Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyCellularComponentactin-based cell projection

PCDH15 MPP1 ABI1 MYO7A ABI2

2.03e-04278415GO:0098858
GeneOntologyCellularComponentpostsynaptic density

SRGAP2 CLSTN2 ABI1 DST DRP2 KALRN

2.31e-04451416GO:0014069
GeneOntologyCellularComponentSCAR complex

ABI1 ABI2

2.45e-0412412GO:0031209
GeneOntologyCellularComponentasymmetric synapse

SRGAP2 CLSTN2 ABI1 DST DRP2 KALRN

3.12e-04477416GO:0032279
GeneOntologyCellularComponentstereocilium

PCDH15 MPP1 MYO7A

3.35e-0469413GO:0032420
GeneOntologyCellularComponentpostsynaptic specialization

SRGAP2 CLSTN2 ABI1 DST DRP2 KALRN

4.14e-04503416GO:0099572
GeneOntologyCellularComponentstereocilium bundle

PCDH15 MPP1 MYO7A

4.99e-0479413GO:0032421
GeneOntologyCellularComponentneuron to neuron synapse

SRGAP2 CLSTN2 ABI1 DST DRP2 KALRN

5.09e-04523416GO:0098984
GeneOntologyCellularComponentfilopodium tip

ABI1 ABI2

6.97e-0420412GO:0032433
GeneOntologyCellularComponentpostsynapse

SRGAP2 CLSTN2 ABI1 DST DRP2 KALRN ABI2 SRGAP3

7.00e-041018418GO:0098794
GeneOntologyCellularComponentglutamatergic synapse

SRGAP2 CLSTN2 ABI1 DRP2 KALRN ABI2 SRGAP3

9.56e-04817417GO:0098978
GeneOntologyCellularComponentchromosomal region

CDT1 ATM TNKS2 CENPC SUN2

1.33e-03421415GO:0098687
GeneOntologyCellularComponentcondensed chromosome

CDT1 CENPC POLB SUN2

3.01e-03307414GO:0000793
MousePhenoenlarged stomach

ANKRD20A3P ANKRD20A8P ANKRD20A4P ANKRD20A1

1.44e-0633364MP:0003883
DomainSH3

MPP1 SRGAP2 ABI1 DST KALRN MYO7A ABI2 SRGAP3 SRGAP1

1.56e-09216449PS50002
DomainSH3_domain

MPP1 SRGAP2 ABI1 DST KALRN MYO7A ABI2 SRGAP3 SRGAP1

1.84e-09220449IPR001452
DomainSH3

MPP1 SRGAP2 ABI1 KALRN MYO7A ABI2 SRGAP3 SRGAP1

3.48e-08216448SM00326
DomainSH3_1

SRGAP2 ABI1 DST ABI2 SRGAP3 SRGAP1

2.24e-06164446PF00018
DomainAbl-interactor_HHR_dom

ABI1 ABI2

1.62e-053442IPR012849
DomainAbi_HHR

ABI1 ABI2

1.62e-053442PF07815
DomainFCH

SRGAP2 SRGAP3 SRGAP1

1.82e-0522443PF00611
DomainFCH

SRGAP2 SRGAP3 SRGAP1

1.82e-0522443SM00055
DomainSpectrin

DST DRP2 KALRN

2.09e-0523443PF00435
DomainFCH_dom

SRGAP2 SRGAP3 SRGAP1

2.09e-0523443IPR001060
DomainF_BAR

SRGAP2 SRGAP3 SRGAP1

2.71e-0525443IPR031160
DomainF_BAR

SRGAP2 SRGAP3 SRGAP1

2.71e-0525443PS51741
DomainSpectrin_repeat

DST DRP2 KALRN

4.27e-0529443IPR002017
DomainSpectrin/alpha-actinin

DST DRP2 KALRN

5.77e-0532443IPR018159
DomainSPEC

DST DRP2 KALRN

5.77e-0532443SM00150
DomainAnk_2

ANKRD20A2P ANKRD20A3P TNKS2 ANKRD20A4P ANKRD20A1

1.45e-04215445PF12796
DomainAnk

ANKRD20A2P ANKRD20A3P TNKS2 ANKRD20A4P ANKRD20A1

1.91e-04228445PF00023
Domain-

ANKRD20A2P ANKRD20A3P TNKS2 ANKRD20A4P ANKRD20A1

2.82e-042484451.25.40.20
DomainANK

ANKRD20A2P ANKRD20A3P TNKS2 ANKRD20A4P ANKRD20A1

2.98e-04251445SM00248
DomainANK_REPEAT

ANKRD20A2P ANKRD20A3P TNKS2 ANKRD20A4P ANKRD20A1

3.09e-04253445PS50088
DomainAnkyrin_rpt-contain_dom

ANKRD20A2P ANKRD20A3P TNKS2 ANKRD20A4P ANKRD20A1

3.15e-04254445IPR020683
DomainANK_REP_REGION

ANKRD20A2P ANKRD20A3P TNKS2 ANKRD20A4P ANKRD20A1

3.15e-04254445PS50297
DomainAnkyrin_rpt

ANKRD20A2P ANKRD20A3P TNKS2 ANKRD20A4P ANKRD20A1

3.63e-04262445IPR002110
DomainRhoGAP

SRGAP2 SRGAP3 SRGAP1

4.19e-0462443SM00324
DomainRhoGAP

SRGAP2 SRGAP3 SRGAP1

4.39e-0463443PF00620
DomainRHOGAP

SRGAP2 SRGAP3 SRGAP1

4.60e-0464443PS50238
DomainRhoGAP_dom

SRGAP2 SRGAP3 SRGAP1

4.60e-0464443IPR000198
Domain-

SRGAP2 SRGAP3 SRGAP1

4.60e-04644431.10.555.10
DomainRho_GTPase_activation_prot

SRGAP2 SRGAP3 SRGAP1

1.16e-0388443IPR008936
DomainT_SNARE

ABI1 ABI2

1.70e-0326442PS50192
DomainT_SNARE_dom

ABI1 ABI2

2.11e-0329442IPR000727
DomainKinase-like_dom

ATM STK40 DST KALRN PRKX

8.63e-03542445IPR011009
PathwayREACTOME_INACTIVATION_OF_CDC42_AND_RAC1

SRGAP2 SRGAP3 SRGAP1

6.49e-078333M27349
PathwayREACTOME_RAC1_GTPASE_CYCLE

SRGAP2 ABI1 KALRN ABI2 SRGAP3 SRGAP1

2.82e-06175336MM15599
PathwayREACTOME_RAC1_GTPASE_CYCLE

SRGAP2 ABI1 KALRN ABI2 SRGAP3 SRGAP1

3.77e-06184336M41809
PathwayREACTOME_RHO_GTPASE_CYCLE

SRGAP2 ABI1 DST KALRN ABI2 SRGAP3 SRGAP1

5.73e-05439337MM15595
PathwayREACTOME_RHO_GTPASE_CYCLE

SRGAP2 ABI1 DST KALRN ABI2 SRGAP3 SRGAP1

6.70e-05450337M27078
PathwayREACTOME_SIGNALING_BY_RHO_GTPASES_MIRO_GTPASES_AND_RHOBTB3

SRGAP2 ABI1 DST CENPC KALRN ABI2 SRGAP3 SRGAP1

9.64e-05649338MM15690
PathwayREACTOME_SIGNALING_BY_RHO_GTPASES_MIRO_GTPASES_AND_RHOBTB3

SRGAP2 ABI1 DST CENPC KALRN ABI2 SRGAP3 SRGAP1

1.98e-04720338M41838
PathwayREACTOME_SENSORY_PROCESSING_OF_SOUND_BY_OUTER_HAIR_CELLS_OF_THE_COCHLEA

PCDH15 MPP1 MYO7A

2.82e-0455333M41823
PathwayREACTOME_SENSORY_PROCESSING_OF_SOUND

PCDH15 MPP1 MYO7A

7.60e-0477333M41822
Pubmed

Expression of testicular germ cell genes identified by differential display analysis.

ANKRD20A3P ANKRD20A8P ANKRD20A4P ANKRD20A1

1.70e-10845412634303
Pubmed

Dynamic expression of the Slit-Robo GTPase activating protein genes during development of the murine nervous system.

SRGAP2 SRGAP3 SRGAP1

2.02e-09345319137586
Pubmed

SRGAP1 Controls Small Rho GTPases To Regulate Podocyte Foot Process Maintenance.

SRGAP2 SRGAP3 SRGAP1

4.04e-08645333514561
Pubmed

FNBP2 gene on human chromosome 1q32.1 encodes ARHGAP family protein with FCH, FBH, RhoGAP and SH3 domains.

SRGAP2 SRGAP3 SRGAP1

4.04e-08645312736724
Pubmed

Signal transduction in neuronal migration: roles of GTPase activating proteins and the small GTPase Cdc42 in the Slit-Robo pathway.

SRGAP2 SRGAP3 SRGAP1

4.04e-08645311672528
Pubmed

Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia.

SRGAP2 DST KALRN ABI2 SRGAP3 GOLGA4

4.29e-0815145617043677
Pubmed

Evidence for a role of srGAP3 in the positioning of commissural axons within the ventrolateral funiculus of the mouse spinal cord.

SRGAP2 SRGAP3 SRGAP1

7.06e-08745321655271
Pubmed

Identification of SH3 domain interaction partners of human FasL (CD178) by phage display screening.

SRGAP2 KALRN SRGAP3 SRGAP1

5.39e-075045419807924
Pubmed

Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I.

PCDH15 MYO7A

1.64e-06245222690115
Pubmed

Iron-inhibited autophagy via transcription factor ZFP27 in Parkinson's disease.

ZNF585A ZNF585B

1.64e-06245237668106
Pubmed

Role for the Abi/wave protein complex in T cell receptor-mediated proliferation and cytoskeletal remodeling.

ABI1 ABI2

1.64e-06245216401422
Pubmed

Identification of SRGAP2 as a potential oncogene and a prognostic biomarker in hepatocellular carcinoma.

SRGAP2 SRGAP1

1.64e-06245233984363
Pubmed

The Abl interactor proteins localize to sites of actin polymerization at the tips of lamellipodia and filopodia.

ABI1 ABI2

1.64e-06245211516653
Pubmed

Slit-Robo GTPase-activating proteins are differentially expressed in murine dorsal root ganglia: modulation by peripheral nerve injury.

SRGAP3 SRGAP1

1.64e-06245222271578
Pubmed

ATM regulates Cdt1 stability during the unperturbed S phase to prevent re-replication.

CDT1 ATM

1.64e-06245224280901
Pubmed

Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64.

MYO7A DIABLO

1.64e-06245221722859
Pubmed

The inverse F-BAR domain protein srGAP2 acts through srGAP3 to modulate neuronal differentiation and neurite outgrowth of mouse neuroblastoma cells.

SRGAP2 SRGAP3

1.64e-06245223505444
Pubmed

Regulation of cell-cell adhesion by Abi/Diaphanous complexes.

ABI1 ABI2

4.91e-06345219158278
Pubmed

Molecular screening of deafness in Algeria: high genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F.

PCDH15 MYO7A

4.91e-06345219375528
Pubmed

In search of a function for the E3B1/Abi2/Argbp1/NESH family (Review).

ABI1 ABI2

4.91e-06345212011975
Pubmed

Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%.

PCDH15 MYO7A

4.91e-06345216679490
Pubmed

Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis.

PCDH15 MYO7A

4.91e-06345227440999
Pubmed

Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells.

PCDH15 MYO7A

9.81e-06445216481439
Pubmed

Abl interactor 1 (Abi-1) wave-binding and SNARE domains regulate its nucleocytoplasmic shuttling, lamellipodium localization, and wave-1 levels.

ABI1 ABI2

9.81e-06445215143189
Pubmed

Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.

PCDH15 MYO7A

9.81e-06445218463160
Pubmed

Localization and phosphorylation of Abl-interactor proteins, Abi-1 and Abi-2, in the developing nervous system.

ABI1 ABI2

9.81e-06445210995551
Pubmed

Mechanotransduction is required for establishing and maintaining mature inner hair cells and regulating efferent innervation.

PCDH15 MYO7A

9.81e-06445230275467
Pubmed

Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice.

PCDH15 MYO7A

9.81e-06445221156003
Pubmed

Role of the F-box protein Skp2 in cell proliferation in the developing auditory system in mice.

SKP2 MYO7A

9.81e-06445212692478
Pubmed

Degradation of Cdt1 during S phase is Skp2-independent and is required for efficient progression of mammalian cells through S phase.

CDT1 SKP2

9.81e-06445215855168
Pubmed

A dual-activity topoisomerase complex regulates mRNA translation and turnover.

SRGAP2 ATG9A STK40 ZNF585A DST KALRN MYO7A PHF12 INTS11

1.01e-05110545935748872
Pubmed

Interactions in the network of Usher syndrome type 1 proteins.

PCDH15 MYO7A

1.63e-05545215590703
Pubmed

Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.

PCDH15 MYO7A

1.63e-05545215660226
Pubmed

ABI2-deficient mice exhibit defective cell migration, aberrant dendritic spine morphogenesis, and deficits in learning and memory.

ABI1 ABI2

1.63e-05545215572692
Pubmed

Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells.

PCDH15 MYO7A

1.63e-05545216219682
Pubmed

Abl-interactor-1 (Abi1) has a role in cardiovascular and placental development and is a binding partner of the alpha4 integrin.

ABI1 ABI2

1.63e-05545221173240
Pubmed

Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes.

PCDH15 MYO7A

1.63e-05545222381527
Pubmed

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.

PCDH15 MYO7A

1.63e-05545211398101
Pubmed

Impact of the Usher syndrome on olfaction.

PCDH15 MYO7A

2.45e-05645226620972
Pubmed

The SCF(Skp2) ubiquitin ligase complex interacts with the human replication licensing factor Cdt1 and regulates Cdt1 degradation.

CDT1 SKP2

2.45e-05645212840033
Pubmed

Cyclin-dependent kinases phosphorylate human Cdt1 and induce its degradation.

CDT1 SKP2

2.45e-05645215004027
Pubmed

The ORC ubiquitin ligase OBI1 promotes DNA replication origin firing.

CDT1 SKP2 NFIL3

2.58e-054445331160578
Pubmed

Fat3 acts through independent cytoskeletal effectors to coordinate asymmetric cell behaviors during polarized circuit assembly.

ABI1 ABI2

3.42e-05745235108541
Pubmed

JNK1 phosphorylation of Cdt1 inhibits recruitment of HBO1 histone acetylase and blocks replication licensing in response to stress.

CDT1 SKP2

3.42e-05745221856198
Pubmed

DNA repair gene polymorphisms and risk of pancreatic cancer.

ATM POLB

3.42e-05745219147782
Pubmed

Skp2 E3 ligase integrates ATM activation and homologous recombination repair by ubiquitinating NBS1.

ATM SKP2

3.42e-05745222464731
Pubmed

Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes.

PCDH15 MYO7A

3.42e-05745215572405
Pubmed

Usher Syndrome Type I

PCDH15 MYO7A

3.42e-05745220301442
Pubmed

Cdt1 phosphorylation by cyclin A-dependent kinases negatively regulates its function without affecting geminin binding.

CDT1 SKP2

3.42e-05745214993212
Pubmed

Specific and ubiquitous expression of different Zn finger protein genes in the mouse.

ZNF585A ZNF585B

3.42e-0574523143103
Pubmed

Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia.

PCDH15 MYO7A

3.42e-05745221436032
Pubmed

Microarray-based mutation analysis of 183 Spanish families with Usher syndrome.

PCDH15 MYO7A

4.56e-05845219683999
Pubmed

Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane.

PCDH15 MYO7A

4.56e-05845221165971
Pubmed

HIV-1 Vpr-induced apoptosis is cell cycle dependent and requires Bax but not ANT.

ATM DIABLO

4.56e-05845217140287
Pubmed

UMD-USHbases: a comprehensive set of databases to record and analyse pathogenic mutations and unclassified variants in seven Usher syndrome causing genes.

PCDH15 MYO7A

4.56e-05845218484607
Pubmed

Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.

PCDH15 MYO7A

4.56e-05845216545802
Pubmed

Structure and control of the actin regulatory WAVE complex.

ABI1 ABI2

4.56e-05845221107423
Pubmed

The histone demethylase LSD1/KDM1A promotes the DNA damage response.

CDT1 ATM

5.86e-05945224217620
Pubmed

Tonotopic gradient in the developmental acquisition of sensory transduction in outer hair cells of the mouse cochlea.

PCDH15 MYO7A

5.86e-05945219339464
Pubmed

A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth.

PCDH15 MYO7A

5.86e-05945218339676
Pubmed

Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1.

PCDH15 MYO7A

7.32e-051045224618850
Pubmed

Usher protein functions in hair cells and photoreceptors.

PCDH15 MYO7A

7.32e-051045224239741
Pubmed

NESH (Abi-3) is present in the Abi/WAVE complex but does not promote c-Abl-mediated phosphorylation.

ABI1 ABI2

7.32e-051045217101133
Pubmed

Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane.

PCDH15 MYO7A

8.94e-051145231776257
Pubmed

CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells.

PCDH15 MYO7A

1.07e-041245228663585
Pubmed

DDB1 is essential for genomic stability in developing epidermis.

CDT1 ATM

1.27e-041345217301228
Pubmed

Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.

PCDH15 MYO7A

1.47e-041445226754646
Pubmed

Parkin mediates the ubiquitination of VPS35 and modulates retromer-dependent endosomal sorting.

ATG9A GOLGA4

1.70e-041545229893854
Pubmed

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

SRGAP2 ABI1 DST KALRN ABI2 SRGAP3 GOLGA4

2.21e-0496345728671696
Pubmed

Gene Expression by Mouse Inner Ear Hair Cells during Development.

PCDH15 MYO7A

2.76e-041945225904789
Pubmed

Identification of novel human Cdt1-binding proteins by a proteomics approach: proteolytic regulation by APC/CCdh1.

CDT1 SKP2

3.06e-042045218162579
Pubmed

A quantitative survey of gravity receptor function in mutant mouse strains.

PCDH15 MYO7A

3.06e-042045216235133
Pubmed

The LIFEdb database in 2006.

ATG9A STK40 SUN2 ANKRD20A1 VCPIP1 INTS11

3.16e-0472045616381901
Pubmed

From ORFeome to biology: a functional genomics pipeline.

ATG9A STK40 SUN2 ANKRD20A1 VCPIP1 INTS11

3.21e-0472245615489336
Pubmed

Human Cytomegalovirus UL135 Interacts with Host Adaptor Proteins To Regulate Epidermal Growth Factor Receptor and Reactivation from Latency.

ABI1 ABI2

3.72e-042245230089695
Pubmed

Crosstalk between lysine methylation and phosphorylation of ATG16L1 dictates the apoptosis of hypoxia/reoxygenation-induced cardiomyocytes.

ATM TNKS2

3.72e-042245229634390
Pubmed

Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.

ATG9A STK40 SUN2 ANKRD20A1 VCPIP1 INTS11

3.92e-0475045611230166
Pubmed

A human skeletal muscle interactome centered on proteins involved in muscular dystrophies: LGMD interactome.

ABI1 DST TNKS2 KALRN NFIL3

4.45e-0449745523414517
Pubmed

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

TRAPPC10 SRGAP2 HTRA1 ABI1 DST KALRN MYO7A SRGAP3

4.46e-04143145837142655
Pubmed

Large-scale characterization of HeLa cell nuclear phosphoproteins.

TRAPPC10 CDT1 ATM PHF12 GOLGA4 VCPIP1

4.63e-0477445615302935
Pubmed

BioID reveals an ATG9A interaction with ATG13-ATG101 in the degradation of p62/SQSTM1-ubiquitin clusters.

TRAPPC10 ATG9A DST GOLGA4

5.05e-0428545434369648
Pubmed

HENA, heterogeneous network-based data set for Alzheimer's disease.

DST TNKS2 GOLGA4

5.11e-0412045331413325
Pubmed

Human origin recognition complex large subunit is degraded by ubiquitin-mediated proteolysis after initiation of DNA replication.

CDT1 SKP2

5.22e-042645211931757
Pubmed

PTEN dephosphorylates Abi1 to promote epithelial morphogenesis.

ABI1 ABI2

5.22e-042645232673396
Pubmed

DNA cloning using in vitro site-specific recombination.

ATG9A STK40 SUN2 ANKRD20A1 VCPIP1 INTS11

5.30e-0479445611076863
Pubmed

Atm deficiency in the DNA polymerase β null cerebellum results in cerebellar ataxia and Itpr1 reduction associated with alteration of cytosine methylation.

ATM POLB

6.50e-042945232123907
Pubmed

Proteomic analyses reveal distinct chromatin-associated and soluble transcription factor complexes.

ABI1 STK40 SKP2 ABI2 NFIL3 ANKRD20A1

7.90e-0485745625609649
Pubmed

A central chaperone-like role for 14-3-3 proteins in human cells.

SRGAP2 ABI1 DST SRGAP1 GOLGA4 VCPIP1

8.09e-0486145636931259
Pubmed

The addition of 5'-coding information to a 3'-directed cDNA library improves analysis of gene expression.

NFIL3 ADGRG6

1.06e-03374528076819
Pubmed

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

ODF2L SRGAP2 ATM DST TNKS2 KALRN VCPIP1

1.23e-03128545735914814
Pubmed

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

DST NFIL3 POLB PHF12 SUN2 VCPIP1 INTS11

1.28e-03129445730804502
InteractionANKRD20A4P interactions

ANKRD20A2P ANKRD20A4P ANKRD20A1

2.07e-076453int:ANKRD20A4P
InteractionANKRD20A2P interactions

ANKRD20A2P ANKRD20A4P ANKRD20A1

3.62e-077453int:ANKRD20A2P
InteractionDISC1 interactions

SRGAP2 ATG9A DST TNKS2 KALRN SKP2 ABI2 SRGAP3 SUN2

3.71e-07429459int:DISC1
InteractionANKRD20A1 interactions

ANKRD20A2P ANKRD20A4P ANKRD20A1

1.70e-0611453int:ANKRD20A1
InteractionRAPH1 interactions

ABI1 ABI2 SRGAP3 SRGAP1

1.25e-0564454int:RAPH1
InteractionPCDH15 interactions

PCDH15 MYO7A

7.27e-056452int:PCDH15
InteractionFASLG interactions

SRGAP2 KALRN SRGAP3 SRGAP1

8.80e-05105454int:FASLG
InteractionYWHAH interactions

TRAPPC10 SRGAP2 ABI1 ATG9A DST ABI2 DIABLO SRGAP1 GOLGA4 VCPIP1

1.27e-0411024510int:YWHAH
Cytoband9p12

ANKRD20A2P ANKRD20A3P

3.75e-04294529p12
GeneFamilyRho GTPase activating proteins|F-BAR domain containing

SRGAP2 SRGAP3 SRGAP1

7.90e-06233131288
GeneFamilyAnkyrin repeat domain containing

ANKRD20A2P ANKRD20A3P TNKS2 ANKRD20A4P ANKRD20A1

5.27e-05242315403
GeneFamilyRho GTPase activating proteins|BCH domain containing

SRGAP2 SRGAP3 SRGAP1

8.47e-0550313721
GeneFamilyCadherin related

PCDH15 CLSTN2

3.81e-041731224
GeneFamilyActins|Deafness associated genes

PCDH15 MYO7A DIABLO

9.41e-041133131152
ToppCellCOPD-Myeloid-cDC1|World / Disease state, Lineage and Cell class

ANKRD20A2P ANKRD20A3P ANKRD20A8P DST ANKRD20A4P ANKRD20A1

3.08e-0818445642d7ce104cd7bcb83fbbbd0e7d3267ad07edfa94
ToppCellCOPD-Myeloid-cDC1|Myeloid / Disease state, Lineage and Cell class

ANKRD20A2P ANKRD20A3P ANKRD20A8P ANKRD20A4P ANKRD20A1 ADGRG6

3.84e-081914563480e6d27dd4291765bbbb2acdb6a2e4f02c8085
ToppCell390C-Lymphocytic-NK_cells-NK_cell_C|Lymphocytic / Donor, Lineage, Cell class and subclass (all cells)

ANKRD20A2P ATM ANKRD20A4P KALRN ANKRD20A1

7.85e-0717045581341bf4fe090af70b2091b6b2579ed08d76e22d
ToppCellControl-Myeloid-cDC1|Myeloid / Disease state, Lineage and Cell class

ANKRD20A2P ANKRD20A3P ANKRD20A8P ANKRD20A4P ANKRD20A1

1.16e-06184455c6affa0b12510363258f65e46bf2d47bf4a8e75f
ToppCellrenal_cortex_nuclei-Hypertensive_with+without-CKD-Epithelial-Renal_corpuscle_epithelial_cell-glomerular_visceral_epithelial_cell-Podocyte|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 DST PRDM5 SRGAP1

1.19e-061854559197f074e769d54031ec41abfc65fcc0c6552c7e
ToppCellrenal_cortex_nuclei-Hypertensive_with+without-CKD-Epithelial-Renal_corpuscle_epithelial_cell-glomerular_visceral_epithelial_cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 DST PRDM5 SRGAP1

1.19e-06185455ce7d62394b09c26ca65b8cdb280afec5e25bbb62
ToppCellIPF-Myeloid-cDC1|World / Disease state, Lineage and Cell class

ANKRD20A2P ANKRD20A3P ANKRD20A8P ANKRD20A4P ANKRD20A1

1.22e-06186455962c2dada19185628ead77c32fcb07fa95114247
ToppCellControl-Myeloid-cDC1|Control / Disease state, Lineage and Cell class

ANKRD20A2P ANKRD20A3P ANKRD20A8P ANKRD20A4P ANKRD20A1

1.22e-06186455b05c394aa3573ba855abc3066739ca193883b0c3
ToppCell390C-Lymphocytic-NK_cells-NK_cell_C|390C / Donor, Lineage, Cell class and subclass (all cells)

ANKRD20A2P ATM ANKRD20A4P SUN2 ANKRD20A1

1.26e-061874551e8651e6c547384ace5a66b96c6b24a7f390a7ee
ToppCellIPF-Myeloid-cDC1|Myeloid / Disease state, Lineage and Cell class

ANKRD20A2P ANKRD20A3P ANKRD20A8P ANKRD20A4P ANKRD20A1

1.29e-0618845547bb6caf84f70a1cda7d09803afdfd5182772e66
ToppCellIPF-Myeloid-cDC1|IPF / Disease state, Lineage and Cell class

ANKRD20A2P ANKRD20A3P ANKRD20A8P ANKRD20A4P ANKRD20A1

1.29e-061884552331a2bae1383820d598e93aa86c75b101069bac
ToppCellCOPD-Myeloid-cDC1|COPD / Disease state, Lineage and Cell class

ANKRD20A2P ANKRD20A3P ANKRD20A8P ANKRD20A4P ANKRD20A1

1.43e-06192455bd3d00b094d92463b06023361a71240851a542b8
ToppCellmLN-(5)_Dendritic_cell-(53)_Lymphoid_DC|mLN / shred on region, Cell_type, and subtype

ANKRD20A2P ANKRD20A3P ANKRD20A4P SRGAP1 ANKRD20A1

1.66e-06198455da84c76afe835aeee39da04b63c03549218b5d91
ToppCellmLN-Dendritic_cell-Lymphoid_DC|mLN / Region, Cell class and subclass

ANKRD20A2P ANKRD20A3P ANKRD20A4P SRGAP1 ANKRD20A1

1.66e-061984553965a9f1e8a51a196e5349aaca5fa5ed1cd8ee92
ToppCellNeuronal-Inhibitory-iB-iB_4(SST)-STK32A|Neuronal / cells hierarchy compared to all cells using T-Statistic

PCDH15 HTRA1 PRKX SRGAP1 ADGRG6

1.75e-062004558d51b4f7b7002ee51401ebe5eaca1e8f04bfadd5
ToppCellNeuronal-Inhibitory-iB-iB_4(SST)-STK32A-|Neuronal / cells hierarchy compared to all cells using T-Statistic

PCDH15 HTRA1 PRKX SRGAP1 ADGRG6

1.75e-062004556a44439e4a7ce3627271375b04cfcfb9467218f4
ToppCellNeuronal-Inhibitory-iB-iB_4(SST)-STK32A--L4-5|Neuronal / cells hierarchy compared to all cells using T-Statistic

PCDH15 HTRA1 PRKX SRGAP1 ADGRG6

1.75e-06200455cb1f4b0d66da5b0466ff17b29e7034d451d93e4f
ToppCellPBMC-Mild-Myeloid-cDC-cDC-cDC_4|Mild / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.09)

DST DNAH10 SRGAP3 ADGRG6

1.72e-0515345491e9d70a5d3f6fd68c284ed0cc113f03d7d1e10b
ToppCellPBMC-Mild-Myeloid-cDC-cDC-cDC_4|Mild / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

DST DNAH10 SRGAP3 ADGRG6

1.72e-05153454f17f62646633cf95c810dcd5328978058741b276
ToppCell5'-Adult-Appendix-Hematopoietic-T_cells-gdT|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract

ODF2L ZNF782 ANKRD20A4P SRGAP3

1.76e-05154454d2aa24c593a1c0c6f186b74a18438b64b4e59701
ToppCellControl-B_naive-12|World / disease group and sub_cluster of B and Plasma cells(res = 0.5)

MPP1 ZNF585A DST SKP2

1.90e-051574544803f601c1ba43260aa09172acc7964aac2c8ccf
ToppCellSmart-seq2-tissue-resident_(Smart-seq2)-myeloid-myeloid_macrophage-microglial_cell|tissue-resident_(Smart-seq2) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

SRGAP2 HTRA1 DST SRGAP1

1.90e-05157454d4908cafd8870c1c225817f589ea2bce116ac7ab
ToppCellnormal_Lymph_Node-Myeloid_cells-pDCs|Myeloid_cells / Location, Cell class and cell subclass

DST DNAH10 CENPC POLB

2.84e-051744542274648b80dd74f3c948a779bba3391095964c34
ToppCell10x5'-lymph-node_spleen-Myeloid_Mac-Intestinal_macrophages|lymph-node_spleen / Manually curated celltypes from each tissue

MPP1 DST SRGAP1 ADGRG6

3.25e-051804547be7d7a6906fff6dbdecd9cb013d855aba4eda2a
ToppCellrenal_medulla_nuclei-Renal_AKI_(acute_kidney_injury)-Epithelial-Renal_corpuscle_epithelial_cell-glomerular_visceral_epithelial_cell-Podocyte|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 DST SRGAP1

3.32e-051814545bf7aa43f6e6ecce15c95928b91195544d6928c4
ToppCellrenal_medulla_nuclei-Renal_AKI_(acute_kidney_injury)-Epithelial-Renal_corpuscle_epithelial_cell-glomerular_visceral_epithelial_cell|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 DST SRGAP1

3.32e-051814548e751f5d7cd2d328ec0196d874e8a507e8c4e1a9
ToppCellwk_15-18-Hematologic-Meg-ery-Definitive_erythroblast|wk_15-18 / Celltypes from embryonic and fetal-stage human lung

MPP1 ATG9A ANKRD20A4P ANKRD20A1

3.39e-0518245493841f730ca1a735eaaf5f2ccbe5c45ab0e029d1
ToppCell10x_3'_v2v3-Non-neoplastic-Myeloid-TAM-MG-TAM-MG_pro-infl_I-E|10x_3'_v2v3 / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group

SRGAP2 HTRA1 NFIL3 GOLGA4

3.46e-05183454614a1c08cf6d01a4f1ed2fb816cd1a6e0c3207ce
ToppCellrenal_cortex_nuclei-Adult_normal_reference-Epithelial-Renal_corpuscle_epithelial_cell-glomerular_visceral_epithelial_cell-Podocyte|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 PRDM5 SRGAP1

3.46e-05183454eb559ae3ae252d9365c24ef557dd49b78ed6d898
ToppCellfacs-Thymus-Thymus_Epithelium-18m-Lymphocytic|Thymus / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

PCDH15 DRP2 DNAH10 KALRN

3.54e-05184454ea7a7e2bac46d4d2c31a5d576b38a032b5335062
ToppCellfacs-Thymus-Thymus_Epithelium-18m-Lymphocytic-thymocyte|Thymus / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

PCDH15 DRP2 DNAH10 KALRN

3.54e-051844542cbed6462fea2622871bb7e49b0df3d984239281
ToppCellfacs-Thymus-Thymus_Epithelium-18m-Lymphocytic-proliferating_thymocyte;_DN_to_DP_transition,_dividing_(some_are_Cd8+/_Cd4+,_some_undergoing_VDJ_recombination)|Thymus / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

PCDH15 DRP2 DNAH10 KALRN

3.54e-051844542b19a8c5f823e00812908b23e66bb4e563278aff
ToppCellBAL-Severe-Myeloid-cDC-cDC-cDC_11|Severe / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.09)

ANKRD20A3P DST ANKRD20A1 ADGRG6

3.54e-05184454667846c422cfa27e949a24844a305df859cb6760
ToppCellPrimary_Visual_cortex_(V1C)-Neuronal-Inh_GABAergic-i_Gaba_3-GABA_SST-Inh_L4-5_PVALB_TRIM67|Primary_Visual_cortex_(V1C) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

PCDH15 HTRA1 PRKX ADGRG6

3.54e-051844547f6c8912677764d438ab0555faca344d74c2f483
ToppCellrenal_cortex_nuclei-Hypertensive_with+without-CKD-Epithelial-Renal_corpuscle_epithelial_cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 DST SRGAP1

3.61e-05185454b848b63aff4d9dbb9e66a85876d4c7c6dacd0579
ToppCellControl-Myeloid-cDC1|World / Disease state, Lineage and Cell class

ANKRD20A2P ANKRD20A3P ANKRD20A4P ANKRD20A1

3.69e-051864543de803dee3ef10eb85a2b47d3f93385214e5b0ff
ToppCell10x_3'_v3-lymph_node_(10x_3'_v3)-myeloid-myeloid_dendritic-CD141-positive_myeloid_dendritic_cell|lymph_node_(10x_3'_v3) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

ANKRD20A3P DST SRGAP1 ADGRG6

3.85e-0518845478e79b8e298aa77c8c01320bab4fb1a00f11a772
ToppCellChildren_(3_yrs)-Immune-interstitial_macrophage_(C1Q_positive)-D032|Children_(3_yrs) / Lineage, Cell type, age group and donor

MPP1 SRGAP2 MYO7A SRGAP1

4.01e-051904542d54fca50593fbd11fe13fc2bfaf937a05db776d
ToppCellkidney_cells-Adult_normal_reference-Epithelial-Renal_corpuscle_epithelial_cell-glomerular_visceral_epithelial_cell|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 DST SRGAP1

4.26e-051934543eaa0461618582a1754400624350d269d24e750a
ToppCellFetal_29-31_weeks-Mesenchymal-matrix_fibroblast_1_cell|Fetal_29-31_weeks / Lineage, Cell type, age group and donor

PCDH15 DST KALRN SRGAP1

4.35e-05194454011e14d9ed1393275f892060e7708ffadcd0767f
ToppCellPCW_13-14-Mesenchymal-Mesenchymal_fibroblastic-mes_immature5_(6)|PCW_13-14 / Celltypes from embryonic and fetal-stage human lung

DST KALRN SRGAP3 ADGRG6

4.35e-05194454b1bb0f846d2865efdd9bc8842b16b9d069785882
ToppCellkidney_cells-Adult_normal_reference-Epithelial-Renal_corpuscle_epithelial_cell|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

HTRA1 DST SRGAP1 ADGRG6

4.35e-0519445443eb677a76634bb9a48a40e0d607c4936ae64bcc
ToppCellPCW_10-12-Mesenchymal-Mesenchymal_fibroblastic-mes_immature5_(6)|PCW_10-12 / Celltypes from embryonic and fetal-stage human lung

DST KALRN SRGAP3 ADGRG6

4.44e-051954540e55fa5b3cbeb7baee3d4ac272a3bf80381ec937
ToppCelltumor_Lung-T/NK_cells-Exhausted_Tfh|T/NK_cells / Location, Cell class and cell subclass

HTRA1 MYO7A SRGAP3 GOLGA4

4.53e-051964545a0b5aeff7e535781ea2a4c85799bb468afcb6f8
ToppCellCOPD-Endothelial-VE_Capillary_B|Endothelial / Disease state, Lineage and Cell class

PCDH15 ANKRD20A2P ANKRD20A3P ANKRD20A4P

4.62e-0519745430dbc05ea66892d2e18ff375ffa86d1db7bc4083
ToppCellPCW_13-14-Mesenchymal-Mesenchymal_fibroblastic-mes_immature3_(17)|PCW_13-14 / Celltypes from embryonic and fetal-stage human lung

DST KALRN SRGAP3 ADGRG6

4.62e-0519745431a1852911bda38543916585fda34255fd62a134
ToppCellBronchial-NucSeq-Immune_Myeloid-Macrophage_other-Macrophage_intermediate|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

MPP1 SRGAP2 NFIL3 SRGAP1

4.62e-05197454e2983ae16c72371fbf0e5c123de9f4d900724e5e
ToppCell3'-Parenchyma_lung-Epithelial-Airway_ciliated-ciliated_columnar_cell_of_tracheobronchial_tree-Multiciliated_(non-nasal)-Multiciliated_(non-nasal)_L.0.3.2.2|3' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

ODF2L CLSTN2 DNAH10 LMLN

4.62e-0519745474a2c6cb8fcfe53dd9a2b36492a16c58f38e51c9
ToppCellBronchial-NucSeq-Immune_Myeloid-Macrophage_other-Macrophage_intravascular|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

MPP1 SRGAP2 MYO7A SRGAP1

4.71e-05198454c7dbf24caae5c4ef285845d13055de9e07281bb3
ToppCellParenchymal-NucSeq-Immune_Myeloid-Dendritic_cell-DC_1|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

ANKRD20A2P ANKRD20A3P ANKRD20A4P VCPIP1

4.71e-05198454fa5c15a656d4132950092919600e270f1fd79abf
ToppCell(11)_FOXN4+-(2)_GFP_FOXI1|(11)_FOXN4+ / shred by cell type by condition

ODF2L MAB21L3 GOLGA4 LMLN

4.71e-0519845476d40b8c2f8399725b3a62ee2ae0896559cf91eb
ToppCell(10)_Ciliated-(2)_GFP_FOXI1|(10)_Ciliated / shred by cell type by condition

ODF2L MAB21L3 GOLGA4 LMLN

4.80e-0519945461b1ed2db71b96157b92b7535d1955a4033098da
ToppCellBrain_organoid-organoid_Tanaka_cellReport-2m-Neuronal-Neuron|2m / Sample Type, Dataset, Time_group, and Cell type.

KALRN PRKX SRGAP3 SUN2

4.89e-05200454a581f1704a87b0390e1e2ff85053367d85247755
ToppCellBrain_organoid-organoid_Tanaka_cellReport-2m-Neuronal-Intermediate|2m / Sample Type, Dataset, Time_group, and Cell type.

DST ABI2 SRGAP3 SRGAP1

4.89e-052004542a635694844ddabcd98462c5636a6f41a3f08a46
ToppCellBrain_organoid-organoid_Tanaka_cellReport-6m-Neuronal-Neuron|6m / Sample Type, Dataset, Time_group, and Cell type.

KALRN PRKX SRGAP3 SUN2

4.89e-05200454b5019b9d48f32cffd4645a5c0f3e0ac504ea8019
ToppCellmild-gd_T|World / Cohort 1 (10x PBMC) with disease condition, cell group and cell class

ODF2L ATM CENPC GOLGA4

4.89e-05200454109f673a4967ffa52270a0b4f818b3461288db44
ToppCell(53)_Lymphoid_DC|World / shred on Cell_type and subtype

ANKRD20A2P ANKRD20A3P SRGAP1 ANKRD20A1

5.70e-0520845430212cfacad94a7cc562a69efa73a31259851515
ToppCellAT2_cells-IPF_02|World / lung cells shred on cell class, cell subclass, sample id

ANKRD20A2P ANKRD20A3P ANKRD20A4P

3.13e-04131453ff4e618bd944f852bbd34438f740187aca82460f
ToppCellTCGA-Peripheral_Nervous_System-Primary_Tumor-Paraganglioma-Paraganglioma-3|TCGA-Peripheral_Nervous_System / Sample_Type by Project: Shred V9

ATM PRDM5 SKP2

3.42e-04135453ac20133d4a36f48338b45bffb13e842cb66f83ad
ToppCell10x5'-Lung-Myeloid_Mac-Intestinal_macrophages|Lung / Manually curated celltypes from each tissue

HTRA1 SRGAP1 ADGRG6

3.88e-041414537671d300b1722711fd2d8034b96a3aa7e3ccb560
ToppCellsaliva-Severe-critical_progression_d12-22_no-steroids-Lymphocytic-Lymphocytic_B-B_cell|Severe-critical_progression_d12-22_no-steroids / Compartment, severity and other cell annotations on 10x 3' data (130k)

ATG9A ANKRD20A8P CENPC

4.56e-0414945354c9c6282f5f5de43dfaf2972fab3e3dcf9838a3
ToppCellsaliva-Severe-critical_progression_d12-22_no-steroids-Lymphocytic-Lymphocytic_B|Severe-critical_progression_d12-22_no-steroids / Compartment, severity and other cell annotations on 10x 3' data (130k)

ATG9A ANKRD20A8P CENPC

4.56e-0414945314d2e8cab97108d8fa94e540c1957b73ed32dc73
ToppCell10x_3'_v3-thymus_(10x_3'_v3)-myeloid-myeloid_dendritic-myeloid_dendritic_cell|thymus_(10x_3'_v3) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

SRGAP2 ANKRD20A3P ANKRD20A4P

4.56e-0414945371d72a6e7b128ee96161e08f6a0d77be925e73a1
ToppCell343B-Lymphocytic-CD8+_Cytotoxic_T-cell-CD8+_Cytotoxic_T_cell_1|343B / Donor, Lineage, Cell class and subclass (all cells)

ATM ZNF782 POLB

4.56e-041494532a7f71da51c85e04de2123164914122480e60d66
ToppCell390C-Fibroblasts-Fibroblast-G-|Fibroblasts / Donor, Lineage, Cell class and subclass (all cells)

PCDH15 DST LMLN

4.83e-04152453ebce79e106bf1d84241f8dd3496ff1771f9666be
ToppCell390C-Fibroblasts-Fibroblast-G|Fibroblasts / Donor, Lineage, Cell class and subclass (all cells)

PCDH15 DST LMLN

4.83e-041524534a749d1b6d35fd55a8c42d7bd04b6ff5b11ce781
ToppCell5'-Parenchyma_lung-Epithelial-Epithelial_transtional-secretory-nasal_mucosa_goblet_cell-Goblet_(nasal)|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

PCDH15 MAB21L3 SRGAP3

4.93e-041534533240d4d690335ba22317b1f3d33f9ea069e93838
ToppCell5'-Parenchyma_lung-Epithelial-Epithelial_transtional-secretory-nasal_mucosa_goblet_cell|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

PCDH15 MAB21L3 SRGAP3

4.93e-04153453edf5d026e8e4c685b7c369d70894741bb2cd568e
ToppCell10x5'-Liver-Myeloid_Mac-Intestinal_macrophages|Liver / Manually curated celltypes from each tissue

DST SRGAP3 ADGRG6

5.21e-041564539a897fc79c4fae94c5f2e9012d65297f9225e5e3
ToppCellsevere_COVID-19-cDC|severe_COVID-19 / disease group, cell group and cell class (v2)

DST ANKRD20A1 ADGRG6

5.31e-04157453ec1978e07e2214048d015d8bb793c1d9991f6e37
ToppCellControl-B_naive-12|Control / disease group and sub_cluster of B and Plasma cells(res = 0.5)

MPP1 ZNF585A DST

5.41e-0415845341318f864770370ce77ed3fa4a84f76c0c22c482
ToppCellnormal_Pleural_Fluid-T/NK_cells-CD4+_Th|normal_Pleural_Fluid / Location, Cell class and cell subclass

HTRA1 ANKRD20A4P MYO7A

5.51e-04159453ebd840ac2b07e62086ee7b5bb01c21804a0fdc7b
ToppCellPND03-Mesenchymal-Mesenchymal_myocytic-Myofibroblast_vascular-Pericyte-Pericyte_prolif|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

CLSTN2 ABI2 ADGRG6

5.72e-0416145382ed45f144a07856fe92d37426c5f92e259a03a9
ToppCell356C-Lymphocytic-ILC-ILC-3|Lymphocytic / Donor, Lineage, Cell class and subclass (all cells)

HTRA1 ATG9A SRGAP3

5.92e-041634532dbdcbc4c187aad3db837d191cc78662a75dd0b5
ToppCell10x_3'_v2v3-Non-neoplastic-Myeloid-TAM-MG-TAM-MG_pro-infl_II-E|10x_3'_v2v3 / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group

SRGAP2 HTRA1 GOLGA4

5.92e-04163453a6e272e043859858084b8d4d96fa4ff9e6eca454
ToppCellnormal_Pleural_Fluid-T/NK_cells-CD4+_Th|T/NK_cells / Location, Cell class and cell subclass

HTRA1 ANKRD20A4P MYO7A

6.03e-04164453334f376350c9cf92611d0f75b2e18a102f4c116a
ToppCellfacs-Brain_Non-Myeloid-Cerebellum-3m-Epithelial-neuronal_stem_cell|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation

CDT1 ZNF585A DNAH10

6.14e-041654531703d3eb644b3c743ad3c5532b1d29ea010c79c8
ToppCell10x_3'_v3-thymus_(10x_3'_v3)-myeloid-myeloid_dendritic|thymus_(10x_3'_v3) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

ANKRD20A3P ANKRD20A4P SRGAP1

6.25e-04166453479391aa6c09aa070b716128ab51b8fec0aea22d
ToppCelldroplet-Heart-nan-18m-Mesenchymal-nan|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

ATM DRP2 PRDM5

6.25e-041664539adceb746e67e955fd8b3e0984f4eed44b64a270
ToppCellSmart-start-Cell-Wel_seq-Non-neoplastic-Myeloid-TAM-MG|Smart-start-Cell-Wel_seq / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group

SRGAP2 MAB21L3 ATM

6.36e-04167453942134bbabe9972fae80cbc4ed4e94da52f55dc3
ToppCellrenal_medulla_nuclei-Adult_normal_reference-Epithelial-Renal_corpuscle_epithelial_cell|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 DST

6.47e-04168453315ca578c945aeeb77acda2727f3e6db8b43f43e
ToppCellHippocampus-Neuronal-Excitatory-eN1(Slc17a7)|Hippocampus / BrainAtlas - Mouse McCarroll V32

ABI1 KALRN ABI2

6.47e-041684536db453cbbbaf4144a86fadcfa5805d33396713b5
ToppCellrenal_medulla_nuclei-Adult_normal_reference-Epithelial-Renal_corpuscle_epithelial_cell-glomerular_visceral_epithelial_cell-Podocyte|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 DST

6.47e-04168453e96859dbf51cf8c4def8ee8db132f4d874fb4381
ToppCelltumor_Lymph_Node_/_Brain-T/NK_cells-Exhausted_Tfh|T/NK_cells / Location, Cell class and cell subclass

SRGAP3 NFIL3 SRGAP1

6.58e-04169453625788d86f0ceebcf2653a251db1f1a9f9746d29
ToppCellAdult-Endothelial-endothelial_cell_of_vein-D175|Adult / Lineage, Cell type, age group and donor

ANKRD20A4P KALRN ADGRG6

6.58e-04169453e1f0298236e4a1c59077c14f0dd29a78fac12648
ToppCell5'-Parenchyma_lung-Epithelial-Airway_ciliated-ciliated_columnar_cell_of_tracheobronchial_tree-Multiciliated_(non-nasal)-Multiciliated_(non-nasal)_L.0.3.2.2|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

DNAH10 SRGAP3 LMLN

6.58e-04169453fba841664939c771881ba97f14ef1df6635c04ff
ToppCell10x_3'_v2v3-Non-neoplastic-Myeloid-TAM-MG-TAM-MG_pro-infl_II-B|10x_3'_v2v3 / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group

SRGAP2 NFIL3 GOLGA4

6.58e-041694530867528101767fc65e93b3561480bf830c50368d
ToppCellhealthy_donor-Myeloid-Monocytic-Developing_Neutrophil|healthy_donor / Disease condition, Lineage, Cell class and subclass

ANKRD20A4P DNAH10 ADGRG6

6.69e-04170453cfd7f29805b7c51666b0eaf269c36c96b8765a1a
ToppCellrenal_medulla_nuclei-Hypertensive_with+without-CKD-Epithelial-Renal_corpuscle_epithelial_cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 DST

6.92e-041724536c17a1e586a72d1bd80c20c06370429c61dc9f85
ToppCelldroplet-Lung-18m-Hematologic-myeloid-classical_monocyte-classical_monocyte_l2-17-52|18m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype

TRAPPC10 NFIL3 LMLN

6.92e-04172453ebeda7ef181cac0109be750a98e7589c615d2724
ToppCellrenal_medulla_nuclei-Hypertensive_with+without-CKD-Epithelial-Renal_corpuscle_epithelial_cell-glomerular_visceral_epithelial_cell-Podocyte|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

SRGAP2 HTRA1 SRGAP1

6.92e-04172453381ae1c3c07d0a424f43455ec571653b192a946a
ToppCellPND07-Mesenchymal-Mesenchymal_myocytic-Myofibroblast_vascular-Pericyte-Pericyte_prolif|PND07 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

CLSTN2 CWH43 ADGRG6

6.92e-0417245303a0aff6b7971093a4347b5ed12546d78374c56f
ToppCellPND28-Endothelial-Endothelial_blood-vessel-Microvascular_EC-CAP1-CAP1_prolif|PND28 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

CLSTN2 CDT1 KALRN

7.04e-0417345312f779b8dce79431b2d1002ba524dd3f9566aeb0
ToppCellPBMC-Severe-Myeloid-cDC-cDC-cDC_12|Severe / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

CDT1 DST ADGRG6

7.04e-041734539c7386bf0a899882c733f0b4921a96afde032a7d
ToppCellPBMC-Severe-Myeloid-cDC-cDC-cDC_12|Severe / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.09)

CDT1 DST ADGRG6

7.04e-04173453a55f310c533432e9e26e400026a5b47245152976
ToppCellmild_COVID-19_(asymptomatic)-cDC|mild_COVID-19_(asymptomatic) / disease group, cell group and cell class (v2)

ANKRD20A3P DST ADGRG6

7.04e-0417345371dc0051c87b84e3cf13cde8858166f2a474b5dc
ToppCell343B-Lymphocytic-NK_cells-NK_cell_E|Lymphocytic / Donor, Lineage, Cell class and subclass (all cells)

ATG9A KALRN SRGAP3

7.16e-04174453a1f745962a104c6f4b86b7e482da8755384c773a
ToppCellBasal_cells-Cryobiopsy_01|World / lung cells shred on cell class, cell subclass, sample id

ANKRD20A2P ANKRD20A3P ANKRD20A4P

7.16e-04174453a0060be3940043015dcc49a5157de5541aed24a1
ToppCellrenal_cortex_nuclei-CKD+DKD_normotensive-Endothelial-lymphatic_endothelial_cell-lymphatic_endothelial_cell_of_renal_cortex-lymphatic_endothelial_cell_of_renal_cortex|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

PRDM5 KALRN SRGAP3

7.28e-041754539a96a946db731ba24c9be34bedebf1f4a1372b9e
ToppCellPBMC-Severe-Lymphocyte-T/NK-NK_cell-NK_CD56bright|Severe / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

ATM DST SRGAP3

7.28e-04175453e219b61d6bc078d44ea7d06191d3462654d857a1
DiseaseUsher Syndrome

PCDH15 MYO7A

1.13e-054412C0271097
DiseaseUsher Syndrome, Type II

PCDH15 MYO7A

1.88e-055412C1568249
DiseaseUsher syndrome, type 1A

PCDH15 MYO7A

1.88e-055412C2931205
DiseaseUSHER SYNDROME, TYPE IB (disorder)

PCDH15 MYO7A

1.88e-055412C1848638
DiseaseUSHER SYNDROME, TYPE IA, FORMERLY

PCDH15 MYO7A

1.88e-055412C1848639
DiseaseUSHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY

PCDH15 MYO7A

1.88e-055412C1848640
DiseaseUsher syndrome type 1

PCDH15 MYO7A

1.88e-055412cv:C1568247
DiseaseUsher Syndrome, Type I

PCDH15 MYO7A

2.82e-056412C1568247
DiseaseHereditary retinal dystrophy

PCDH15 MYO7A

3.94e-057412C0154860
DiseaseUsher Syndrome, Type III

PCDH15 MYO7A

3.94e-057412C1568248
DiseaseUsher syndrome

PCDH15 MYO7A

3.94e-057412cv:C0271097
DiseaseNonsyndromic genetic hearing loss

PCDH15 MYO7A DIABLO

1.63e-0476413cv:C5680182
DiseaseNonsyndromic Deafness

PCDH15 MYO7A DIABLO

1.97e-0481413C3711374
Diseasewhite matter microstructure measurement

SRGAP2 ABI2 SRGAP3 SUN2 ADGRG6

1.99e-04390415EFO_0005674
Diseaseidiopathic scoliosis (implicated_via_orthology)

DNAH10 ADGRG6

2.23e-0416412DOID:0060250 (implicated_via_orthology)
Diseasehearing impairment

PCDH15 MYO7A DIABLO

3.46e-0498413C1384666
Diseasehippocampus volume change measurement, age at assessment

PCDH15 SUN2

7.47e-0429412EFO_0008007, EFO_0021492
DiseaseAutosomal dominant nonsyndromic hearing loss

MYO7A DIABLO

7.47e-0429412cv:C5779548
Diseasecholesteryl ester 22:6 measurement

SRGAP2 SRGAP3

9.10e-0432412EFO_0010350
Diseasecysteine-rich with EGF-like domain protein 1 measurement

SRGAP2 SRGAP3

9.10e-0432412EFO_0021870
DiseaseHereditary hearing loss and deafness

PCDH15 MYO7A DIABLO

1.10e-03146413cv:C0236038
Diseaseskin microbiome measurement

SRGAP2 SRGAP3

1.35e-0339412EFO_0801228
Diseaselung non-small cell carcinoma (is_marker_for)

HTRA1 ATM DIABLO

1.68e-03169413DOID:3908 (is_marker_for)
DiseaseMedulloblastoma

ATM SKP2

2.21e-0350412C0025149
DiseaseNonsyndromic Hearing Loss and Deafness, Autosomal Recessive

PCDH15 MYO7A

2.30e-0351412cv:CN043650
DiseaseChronic Lymphocytic Leukemia

ATM POLB

2.67e-0355412C0023434

Protein segments in the cluster

PeptideGeneStartEntry
VHQKEDHKEIVTNIQ

ANKRD20A1

751

Q5TYW2
VHQKEDHKEIVTNIQ

ANKRD20A8P

751

Q5CZ79
VHQKEDHKEIVTNIQ

ANKRD20A4P

751

Q4UJ75
VQIKIKHTRTQEVHH

ADGRG6

786

Q86SQ4
QIFSQKLVEHVKEHH

CDT1

296

Q9H211
NHISQTVDIHKEKVA

ABI1

91

Q8IZP0
HIQLVKLQVEEVHQL

DIABLO

186

Q9NR28
SHKAVVHIQVKDVNE

CLSTN2

141

Q9H4D0
NHISQTVDIHKEKVA

ABI2

91

Q9NYB9
SVKVVHERLQIQIHK

ODF2L

181

Q9ULJ1
FKRKDTLNVHVQVVH

PRDM5

441

Q9NQX1
TLNVHVQVVHERHKK

PRDM5

446

Q9NQX1
VHQKEDHKEIVTNIQ

ANKRD20A2P

751

Q5SQ80
KKVVAVHLHQTVQVD

INTS11

131

Q5TA45
HHQQQVDSIIKEHEV

GOLGA4

731

Q13439
QHEKIISQHQAVIIA

DST

3856

Q03001
DTEVINKVHLKANHV

LMLN

71

Q96KR4
KHVHATVVKVPEVNS

NFIL3

306

Q16649
SKAVHQVLDVVHEVL

KALRN

501

O60229
QAVEEVQKVVHHLTT

MAB21L3

26

Q8N8X9
IHSIVVQVQCINKKV

PCDH15

111

Q96QU1
VCKTILNHVLHVVKN

ATM

986

Q13315
VHQKEDHKEIVTNIQ

ANKRD20A3P

751

Q5VUR7
VTNAHVVTNKHRVKV

HTRA1

216

Q92743
VQAHEVHQKILATDV

CENPC

111

Q03188
RIVQTQKEHQICIHK

ATG9A

186

Q7Z3C6
TKFETVHQIHKQNKI

MPP1

361

Q00013
VHQIHKQNKIAILDI

MPP1

366

Q00013
IENVVKHVVLVHQSV

DNAH10

2986

Q8IVF4
LHQVVEQLQKVHFIT

POLB

211

P06746
HRVTIAEQVKHQTKC

DRP2

596

Q13474
QKVVIDHREVSEKIH

CWH43

656

Q9H720
VVRVVEALHQKNIVH

STK40

181

Q8N2I9
QAHVNEIIKTIIIHH

SRGAP1

676

Q7Z6B7
SQHVVKVDFLNRIHK

PHF12

346

Q96QT6
EKHVQVAVAHVSETI

SKP2

271

Q13309
IGVTEEQVHHIVKQA

SUN2

521

Q9UH99
QAHINEVIKTIIIHH

SRGAP3

676

O43295
QAHVNELIKTIIIQH

SRGAP2

661

O75044
QKSILIVHQKIHTGE

ZNF585B

561

Q52M93
EILVQKVVHTILHQT

VCPIP1

641

Q96JH7
IRLKQEQHVHNEKSV

PRKX

86

P51817
AHNDVVEVVVKHEAK

TNKS2

411

Q9H2K2
QKSILIVHQKIHTGE

ZNF585A

561

Q6P3V2
LHHKEEVIQHQTIQT

ZNF782

196

Q6ZMW2
HVEQIVVNVHFSIEK

TRAPPC10

621

P48553
EVEAIQHKTTQIFHK

MYO7A

1891

Q13402