseasehemopexin measurement

CFH CFHR5

1.79e-0411542EFO_0008149
Diseasemethylcobalamin deficiency type cblE, brain serotonin transporter measurement

VWF TRIO

3.88e-0416542EFO_0004569, MONDO_0009354
DiseaseSLAM family member 7 measurement

CFH LY9

4.39e-0417542EFO_0008287
DiseaseAge-related macular degeneration

CFH CFHR3

4.94e-0418542cv:C0242383
Diseasebrain age measurement

EEF1AKMT4-ECE2 ECE2

6.12e-0420542EFO_0010602
DiseaseDeep Vein Thrombosis

LPA F13B

6.75e-0421542C0149871
DiseaseVenous Thrombosis

LPA F13B

6.75e-0421542C0042487
DiseaseL lactate dehydrogenase measurement

CFH STAB1

1.04e-0326542EFO_0004808
Diseasepancreatic ductal adenocarcinoma (is_marker_for)

SMAD2 CFHR3

1.12e-0327542DOID:3498 (is_marker_for)
Diseasefactor VIII measurement, von Willebrand factor measurement

VWF ZNF366

1.12e-0327542EFO_0004629, EFO_0004630
Diseasecomplement factor H-related protein 2 measurement

CFH F13B

1.29e-0329542EFO_0600055
DiseaseAge related macular degeneration

CFH CFHR3

1.38e-0330542C0242383
Diseaseunipolar depression

CFH TRIO WNT7B UNC5C MUC5B CSMD3 GRM7 DNAH7

1.49e-031206548EFO_0003761
Diseaseangina pectoris

CFH LPA UNC5C

1.57e-03125543EFO_0003913
Diseasefrontotemporal dementia

PJA2 VWDE

1.57e-0332542MONDO_0017276

Protein segments in the cluster

PeptideGeneStartEntry
VCLWKGCKVYNTPST

AEBP2

296

Q6ZN18
WSDHRPVCKVKTCGS

CSMD3

536

Q7Z407
RPHVTWCKLNGTTCV

BTLA

66

Q7Z6A9
CSISINTGKSQWEKP

ADGRG4

2426

Q8IZF6
TWPTTCPRKTKECLK

CCNJL

216

Q8IV13
WSPTPRCIRVKTCSK

CFH

436

P08603
SQCSASCGKGVWKRT

ADAMTS17

931

Q8TE56
SCGKGVWKRTVACTN

ADAMTS17

936

Q8TE56
VWKRTVACTNSQGKC

ADAMTS17

941

Q8TE56
TTSQGTTRCQPKCEW

MUC5B

1776

Q9HC84
ISTWLKGQVRKCPQC

RFWD3

316

Q6PCD5
SVSAKIPETKWCQKC

MAP4K3

661

Q8IVH8
WTCVVCTLINKPSSK

NEIL3

321

Q8TAT5
TVCHTEICWVTKGPR

RBCK1

466

Q9BYM8
KKSCVPRWQTCISNT

ECE2

466

P0DPD6
GWSLTPKCTKLKCSS

F13B

201

P05160
VNWRSCTCNSGKTVK

PDGFD

311

Q9GZP0
STVAVTSVCWSPKGK

NUP214

191

P35658
TIGEKCSKCAPNTWG

LAMA2

1036

P24043
LVKKPCVSTCKRNWS

OVOL1

6

O14753
CAVSIWVKSIRICTP

PROK2

46

Q9HC23
VQATKWTPCSRTCGM

CCN6

211

O95389
GTKKSCVPRWQTCIS

EEF1AKMT4-ECE2

536

P0DPD8
PKAQTTVTCTEKGWS

CFHR3

121

Q02985
WSKCTKIPISGTCYT

IGSF22

846

Q8N9C0
KNLTLWCRSPSGSTK

IGSF1

606

Q8N6C5
KEWTTLCKGRDIPCS

DNAH7

2931

Q8WXX0
KKATTVTGTPCQEWA

LPA

1731

P08519
WTTLPTCVEQVKTCG

CFHR5

256

Q9BXR6
WKRKGRCSVPAFCSS

LY9

476

Q9HBG7
QRKKTQKGTPCCWTC

GRM7

531

Q14831
STCSQPICAKWTRTE

DSEL

821

Q8IZU8
ECKVLPDRKGWSCSS

TAFA2

106

Q8N3H0
CWKLPQSKVGTVVTA

SLC26A6

256

Q9BXS9
KTIDTKTNCRNPDCW

CDCA7

276

Q9BWT1
GWSGKRCNTPICLQK

VWDE

1511

Q8N2E2
SGSCTTKTCWTTLPK

WNT7B

206

P56706
KVVTWRTATLCPQSC

VWF

1116

P04275
PPKCKCTWKFQTSLS

TMPRSS7

391

Q7RTY8
SKVRCVTRSWSPCKV

PLEKHB1

146

Q9UF11
NTKCVTIPSTCSEIW

SMAD2

71

Q15796
SSENWKPCTKTCQVL

UBE2L6

91

O14933
SPWSSCNKNVVGRCK

TTMP

51

Q5BVD1
SCAAIKKQTCPSGWL

STAB1

46

Q9NY15
CKPWTNCTLAGKHTL

TNFRSF4

141

P43489
WKSRCPISSCNKLFT

ZXDA

541

P98168
SSSPWQCPVCRSIKK

ZMYND11

136

Q15326
VGGSQKRWQCPTCEK

ZNF366

246

Q8N895
VSGSCEVKTCWRAVP

WNT4

211

P56705
WKVICKSCISQTPGI

XAGE1A

36

Q9HD64
SGSCAVRTCWKQLSP

WNT9B

216

O14905
CVSIWLQKSGTCPVC

PJA1

621

Q8NG27
KIACTTLCPVDGRWT

UNC5C

306

O95185
VSIWLQKSGTCPVCR

PJA2

661

O43164
VISCWKGVCVPQTTT

TMEM78

11

Q5T7P6
CRVCGRPKASITWKG

TRIO

2706

O75962
TDKCRPWTNCTFLGK

TNFRSF11A

166

Q9Y6Q6
WTKPRSTFVCKNCSQ

ZNF541

831

Q9H0D2