Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionnucleoside-triphosphatase regulator activity

GRIPAP1 RAPGEF6 STARD8 TBC1D30 PLEKHG5 TIAM2 ARFGEF3 CAVIN4 ARRB1 DEF6 ARHGAP27 HERC2 SMCR8 ARAP2

3.18e-0550715114GO:0060589
GeneOntologyMolecularFunctionGTPase regulator activity

GRIPAP1 RAPGEF6 STARD8 TBC1D30 PLEKHG5 TIAM2 ARFGEF3 CAVIN4 ARRB1 DEF6 ARHGAP27 HERC2 SMCR8 ARAP2

3.18e-0550715114GO:0030695
GeneOntologyCellularComponentspectrin

SPTA1 SPTAN1 SPTB

3.07e-0591523GO:0008091
DomainNPIP

NPIPA1 NPIPA7 NPIPA5 NPIPA3 NPIPA2

6.52e-08141535IPR009443
DomainSpectrin

SPTA1 SPTAN1 SPTB DMD

3.40e-05231534PF00435
DomainSpectrin_repeat

SPTA1 SPTAN1 SPTB DMD

8.77e-05291534IPR002017
DomainSPEC

SPTA1 SPTAN1 SPTB DMD

1.30e-04321534SM00150
DomainSpectrin/alpha-actinin

SPTA1 SPTAN1 SPTB DMD

1.30e-04321534IPR018159
DomainCavin_fam

CAVIN4 CAVIN1

3.96e-0441532IPR026752
DomainPTRF_SDPR

CAVIN4 CAVIN1

3.96e-0441532PF15237
DomainZF_ZZ_2

ZZEF1 HERC2 DMD

4.02e-04181533PS50135
DomainZF_ZZ_1

ZZEF1 HERC2 DMD

4.02e-04181533PS01357
DomainZZ

ZZEF1 HERC2 DMD

4.02e-04181533PF00569
DomainZnf_ZZ

ZZEF1 HERC2 DMD

4.74e-04191533IPR000433
DomainZnF_ZZ

ZZEF1 HERC2 DMD

4.74e-04191533SM00291
DomainWW

MAGI1 PQBP1 ARHGAP27 DMD

5.87e-04471534PF00397
DomainWW

MAGI1 PQBP1 ARHGAP27 DMD

6.37e-04481534SM00456
DomainWW_DOMAIN_1

MAGI1 PQBP1 ARHGAP27 DMD

8.02e-04511534PS01159
DomainWW_DOMAIN_2

MAGI1 PQBP1 ARHGAP27 DMD

8.02e-04511534PS50020
DomainWW_dom

MAGI1 PQBP1 ARHGAP27 DMD

8.64e-04521534IPR001202
DomainBRK

CHD8 CHD6

9.79e-0461532SM00592
DomainBRK_domain

CHD8 CHD6

9.79e-0461532IPR006576
DomainEFhand_Ca_insen

SPTA1 SPTAN1

9.79e-0461532PF08726
DomainEF-hand_Ca_insen

SPTA1 SPTAN1

9.79e-0461532IPR014837
DomainBRK

CHD8 CHD6

9.79e-0461532PF07533
DomainPI3K_Ras-bd_dom

PIK3C2A PIK3C2G

1.36e-0371532IPR000341
DomainAPC_su10/DOC_dom

ZZEF1 HERC2

1.36e-0371532IPR004939
DomainDOC

ZZEF1 HERC2

1.36e-0371532PS51284
DomainPI3K_rbd

PIK3C2A PIK3C2G

1.36e-0371532SM00144
DomainANAPC10

ZZEF1 HERC2

1.36e-0371532PF03256
DomainPI3K_rbd

PIK3C2A PIK3C2G

1.36e-0371532PF00794
DomainPI3K_RBD

PIK3C2A PIK3C2G

1.36e-0371532PS51546
DomainAPC10

ZZEF1 HERC2

1.36e-0371532SM01337
PathwayREACTOME_INTERACTION_BETWEEN_L1_AND_ANKYRINS

SPTA1 SPTAN1 SPTB

4.01e-05101003MM15112
PathwayREACTOME_INTERACTION_BETWEEN_L1_AND_ANKYRINS

NRCAM SPTA1 SPTAN1 SPTB

6.47e-05311004M877
Pubmed

Novel retinal and cone photoreceptor transcripts revealed by human macular expression profiling.

NPIPA1 NPIPA5 NPIPA3 NPIPA2

4.65e-104163418055785
Pubmed

Kelch Domain of Gigaxonin Interacts with Intermediate Filament Proteins Affected in Giant Axonal Neuropathy.

SPTA1 SPTAN1 SPTB HNRNPM ZZEF1 DNAJC10 ALMS1 DMD NUP160 CUX1

2.14e-081871631026460568
Pubmed

SLFN11 promotes CDT1 degradation by CUL4 in response to replicative DNA damage, while its absence leads to synthetic lethality with ATR/CHK1 inhibitors.

SPTAN1 HNRNPM NUP205 PHF2 LIG4 DDX50 AATF HERC2 NUP160 PDZRN3

3.24e-072501631033536335
Pubmed

The spectrin-based membrane skeleton stabilizes mouse megakaryocyte membrane systems and is essential for proplatelet and platelet formation.

SPTA1 SPTAN1 SPTB

4.03e-074163321566095
Pubmed

Remarkable homology among the internal repeats of erythroid and nonerythroid spectrin.

SPTA1 SPTAN1 SPTB

4.03e-07416333862089
Pubmed

Spectrin alpha II and beta II isoforms interact with high affinity at the tetramerization site.

SPTA1 SPTAN1 SPTB

4.03e-074163312820899
Pubmed

A human MAP kinase interactome.

MAGI1 ZNF142 SPTAN1 HNRNPM CHD8 ARRB1 PIAS3 NAV3 CHD6 HERC2 DMD MBD5 CUX1

5.56e-074861631320936779
Pubmed

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

LARP6 ZSWIM5 SPTA1 SPTAN1 HNRNPM NUP205 SLC25A22 LIG4 ARRB1 BBX DNAJC10 DDX50 UMODL1 CFAP74 AATF BOD1L1 ISG20L2 CHD6 DMD ABCC2 CUX1 RAI1

1.16e-0614421632235575683
Pubmed

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

SASH1 BMS1 CHD8 ZZEF1 PLEKHG5 TIAM2 NUP205 NUAK2 PSME4 NUAK1 PDCD11 TMEM131L RAI1

1.43e-065291631314621295
Pubmed

Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man.

SPTA1 SPTAN1 SPTB

3.49e-06716333186715
Pubmed

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

SH3TC2 GRIPAP1 STARD8 TBC1D30 PHF2 NEK1 ALMS1 WDR11 MBD5 SCIN NUP160 PDZRN3

4.05e-064931631215368895
Pubmed

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

RAPGEF6 CHD8 ZZEF1 PLEKHG5 HDAC7 TIAM2 SLC25A22 DACT1 PSME4 UBN1 NUAK1 IER5L CCDC3 DEF6 PDCD11 HERC2 MBD5 RAI1

4.83e-0611051631835748872
Pubmed

POTE, a highly homologous gene family located on numerous chromosomes and expressed in prostate, ovary, testis, placenta, and prostate cancer.

POTEB2 POTEA POTEB

5.56e-068163312475935
Pubmed

Proteomic profiling of VCP substrates links VCP to K6-linked ubiquitylation and c-Myc function.

SPTAN1 CAPN1 BMS1 HNRNPM ELP1 CHD8 CBR1 NUP205 SLC25A22 NAMPT PSME4 UBN1 DDX50 WDR11 PIK3C2A PDCD11 AATF CAVIN1 HERC2 NUP160

5.92e-0613531632029467282
Pubmed

The in vivo Interaction Landscape of Histones H3.1 and H3.3.

ZNF813 CHD8 PHF2 BBX UBN1 NFATC2IP SGO2 BOD1L1 CHD6 HERC2 CUX1 RAI1 BRWD1

6.47e-066081631336089195
Pubmed

Cell organization, growth, and neural and cardiac development require αII-spectrin.

SPTA1 SPTAN1 SPTB

1.18e-0510163322159418
Pubmed

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

TICRR NEPRO BMS1 HNRNPM CHMP2B NUP205 DNAJC10 DDX50 NEMF PDCD11 SGO2 AATF ISG20L2 HERC2

1.49e-057591631435915203
Pubmed

LncRNAs-directed PTEN enzymatic switch governs epithelial-mesenchymal transition.

RAPGEF6 NRCAM SPTA1 HPSE2 IGSF10 ARRB1 BBX

1.53e-05168163730631154
Pubmed

Phosphatidylinositol 3-kinase regulates human immunodeficiency virus type 1 replication following viral entry in primary CD4+ T lymphocytes and macrophages.

PIK3C2A PIK3C2G CXCR4

2.16e-0512163312551992
Pubmed

Calpain-dependent alpha-fodrin cleavage at the sarcolemma in muscle diseases.

SPTAN1 CAPN1

2.18e-052163215948206
Pubmed

Effects on sperm morphology by alleles at the pink-eyed dilution locus in mice.

OCA2 HERC2

2.18e-0521632863229
Pubmed

Associations of OCA2-HERC2 SNPs and haplotypes with human pigmentation characteristics in the Brazilian population.

OCA2 HERC2

2.18e-052163228081795
Pubmed

A deletional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin Tokyo (beta 220/216).

SPTA1 SPTB

2.18e-05216321391962
Pubmed

Molecular characterization of radiation- and chemically induced mutations associated with neuromuscular tremors, runting, juvenile lethality, and sperm defects in jdf2 mice.

OCA2 HERC2

2.18e-052163210441737
Pubmed

Chaperone activity and prodan binding at the self-associating domain of erythroid spectrin.

SPTA1 SPTB

2.18e-052163215492010
Pubmed

Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.

SPTA1 SPTB

2.18e-05216328102379
Pubmed

Beta-spectrin Promiss-ao: a translation initiation codon mutation of the beta-spectrin gene (ATG --> GTG) associated with hereditary spherocytosis and spectrin deficiency in a Brazilian family.

SPTA1 SPTB

2.18e-05216329414314
Pubmed

Variations in both α-spectrin (SPTA1) and β-spectrin ( SPTB ) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosis.

SPTAN1 SPTB

2.18e-052163224193021
Pubmed

Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.

SPTA1 SPTB

2.18e-05216329005995
Pubmed

Identification of the molecular defect in the erythrocyte membrane skeleton of some kindreds with hereditary spherocytosis.

SPTA1 SPTB

2.18e-05216327104494
Pubmed

A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis.

SPTA1 SPTB

2.18e-05216326215583
Pubmed

MURC/Cavin-4 and cavin family members form tissue-specific caveolar complexes.

CAVIN4 CAVIN1

2.18e-052163219546242
Pubmed

Pleiotropy in microdeletion syndromes: neurologic and spermatogenic abnormalities in mice homozygous for the p6H deletion are likely due to dysfunction of a single gene.

OCA2 HERC2

2.18e-05216327604002
Pubmed

The effects of mutant p-alleles on the reproductive system in mice.

OCA2 HERC2

2.18e-05216324435358
Pubmed

Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis.

SPTA1 SPTB

2.18e-05216323580577
Pubmed

Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.

SPTA1 SPTB

2.18e-05216327883966
Pubmed

A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice.

OCA2 HERC2

2.18e-05216329689098
Pubmed

Spectrin Cosenza: a novel beta chain variant associated with Sp alphaI/74 hereditary elliptocytosis.

SPTA1 SPTB

2.18e-05216329163587
Pubmed

Identification of three novel spectrin alpha I/74 mutations in hereditary elliptocytosis: further support for a triple-stranded folding unit model of the spectrin heterodimer contact site.

SPTA1 SPTB

2.18e-05216328018926
Pubmed

αII-spectrin regulates invadosome stability and extracellular matrix degradation.

SPTA1 SPTAN1

2.18e-052163225830635
Pubmed

Phenotypic and molecular convergence of 2q23.1 deletion syndrome with other neurodevelopmental syndromes associated with autism spectrum disorder.

MBD5 RAI1

2.18e-052163225853262
Pubmed

Site-directed mutagenesis of alpha II spectrin at codon 1175 modulates its mu-calpain susceptibility.

SPTAN1 CAPN1

2.18e-05216328993318
Pubmed

Erythrocyte spectrin is comprised of many homologous triple helical segments.

SPTA1 SPTB

2.18e-05216326472478
Pubmed

Exosome-mediated improvement in membrane integrity and muscle function in dystrophic mice.

CAPN1 DMD

2.18e-052163233333294
Pubmed

A new serine/threonine protein kinase, Omphk1, essential to ventral body wall formation.

NUAK2 NUAK1

2.18e-052163216715502
Pubmed

Linkage and association analysis of spectrophotometrically quantified hair color in Australian adolescents: the effect of OCA2 and HERC2.

OCA2 HERC2

2.18e-052163218528436
Pubmed

Positive selection of a gene family during the emergence of humans and African apes.

NPIPA1 NPIPA8

2.18e-052163211586358
Pubmed

An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216).

SPTA1 SPTB

2.18e-05216322070088
Pubmed

Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population.

SH3TC2 GDAP1

2.18e-052163225429913
Pubmed

A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color.

OCA2 HERC2

2.18e-052163218252222
Pubmed

Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.

OCA2 HERC2

2.18e-052163218252221
Pubmed

Thrombosis and secondary hemochromatosis play major roles in the pathogenesis of jaundiced and spherocytic mice, murine models for hereditary spherocytosis.

SPTA1 SPTB

2.18e-05216329373273
Pubmed

Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse.

OCA2 HERC2

2.18e-05216321495987
Pubmed

Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia.

SPTA1 SPTB

2.18e-052163230198572
Pubmed

Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis.

SPTA1 SPTB

2.18e-05216328844207
Pubmed

Gender is a major factor explaining discrepancies in eye colour prediction based on HERC2/OCA2 genotype and the IrisPlex model.

OCA2 HERC2

2.18e-052163223601698
Pubmed

Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation.

SPTA1 SPTB

2.18e-05216322056132
Pubmed

Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis.

SPTA1 SPTB

2.18e-05216322346784
Pubmed

Further insight into the global variability of the OCA2-HERC2 locus for human pigmentation from multiallelic markers.

OCA2 HERC2

2.18e-052163234795370
Pubmed

β-Arrestin1 and distinct CXCR4 structures are required for stromal derived factor-1 to downregulate CXCR4 cell-surface levels in neuroblastoma.

ARRB1 CXCR4

2.18e-052163224452472
Pubmed

Variants at the OCA2/HERC2 locus affect time to first cutaneous squamous cell carcinoma in solid organ transplant recipients collected using two different study designs.

OCA2 HERC2

2.18e-052163228456133
Pubmed

Genotyping of five single nucleotide polymorphisms in the OCA2 and HERC2 genes associated with blue-brown eye color in the Japanese population.

OCA2 HERC2

2.18e-052163219472299
Pubmed

Spectrin cagliari. an Ala-->Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer.

SPTA1 SPTB

2.18e-05216328226774
Pubmed

Properties of human red cell spectrin heterodimer (side-to-side) assembly and identification of an essential nucleation site.

SPTA1 SPTB

2.18e-05216321634521
Pubmed

Interactions of the alpha-spectrin N-terminal region with beta-spectrin. Implications for the spectrin tetramerization reaction.

SPTAN1 SPTB

2.18e-05216329890967
Pubmed

Glycosylation of erythrocyte spectrin and its modification in visceral leishmaniasis.

SPTA1 SPTB

2.18e-052163222164239
Pubmed

Crystal structure and functional interpretation of the erythrocyte spectrin tetramerization domain complex.

SPTA1 SPTB

2.18e-052163220197550
Pubmed

A structural model of the erythrocyte spectrin heterodimer initiation site determined using homology modeling and chemical cross-linking.

SPTA1 SPTB

2.18e-052163217977835
Pubmed

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

GRIPAP1 SPTAN1 ALMS1 HERC2 DMD NUP160

2.27e-05120163631413325
Pubmed

Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1.

STARD8 BMS1 PDCD11 NUP160

4.11e-054116348724849
Pubmed

FBXL13 directs the proteolysis of CEP192 to regulate centrosome homeostasis and cell migration.

FBXL13 VWDE NUP205 NKX6-1

4.53e-0542163429348145
Pubmed

Reciprocal interaction between SIRT6 and APC/C regulates genomic stability.

HNRNPM ELP1 CHD8 NUP205 DNAJC10 DDX50 SGO2 AATF HERC2 NUP160

4.68e-054401631034244565
Pubmed

E3 ubiquitin ligase RNF123 targets lamin B1 and lamin-binding proteins.

TICRR USP22 TBC1D30 BMS1 HNRNPM ZZEF1 NUP205 IGSF10 CCDC87 BOD1L1 CHD6 POTEA RAI1

4.74e-057361631329676528
Pubmed

HIV-1 gp120-mediated apoptosis of T cells is regulated by the membrane tyrosine phosphatase CD45.

PIK3C2A PIK3C2G CXCR4

5.41e-0516163316524887
Pubmed

The carboxyterminal EF domain of erythroid alpha-spectrin is necessary for optimal spectrin-actin binding.

SPTA1 SPTB

6.53e-053163220585040
Pubmed

Abnormal spermiogenesis in two pink-eyed sterile mutants in the mouse.

OCA2 HERC2

6.53e-05316325565073
Pubmed

Interactions between HERC2, OCA2 and MC1R may influence human pigmentation phenotype.

OCA2 HERC2

6.53e-053163219208107
Pubmed

Anti-band 3 and anti-spectrin antibodies are increased in Plasmodium vivax infection and are associated with anemia.

SPTA1 SPTB

6.53e-053163229884876
Pubmed

A non-GPCR-binding partner interacts with a novel surface on β-arrestin1 to mediate GPCR signaling.

ARRB1 CXCR4

6.53e-053163232753481
Pubmed

Interferon-γ resets muscle cell fate by stimulating the sequential recruitment of JARID2 and PRC2 to promoters to repress myogenesis.

JARID2 DMD

6.53e-053163224327761
Pubmed

The ATP-dependent chromatin remodeling enzymes CHD6, CHD7, and CHD8 exhibit distinct nucleosome binding and remodeling activities.

CHD8 CHD6

6.53e-053163228533432
Pubmed

Spectrin's E2/E3 ubiquitin conjugating/ligating activity is diminished in sickle cells.

SPTA1 SPTB

6.53e-053163215929114
Pubmed

Changing patterns in cytoskeletal mRNA expression and protein synthesis during murine erythropoiesis in vivo.

SPTA1 SPTB

6.53e-05316321385865
Pubmed

HERC2-USP20 axis regulates DNA damage checkpoint through Claspin.

HERC2 CLSPN

6.53e-053163225355518
Pubmed

Inherited hemolytic disease in mice: a review and update.

SPTA1 SPTB

6.53e-05316326763106
Pubmed

Functional consequences of chemically-induced β-arrestin binding to chemokine receptors CXCR4 and CCR5 in the absence of ligand stimulation.

ARRB1 CXCR4

6.53e-053163228733085
Pubmed

Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations.

OCA2 HERC2

6.53e-053163223118974
Pubmed

Mapping the binding sites of human erythrocyte ankyrin for the anion exchanger and spectrin.

SPTAN1 SPTB

6.53e-05316322141335
Pubmed

Zinc Finger 280B regulates sGCα1 and p53 in prostate cancer cells.

ZNF280B GUCY1A1

6.53e-053163224236047
Pubmed

Aciculin and its relation to dystrophin: immunocytochemical studies in human normal and Duchenne dystrophy quadriceps muscles.

SPTB DMD

6.53e-053163210867799
Pubmed

The peptidomimetic CXCR4 antagonist TC14012 recruits beta-arrestin to CXCR7: roles of receptor domains.

ARRB1 CXCR4

6.53e-053163220956518
Pubmed

Ankyrin-independent membrane protein-binding sites for brain and erythrocyte spectrin.

SPTA1 SPTAN1

6.53e-05316322971657
Pubmed

The molecular mechanisms mediating class II PI 3-kinase function in cell physiology.

PIK3C2A PIK3C2G

6.53e-053163233387369
Pubmed

The complete amino acid sequence for brain beta spectrin (beta fodrin): relationship to globin sequences.

SPTAN1 SPTB

6.53e-05316328479293
Pubmed

The class II PI 3-kinase, PI3KC2α, links platelet internal membrane structure to shear-dependent adhesive function.

PIK3C2A PIK3C2G

6.53e-053163225779105
Pubmed

Regulation of ploidy and senescence by the AMPK-related kinase NUAK1.

NUAK2 NUAK1

6.53e-053163219927127
Pubmed

Developmental expression of brain beta-spectrin isoform messenger RNAs.

SPTAN1 SPTB

6.53e-05316321467942
Pubmed

Macrophage activation through CCR5- and CXCR4-mediated gp120-elicited signaling pathways.

PIK3C2A PIK3C2G CXCR4

6.55e-0517163312960231
Pubmed

Organization of focal adhesion plaques is disrupted by action of the HIV-1 protease.

SPTA1 SPTAN1 SPTB

7.83e-0518163312119179
Pubmed

The RNA-mediated estrogen receptor α interactome of hormone-dependent human breast cancer cell nuclei.

NEPRO TBC1D30 BMS1 CHD8 PQBP1 CEP55 PHF2 JARID2 ZNF800 ARRB1 BBX DDX50 WDR11 PIK3C2A PDCD11 AATF ISG20L2 CHD6 HERC2

8.12e-0514971631931527615
InteractionCENPA interactions

BMS1 NUP205 PHF2 BBX NFATC2IP PDCD11 SGO2 AATF ISG20L2 CHD6 NUP160 CUX1 RAI1 BRWD1

1.35e-0637715514int:CENPA
Cytoband16p13.11

NPIPA1 CEP20 NPIPA5 NPIPA3 NPIPA2

1.70e-0823163516p13.11
CytobandEnsembl 112 genes in cytogenetic band chr16p13

NPIPA1 NPIPA7 UBN1 CEP20 NPIPA5 NPIPA3 NPIPA2 CAPN15

1.53e-044261638chr16p13
Cytoband17p11.2

USP22 CCDC144CP SMCR8 RAI1 CCDC144A

2.71e-04159163517p11.2
CytobandEnsembl 112 genes in cytogenetic band chr17p11

USP22 CCDC144CP SMCR8 RAI1 CCDC144A

8.24e-042031635chr17p11
GeneFamilyEF-hand domain containing|Spectrins

SPTA1 SPTAN1 SPTB

6.55e-06710531113
GeneFamilyAnkyrin repeat domain containing|POTE ankyrin domain containing

POTEB2 POTEA POTEB

5.22e-05131053685
GeneFamilyZinc fingers ZZ-type|Lysine acetyltransferases

ZZEF1 HERC2 DMD

1.46e-0418105391
GeneFamilyCavins

CAVIN4 CAVIN1

1.99e-04410521326
GeneFamilyPhosphatidylinositol 3-kinase subunits

PIK3C2A PIK3C2G

9.14e-0481052831
GeneFamilyPleckstrin homology domain containing|Rho guanine nucleotide exchange factors|C2 domain containing

SPTB PLEKHG5 TIAM2 DEF6 ARHGAP27 ARAP2

1.28e-032061056682
GeneFamilyPDZ domain containing

MAGI1 RAPGEF6 TIAM2 PDZRN3 PDZD2

1.93e-0315210551220
GeneFamilyC2 domain containing|Calpains

CAPN1 CAPN15

3.34e-03151052975
GeneFamilyX-linked mental retardation|Angiotensin receptors

ZNF674 PQBP1 DMD

3.61e-03531053103
GeneFamilyUbiquitin specific peptidases

USP45 USP22 USP6

4.22e-03561053366
CoexpressionAtlasFacebaseRNAseq_e10.5_Neural Epithelium Flanking Eminence_top-relative-expression-ranked_1000

MAGI1 AHI1 MAGEL2 NRCAM ZSWIM5 GDAP1 CLVS1 ZIC3 CEP55 NUAK2 NEK1 ZNF800 NAMPT DNAJC10 ALMS1 CXCR4 DBF4 NEMF SCUBE3 CFAP74 BOD1L1 DMD CLSPN CUX1 BRWD1

4.21e-0898915325Facebase_RNAseq_e10.5_Neural Epithelium Flanking Eminence_1000
CoexpressionAtlasFacebaseRNAseq_e10.5_Neural Epithelium Overlying Lateral Eminence_top-relative-expression-ranked_1000

MAGI1 PIGB MAGEL2 NRCAM ZSWIM5 GDAP1 CHD8 ZIC3 CEP55 NUAK2 PHF2 ZNF800 PRDM9 ALMS1 DBF4 CCDC3 NEMF CHD6 DMD CLSPN CUX1 ARAP2

2.27e-0698315322Facebase_RNAseq_e10.5_Neural Epithelium Overlying Lateral Eminence_1000
CoexpressionAtlasfacebase_RNAseq_e10.5_Emin_LatNas_2500_K3

TICRR CACNB2 AHI1 NRCAM ZSWIM5 PQBP1 NUAK2 JARID2 LIG4 ZNF800 PRDM9 PSME4 ALMS1 DBF4 NEMF TMEM131L SGO2 CFAP74 BOD1L1 DMD CLSPN MBD5 CUX1 BRWD1

1.14e-05125715324facebase_RNAseq_e10.5_Emin_LatNas_2500_K3
CoexpressionAtlasFacebaseRNAseq_e10.5_Neural Epithelium Flanking Eminence_top-relative-expression-ranked_500_k-means-cluster#2

NRCAM ZSWIM5 GDAP1 CLVS1 ZIC3 CEP55

2.29e-05791536Facebase_RNAseq_e10.5_Neural Epithelium Flanking Eminence_500_K2
CoexpressionAtlasFacebaseRNAseq_e10.5_Neural Epithelium Overlying Central Eminence_top-relative-expression-ranked_1000

MAGI1 AHI1 MAGEL2 NRCAM ZSWIM5 GDAP1 CHD8 ZNF280B CLVS1 ZIC3 CEP55 NUAK2 JARID2 ZNF800 PRDM9 ALMS1 DMD CLSPN PDZRN3 ATG16L2

2.84e-0598615320Facebase_RNAseq_e10.5_Neural Epithelium Overlying Central Eminence_1000
CoexpressionAtlasfacebase_RNAseq_e10.5_NeuroEpith_central_2500_K4

MAGI1 TICRR CACNB2 AHI1 ZSWIM5 SPTAN1 ZNF280B AASDH CEP55 NUAK2 TTC7A JARID2 ZNF800 PRDM9 PSME4 ALMS1 NUAK1 BOD1L1 DMD TMEM143 CLSPN THAP6 CUX1 BRWD1

4.59e-05137015324facebase_RNAseq_e10.5_NeuroEpith_central_2500_K4
CoexpressionAtlasFacebaseRNAseq_e10.5_Neural Epithelium Overlying Central Eminence_top-relative-expression-ranked_500

MAGI1 AHI1 MAGEL2 NRCAM ZSWIM5 GDAP1 CLVS1 ZIC3 CEP55 NUAK2 ZNF800 PRDM9 DMD

6.46e-0549615313Facebase_RNAseq_e10.5_Neural Epithelium Overlying Central Eminence_500
CoexpressionAtlasFacebaseRNAseq_e10.5_Neural Epithelium Flanking Eminence_top-relative-expression-ranked_500

NRCAM ZSWIM5 GDAP1 CLVS1 ZIC3 CEP55 NUAK2 ZNF800 ALMS1 CXCR4 NEMF CFAP74 CLSPN

6.73e-0549815313Facebase_RNAseq_e10.5_Neural Epithelium Flanking Eminence_500
CoexpressionAtlasFacebaseRNAseq_e10.5_Neural Epithelium Overlying Central Eminence_top-relative-expression-ranked_100

NRCAM ZSWIM5 GDAP1 CLVS1 ZIC3 NUAK2

8.66e-051001536Facebase_RNAseq_e10.5_Neural Epithelium Overlying Central Eminence_100
CoexpressionAtlasfacebase_RNAseq_e10.5_Emin_LatNas_2500

TICRR CACNB2 AHI1 NRCAM ZSWIM5 PQBP1 NUAK2 JARID2 LIG4 ZNF800 PRDM9 PSME4 ALMS1 DBF4 NEMF TMEM131L SGO2 CFAP74 BOD1L1 DMD CLSPN MBD5 CUX1 BRWD1

1.22e-04145915324facebase_RNAseq_e10.5_Emin_LatNas_2500
ToppCelldroplet-Lung-30m-Hematologic-myeloid-classical_monocyte_proliferating-classical_monocyte_proliferating_l12-14|30m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype

ZSWIM5 CEP55 NUP205 ARFGEF3 DBF4 CCDC3 SGO2 CLSPN

5.35e-07192162852d0aa51e3b6ab3608a5f40bdde9f8134b3afd94
ToppCellsaliva-Severe-critical_progression_d28-40-Myeloid-Macrophage-macrophage,_alveolar-Macro_c6-VCAN|Severe-critical_progression_d28-40 / Compartment, severity and other cell annotations on 10x 3' data (130k)

PIGB STARD8 SPTB AASDH DEF6 TMEM131L TMEM143

2.02e-0616016278374ae912337947b2cc8d17d5840f306361fe1ff
ToppCellControl-Stromal_mesenchymal-Matrix_Fibroblast-MatrixFB|Control / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

CACNB2 NRCAM IGSF10 NWD2 NUAK1 NAV3 PDZRN3

4.41e-06180162708ae0f5d95c45feba68ad99788f7af7ff4c979af
ToppCellControl-Stromal_mesenchymal-Matrix_Fibroblast|Control / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

CACNB2 NRCAM IGSF10 NWD2 NUAK1 NAV3 PDZRN3

4.41e-0618016279b1de1b4711adbf9a423f4d2d08f3f4c78f1f8f4
ToppCellPCW_10-12-Immune_Lymphocytic-Immune_Lymphocytic_B-im_B_cell_(15)|PCW_10-12 / Celltypes from embryonic and fetal-stage human lung

SPTA1 LIG4 UMODL1 CXCR4 MICB ARHGAP27 ARAP2

4.58e-06181162751e4d6bfdbf414d8e30aee2e6f7492f4f7f54373
ToppCellControl-Classical_Monocyte-cMono_4|Control / Disease condition and Cell class

RNF19B NAB2 JARID2 NAMPT IER5L CXCR4 CAVIN1

4.58e-061811627f3e1d8fe5cf1eba19e51c3680a55306cae687fe9
ToppCelldroplet-Lung-LUNG-30m-Lymphocytic-Proliferating_NK|Lung / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TICRR FASLG CEP55 DBF4 SGO2 CLSPN KLHL4

4.75e-0618216270370b395ceb9d4d66f80cf60dd8c28ac60af5c7b
ToppCell3'-Child09-12-SmallIntestine-Mesenchymal-Pericytes-Pericyte|Child09-12 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

FBXL13 SASH1 SPTA1 GRM8 GUCY1A1 CCDC3 CAVIN1

6.29e-061901627136ca6da77a202874376af193a1dd71d810c76c4
ToppCellControl-Stromal_mesenchymal|Control / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

CACNB2 HPSE2 IGSF10 NWD2 CCDC3 DMD PDZRN3

6.51e-06191162714057205ddb9b4bbc582d1358d13cf36d979a61b
ToppCelldroplet-Lung-nan-3m-Myeloid-dendritic_cell|Lung / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TICRR PIGB CEP55 ESYT3 TMEM131L SCIN

2.00e-05152162677b319f594d5e4df29034bbf69c7490076f89dd3
ToppCellChildren_(3_yrs)-Mesenchymal-airway_smooth_muscle_cell-D032|Children_(3_yrs) / Lineage, Cell type, age group and donor

TICRR SH3TC2 CACNB2 HPSE2 NWD2 DMD

2.23e-051551626cd7d95cbcad248670e531d80bb83c55e36ebc573
ToppCellprimary_visual_cortex-Neuronal-glutamatergic_neuron-L2/3_IT-L2/3_IT_VISp_Adamts2|primary_visual_cortex / Per Region, Lineage, Cell class, Cell type, Cell subtype

STARD8 TIAM2 NWD2 GUCY1A1 CPNE4 PDZRN3

2.31e-0515616262cd007b423c2395c5ce331902e7f27c805755eb3
ToppCell3'-GW_trimst-1.5-LargeIntestine-Mesenchymal-stromal_related|GW_trimst-1.5 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

CACNB2 CLVS1 SLC25A22 CAVIN4 CCDC144A PDZD2

2.76e-0516116268aaca49b53a551395f4025ac4e535c7b0ce41a49
ToppCellVE-mono3|VE / Condition, Cell_class and T cell subcluster

NRCAM USP6 ESYT3 NUAK1 NAV3 SCIN

2.76e-0516116267df3fefc55ab43b897fc78d1f0c7383b10ac33d5
ToppCell3'-GW_trimst-1.5-LargeIntestine-Mesenchymal-stromal_related-ICC|GW_trimst-1.5 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

CACNB2 CLVS1 SLC25A22 CAVIN4 CCDC144A PDZD2

2.76e-051611626deb10628d258fb813c293f81fb71be8e383dc82a
ToppCellVE-mono3-|VE / Condition, Cell_class and T cell subcluster

NRCAM USP6 ESYT3 NUAK1 NAV3 SCIN

2.76e-0516116264e45bf7eceb0ee30dec4d8852778366776ea5a8f
ToppCellChildren_(3_yrs)-Mesenchymal-airway_smooth_muscle_cell-D046|Children_(3_yrs) / Lineage, Cell type, age group and donor

CACNB2 NRCAM HPSE2 DMD PDZRN3 KLHL4

3.06e-051641626e3983f655cdba308fb192182829f17bef99ce0ba
ToppCellPND03-Immune-Immune_Lymphocytic_T/NK-Lymphocytic_ILC-NK-ILC-ILC_G2M|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

TICRR CEP55 DEF6 SGO2 CLSPN FAM83A

3.17e-05165162626c750f10f6401752e2e63d91dc844c81b29d735
ToppCellrenal_medulla_nuclei-Renal_AKI_(acute_kidney_injury)-Epithelial-Proximal_tubule_epithelial_cell-kidney_proximal_tubule_epithelial_cell_cycling-Cycling_Proximal_Tubule_Epithelial_Cell_low-phase|Renal_AKI_(acute_kidney_injury) / Celltypes from Cells and Nuclei per compartment and clinical group

SLCO6A1 ESYT3 PIAS3 CEP20 GUCY1A1 DEF6

3.28e-05166162643f84d3cd58e93ce00c241656c4cba27604b4932
ToppCell5'-GW_trimst-2-LymphNode-Hematopoietic-B_cells-Pro-B|GW_trimst-2 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

OR7A5 SPTA1 TTC7A LIG4 UMODL1 CXCR4

3.50e-051681626c833e3311af2582787d3ff2ad59d802fff865f8f
ToppCellControl-Classical_Monocyte-cMono_4|Classical_Monocyte / Disease condition and Cell class

NAB2 JARID2 NAMPT IER5L CXCR4 CAVIN1

3.74e-0517016269e328e1f904c77dcce8aee4df775d7f0ac725775
ToppCellFetal_29-31_weeks-Mesenchymal-airway_smooth_muscle_cell-D150|Fetal_29-31_weeks / Lineage, Cell type, age group and donor

CACNB2 HPSE2 GUCY1A1 CCDC3 DMD PDZRN3

5.31e-05181162625915e2500430a902db37d79a749ce2990b69810
ToppCellrenal_cortex_nuclei-Hypertensive_with+without-CKD|renal_cortex_nuclei / Celltypes from Cells and Nuclei per compartment and clinical group

CACNB2 IL1RAPL2 CCDC3 CPNE4 CUX1 PDZD2

5.31e-051811626c80ffa2ded5975a88e9a1a7d333196f95237bf0a
ToppCellfacs-Thymus-Thymus_Epithelium-18m-Lymphocytic-thymocyte|Thymus / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

NRCAM SPTA1 ARFGEF3 PIK3C2G NAV3 DMD

5.81e-0518416262cbed6462fea2622871bb7e49b0df3d984239281
ToppCellfacs-Thymus-Thymus_Epithelium-18m-Lymphocytic|Thymus / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

NRCAM SPTA1 ARFGEF3 PIK3C2G NAV3 DMD

5.81e-051841626ea7a7e2bac46d4d2c31a5d576b38a032b5335062
ToppCellControl-Neu_4|World / 5 Neutrophil clusters in COVID-19 patients

TRIT1 DDX50 PIK3C2A TMEM131L SGO2 NPIPA3

5.81e-051841626ce7f044956613118ee2e9fb6af2455c3166cb414
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

NRCAM SPTA1 ARFGEF3 PIK3C2G NAV3 DMD

5.81e-0518416262b19a8c5f823e00812908b23e66bb4e563278aff
ToppCell10x3'2.3-week_12-13-Mesenchymal_myocytic-stroma-muscle|week_12-13 / cell types per 3 fetal stages;per 3',per 5'

MAGI1 CLVS1 CCDC3 DMD SCIN NPIPA2

5.99e-0518516260094f9baddb20214d2a2c166f1637d1a9cf1169a
ToppCellCV-Healthy-7|Healthy / Virus stimulation, Condition and Cluster

TRIT1 NPIPA7 WDR11 TMEM131L SMCR8 RAI1

5.99e-0518516261979d189c204f4c2893e3170a514ee7d5523406c
ToppCellfacs-Skin-Telogen-3m-Epithelial-actively_dividing_stem_cell|Skin / Skin_Bladder_Kidney_Mammary_Gland - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TICRR HPSE2 CEP55 DBF4 SGO2 CLSPN

6.17e-0518616269feef5936985e936b3d88f9d1bb012abb6468570
ToppCellfacs-Skin-Telogen-3m-Epithelial-keratinocyte_stem_cell|Skin / Skin_Bladder_Kidney_Mammary_Gland - method, tissue, subtissue, age, lineage, cell ontology and free annotation

TICRR HPSE2 CEP55 DBF4 SGO2 CLSPN

6.17e-05186162689f5b06bc56674af304912d481ac697c7c870904
ToppCelldroplet-Heart-nan-18m-Mesenchymal-smooth_muscle_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

GUCY1A1 MYLK4 CCDC3 SCUBE3 NKX6-1 DMD

6.36e-05187162659313a47a6012b2413d7d3673bb05fb7e49fd88f
ToppCelldroplet-Heart-nan-18m-Mesenchymal-smooth_muscle_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

GUCY1A1 MYLK4 CCDC3 SCUBE3 NKX6-1 DMD

6.36e-0518716262591fe1552cd10925ad1d8d1f062a057ce6bdad9
ToppCellControl-Fibroblasts-Other_FB|Control / group, cell type (main and fine annotations)

CACNB2 NRCAM HPSE2 NAV3 DMD PDZRN3

6.36e-051871626bd3739c4a52aa1ba5deffd778e113a9800f7e158
ToppCell5'-Airway_Nasal-Endothelial-Blood_vessel_EC-vein_endothelial_cell|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

NRCAM GDAP1 CHD8 DACT1 CCDC3 ABCC2

6.55e-051881626524d1d928c9386acf20e53d31894107dd7290dc7
ToppCell5'-Airway_Nasal-Endothelial-Blood_vessel_EC-vein_endothelial_cell-EC_venous_systemic-EC_venous_systemic_L.2.2.0.0|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

NRCAM GDAP1 CHD8 DACT1 CCDC3 ABCC2

6.55e-0518816261b57995d70cf81212e8d46dfaf44dbaf9c7bc4d5
ToppCell5'-Airway_Nasal-Endothelial-Blood_vessel_EC|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

NRCAM GDAP1 CHD8 DACT1 CCDC3 ABCC2

6.55e-051881626cd2d1f8e43c252dd8730a5758458ef63e7ffc836
ToppCell5'-Airway_Nasal-Endothelial-Blood_vessel_EC-vein_endothelial_cell-EC_venous_systemic|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

NRCAM GDAP1 CHD8 DACT1 CCDC3 ABCC2

6.55e-051881626f5a2f324f3f6c5078d57130392d3f1ba74f29094
ToppCell10x5'v1-week_12-13-Mesenchymal_osteo-stroma-chondrocyte|week_12-13 / cell types per 3 fetal stages;per 3',per 5'

MAGEL2 TIAM2 DACT1 SCUBE3 CAVIN1 PDZD2

6.55e-051881626c9270517e6940e9793586f67f02431210552f278
ToppCell5'-Adult-SmallIntestine-Mesenchymal-myocytic-myofibroblast_(RSPO2+)|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract

CACNB2 HPSE2 IL1RAPL2 CCDC3 DMD PDZRN3

6.55e-051881626879de94924de978478696fc7838e05a4d795b905
ToppCell5'-Airway_Nasal-Endothelial|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

NRCAM GDAP1 CHD8 DACT1 CCDC3 ABCC2

6.55e-0518816266c9d5e4014f807149328ff4eabd5e86dfe18094d
ToppCellPCW_07-8.5-Epithelial-Epithelial_airway-epi_proximal_progenitor1_(6)|PCW_07-8.5 / Celltypes from embryonic and fetal-stage human lung

NRCAM GRM8 VWDE ARFGEF3 DMD ARAP2

6.74e-0518916267659c7bbd58ee959a159294fb8d17317bbcc5681
ToppCellCOVID-19-kidney-Proliferating_T_cell|COVID-19 / Disease (COVID-19 only), tissue and cell type

TICRR SPTA1 CEP55 DEF6 SGO2 CLSPN

7.15e-051911626bae388e0e9447d576e68465d73d8313ef6925ffa
ToppCellMesenchymal-vascular_smooth_muscle_cell|World / Lineage, Cell type, age group and donor

CACNB2 SPTB GUCY1A1 CCDC3 DMD PDZRN3

7.15e-051911626fd89fbc62aa1c73e0f659991e3bd726a0c97bd68
ToppCellPND10-Mesenchymal-Mesenchymal_myocytic-Myofibroblast_vascular-VSMC-VSMC_mature|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

HPSE2 GUCY1A1 MYLK4 SCUBE3 CAVIN1 DMD

7.35e-05192162626d9207e72bbef5e0046de511e2c9ff752b726f3
ToppCellrenal_cortex_nuclei-Adult_normal_reference-Epithelial-Collecting_tubule_epithelial_cell-kidney_collecting_duct_principal_cell-Cortical_Collecting_Duct_Principal_Cell|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

AHI1 NRCAM NUAK2 IL1RAPL2 PIK3C2G SCIN

7.35e-051921626bae236c9f1fac77bce28d0a9cf090100d391ff77
ToppCellNeuron-Postmitotic-Inhibitory_Neuron-SST-MGE1-4|World / Primary Cells by Cluster

MAGI1 CXCR4 TMEM131L CHD6 PDZRN3 CUX1

7.57e-0519316262eb6e4cff4fe3ce564c1581f6f7df4834895aaa9
ToppCellPND10-Mesenchymal-Mesenchymal_myocytic-Myofibroblast_vascular-VSMC|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

HPSE2 GUCY1A1 MYLK4 SCUBE3 CAVIN1 DMD

7.57e-0519316267fc3ab7261c88c1df71744bf5b17e8e46c4300e0
ToppCellLPS-IL1RA+antiTNF-Stromal_mesenchymal-Matrix_Fibroblast-MatrixFB|LPS-IL1RA+antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

CACNB2 NRCAM IGSF10 NUAK1 CCDC3 PDZRN3

7.57e-051931626fb28717fadd06c3840636d25409ce80c9254bd34
ToppCellFrontal_cortex-Neuronal-Inhibitory-iN1(Gad1Gad2_Th)-Sst-Inhibitory_Neuron.Gad1Gad2.Sst-Nr2f2_(MGE-derived_cortical_interneurons--Martinotti_cells)|Frontal_cortex / BrainAtlas - Mouse McCarroll V32

FASLG VWDE ESYT3 SCIN

7.68e-05621624a20620a8869721ea62984c2022ee1b484b455824
ToppCellFrontal_cortex-Neuronal-Inhibitory-iN1(Gad1Gad2_Th)-Sst-Inhibitory_Neuron.Gad1Gad2.Sst-Nr2f2_(MGE-derived_cortical_interneurons--Martinotti_cells)-|Frontal_cortex / BrainAtlas - Mouse McCarroll V32

FASLG VWDE ESYT3 SCIN

7.68e-05621624ee694c06bcd924b4ddf744178ba3a99e04eed51b
ToppCellrenal_cortex_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Myocytic_interstitial_cell-Vascular_Smooth_Muscle_Cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

CACNB2 HPSE2 CCDC3 TMEM131L CAVIN1 DMD

7.79e-0519416265c3b2b05d1e4f146551fe4c920263d8e6ca34de3
ToppCellPND28-Mesenchymal-Mesenchymal_myocytic-Myofibroblast_vascular|PND28 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

GUCY1A1 MYLK4 SCUBE3 CAVIN1 DMD PDZD2

7.79e-051941626aaecde88bd54134a938e76cdf059c1c2653e4e77
ToppCellrenal_cortex_nuclei-Hypertensive_with+without-CKD-Mesenchymal-Myocytic_interstitial_cell-Vascular_Smooth_Muscle_Cell-|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

CACNB2 HPSE2 CCDC3 TMEM131L CAVIN1 DMD

7.79e-051941626ab9cad697f9209d2889bc02b43b502dfeb2ebfef
ToppCellIPF-Endothelial-VE_Peribronchial|World / Disease state, Lineage and Cell class

MAGI1 SASH1 NUAK1 CCDC3 NAV3 CAVIN1

8.01e-051951626120296531bbc8080dcabacbd64733cc1dc34603a
ToppCellIPF-Endothelial-VE_Peribronchial|IPF / Disease state, Lineage and Cell class

MAGI1 SASH1 NUAK1 CCDC3 NAV3 CAVIN1

8.01e-0519516262c3ad3cb79f11119ac69c413a938d21199145040
ToppCellCOVID-19-Fibroblasts-Alveolar_FB|COVID-19 / group, cell type (main and fine annotations)

CACNB2 NRCAM NUAK1 GUCY1A1 NAV3 PDZRN3

8.01e-051951626603050beeb33c331d4b2e3fa46cae3f3e0e4bdc7
ToppCellCOVID-19-T_cells-Cycling_NK/T_cells|COVID-19 / group, cell type (main and fine annotations)

TICRR SPTA1 SPTB CEP55 SGO2 CLSPN

8.01e-051951626764ed100c28d9bc93ee5ecabc5291c8f184d78da
ToppCellBronchial-NucSeq-Stromal-Myofibroblastic-Muscle_smooth_airway_ASM|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

CACNB2 NRCAM HPSE2 CCDC3 PDZRN3 KLHL4

8.24e-0519616269830fb3da7a60f65ad463e9054bb77c06b025e4d
ToppCellTracheal-NucSeq-Stromal-Myofibroblastic|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

CACNB2 NRCAM HPSE2 CCDC3 PDZRN3 KLHL4

8.71e-051981626c12e7511628db819a52959bb68580e27c00c2e41
ToppCellTracheal-NucSeq-Stromal-Myofibroblastic-Muscle_smooth_airway_ASM|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

CACNB2 NRCAM HPSE2 CCDC3 PDZRN3 KLHL4

8.71e-05198162622e766df1276c5b14aa0d83f434f47140ebb98ea
ToppCellCOVID-19_Mild-Neu_4|World / 5 Neutrophil clusters in COVID-19 patients

SASH1 NPIPA8 NUAK1 NPIPA5 NPIPA2

9.07e-0512416255ef9eb806fb2c8ee5aae0a75503d244b08ee10d4
ToppCellLPS_IL1RA-Endothelial-Endothelial-Gen_Cap|LPS_IL1RA / Treatment groups by lineage, cell group, cell type

USP22 SPTAN1 PLEKHG5 HDAC7 PIK3C2A BRWD1

9.21e-052001626dccec522ab0d7fff62ad6273b02aa9022dbbb8eb
ToppCellCOVID-19-kidney-Mito-rich_Int|kidney / Disease (COVID-19 only), tissue and cell type

HCN4 HPSE2 PRDM9 CPNE4 DMD

1.09e-04129162557b705106aec7bbfc587de1ccd4f2335fc44dd6f
ToppCellLPS_only-Endothelial-Endothelial-FOXM1|LPS_only / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

TICRR TIAM2 CEP55 SGO2 KLHL4

1.31e-0413416254d8f7ddad02fe76a614771e115ebb8e04623ba85
ToppCellPND01-03-samps-Mesenchymal-Pericyte-pericyte_E|PND01-03-samps / Age Group, Lineage, Cell class and subclass

MAGEL2 SPTA1 GUCY1A1 CXCR4 PDZD2

1.35e-04135162535928195cf34f055b353562c96f451aef2344d64
ComputationalGenes in the cancer module 67.

MAGEL2 ZSCAN31 SPTA1 DACT1 NEK1 CPNE4 ARAP2 PDZD2 KLHL4

7.29e-05227859MODULE_67
Drugsulindac; Up 200; 100uM; MCF7; HG-U133A

AHI1 SASH1 NAB2 GDAP1 GRM8 ARRB1 DNAJC10 CXCR4 CFAP74 BRWD1

9.62e-0719815310168_UP
DiseaseSKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 1

OCA2 HERC2

2.67e-0521532227220
DiseaseSKIN/HAIR/EYE PIGMENTATION 1, BLUE/NONBLUE EYES

OCA2 HERC2

2.67e-0521532cv:C1856895
DiseaseCardiomyopathy, Dilated

FASLG CAVIN4 ALMS1 DMD

1.13e-04481534C0007193
DiseaseCardiomyopathy, Familial Idiopathic

CPT2 FASLG ALMS1 DMD

1.33e-04501534C1449563
DiseaseMalignant neoplasm of breast

STARD8 NRCAM ZSWIM5 SPTAN1 ELP1 OCA2 HDAC7 ZNF404 IL1RAPL2 CXCR4 BOD1L1 CAVIN1 HERC2 DMD CLSPN CUX1

1.53e-04107415316C0006142
Diseasesuntan, skin pigmentation

OCA2 HERC2

1.59e-0441532EFO_0003784, EFO_0004279
DiseaseHereditary elliptocytosis

SPTA1 SPTB

1.59e-0441532cv:C0013902
Diseasehereditary spherocytosis (is_implicated_in)

SPTA1 SPTB

2.64e-0451532DOID:12971 (is_implicated_in)
DiseaseHereditary spherocytosis

SPTA1 SPTB

2.64e-0451532cv:C0037889
DiseaseAnemia, hereditary spherocytic hemolytic

SPTA1 SPTB

2.64e-0451532C0221409
Diseaseretinal layer thickness measurement

NPIPA1 OCA2 PIK3C2A NPIPA2

2.70e-04601534EFO_0600002
DiseaseElliptocytosis, Hereditary

SPTA1 SPTB

3.95e-0461532C0013902
Diseaseprimary ciliary dyskinesia (is_implicated_in)

CFAP74 BRWD1

3.95e-0461532DOID:9562 (is_implicated_in)
Diseaseinsulin measurement

SCP2D1-AS1 LARP6 SASH1 TBC1D30 HDAC7 MICB CHD6

5.07e-042671537EFO_0004467
DiseaseCHARGE syndrome (implicated_via_orthology)

CHD8 CHD6

5.51e-0471532DOID:0050834 (implicated_via_orthology)
Diseaseresponse to 5-fluorouracil, response to antineoplastic agent

SCIN ARAP2

5.51e-0471532GO_0036275, GO_0097327
Diseasewellbeing measurement, alcohol consumption measurement

DACT1 GUCY1A1 CCDC3 CPNE4

6.03e-04741534EFO_0007869, EFO_0007878
DiseaseBrugada syndrome

CACNB2 HCN4

7.33e-0481532cv:C1142166
DiseaseHereditary spherocytosis

SPTA1 SPTB

7.33e-0481532C0037889
Diseaseleptin measurement

SPTB ZNF800 CPNE4 PDZD2

8.48e-04811534EFO_0005000
DiseaseAutism Spectrum Disorders

CHD8 JARID2 NEMF RAI1

1.02e-03851534C1510586
DiseasePRADER-WILLI SYNDROME

MAGEL2 HERC2

1.17e-03101532176270
Diseasehair colour measurement, eye colour measurement, skin pigmentation measurement

OCA2 HERC2

1.17e-03101532EFO_0007009, EFO_0007822, EFO_0009764
DiseasePrader-Willi syndrome

MAGEL2 HERC2

1.17e-03101532cv:C0032897
DiseaseEczema

AHI1 FASLG ZNF800 MICB CAVIN1 ARHGAP27 RAI1

1.21e-033101537HP_0000964
DiseaseOther specified cardiac arrhythmias

CACNB2 HCN4

1.42e-03111532C0348626
DiseaseNodal rhythm disorder

CACNB2 HCN4

1.42e-03111532C0264893
Diseasepigmentation disease (is_implicated_in)

OCA2 HERC2

1.42e-03111532DOID:10123 (is_implicated_in)
DiseaseEctopic rhythm

CACNB2 HCN4

1.42e-03111532C1399226
DiseaseCARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)

CACNB2 HCN4

1.42e-03111532C2748542
Diseaseretinal nerve fibre layer thickness measurement

NPIPA1 OCA2 NPIPA2

1.45e-03431533EFO_0600004
Diseaseinterleukin 17 measurement

TTC7A NAV3 NUP160

1.65e-03451533EFO_0008174
DiseaseRoyer Syndrome

MAGEL2 HERC2

1.70e-03121532C0265222
DiseaseGastrointestinal Diseases

CHD8 ABCC2

1.70e-03121532C0017178
DiseaseFunctional Gastrointestinal Disorders

CHD8 ABCC2

1.70e-03121532C0559031
DiseaseCholera Infantum

CHD8 ABCC2

1.70e-03121532C1565321
DiseaseQT interval

CACNB2 CAVIN4 TMEM131L MBD5 NUP160 PDZRN3 CUX1 RAI1 BRWD1

1.95e-035341539EFO_0004682
Diseaseplatelet component distribution width

SH3TC2 AHI1 STARD8 APOA5 SPTA1 ZZEF1 HDAC7 TMEM131L CAVIN1 CUX1 BRWD1

2.00e-0375515311EFO_0007984
Diseasehematologic cancer (implicated_via_orthology)

PIAS3 CUX1

2.01e-03131532DOID:2531 (implicated_via_orthology)
Diseasephosphatidylcholine 40:7 measurement

NPIPA1 NPIPA2

2.01e-03131532EFO_0021477
DiseaseBrugada Syndrome 1

CACNB2 HCN4

2.01e-03131532C4551804
DiseaseCharcot-Marie-Tooth disease type 4

SH3TC2 GDAP1

2.01e-03131532cv:C4082197
DiseasePrader-Willi Syndrome

MAGEL2 HERC2

2.01e-03131532C0032897
Diseasecholesteryl ester 20:3 measurement

APOA5 NPIPA1 NPIPA2

2.11e-03491533EFO_0010347
Diseaseasymmetric dimethylarginine measurement

SCP2D1-AS1 ZZEF1

2.33e-03141532EFO_0010463
DiseaseSinus Node Dysfunction (disorder)

CACNB2 HCN4

2.68e-03151532C0428908
Diseaseautism spectrum disorder (is_implicated_in)

AHI1 MBD5

3.06e-03161532DOID:0060041 (is_implicated_in)
Diseaseomega-3 polyunsaturated fatty acid measurement

AHI1 APOA5 CXCR4 BRWD1

3.37e-031181534EFO_0010119
Diseaseresponse to efavirenz, virologic response measurement

GRM8 IGSF10 PIK3C2A

3.42e-03581533EFO_0006904, EFO_0006906
Diseaseplatelet crit

AHI1 HDAC7 NUP205 BBX CXCR4 MICB MYLK4 NAV3 TMEM131L ISG20L2 NUP160 CUX1

4.12e-0395215312EFO_0007985
Diseaseskin sensitivity to sun

OCA2 HERC2

4.31e-03191532EFO_0004795
Diseasesystolic blood pressure, alcohol drinking

CACNB2 PIK3C2A GUCY1A1 CYB561

4.51e-031281534EFO_0004329, EFO_0006335
Diseasemean arterial pressure

SH3TC2 CACNB2 GRIPAP1 FBXL13 SLCO6A1 HDAC7 GUCY1A1 CYB561

4.64e-034991538EFO_0006340
DiseaseMicrocephaly

CARS1 PQBP1 LIG4

5.14e-03671533C0025958
DiseaseGlobal developmental delay

CACNA1B PIGB TRIT1 ZNF142

5.16e-031331534C0557874

Protein segments in the cluster

PeptideGeneStartEntry
AHLKVRTAARKLIGK

UMODL1

781

Q5DID0
DHLRKDTARKLQPKS

ZNF280B

76

Q86YH2
HRRKELGKVLIDLSK

ESYT3

851

A0FGR9
HRLKNRNCKLLDSLK

CHD8

951

Q9HCK8
VKGLLDFKKRRGHSI

ATG16L2

291

Q8NAA4
SLGLKKVKGSRIHLS

CCDC116

476

Q8IYX3
GSQKRKARKTKITHL

BBX

821

Q8WY36
RLKTKENLEKTRHTL

CAVIN1

256

Q6NZI2
GHQKRKALKTTVILI

CXCR4

231

P61073
NGKRLLIHTKDSTLR

AHI1

811

Q8N157
LRKKKAANLNSIIHR

CUX1

1476

P39880
ELKKSKVLSHHRAGR

ALMS1

3691

Q8TCU4
SGKGKLTDKERHRLL

CEP55

46

Q53EZ4
LSRKLTLKAKALHAR

APOA5

231

Q6Q788
GRKDSQIKRHGKRLN

AASDH

441

Q4L235
HKGLKTLRKTEDRNS

ARAP2

1651

Q8WZ64
SEGLNRKHIPRKKRS

CCDC144CP

1151

Q8IYA2
TKHNALKDLRSQRRK

DMD

1856

P11532
ELSLSHKNNQKLRKR

CCDC87

101

Q9NVE4
NRIISKHKDLRTKGF

CAPN1

571

P07384
EKKGVLGHLKARIRA

CEP20

16

Q96NB1
RNEAKRTTKVLHGLL

CYB561

76

P49447
RLAHGVRLKANKDSL

BMS1

1136

Q14692
RLRKSGKEHIDNIKK

CAVIN4

186

Q5BKX8
SGKIHRKVKIILGRN

DBF4

571

Q9UBU7
LKRAATKKSRNDLIH

CACNA1B

416

Q00975
LAKQLVHLRKQKTRT

CHMP2B

61

Q9UQN3
NREKRGLALDGKLKH

ARRB1

281

P49407
RLIKSRGKSQAKHLN

CACNB2

406

Q08289
KRLTKRSTHAQLLRG

CECR9

181

P0C854
TDDKARHLLVLRKGN

CPT2

236

P23786
LKHQLLRVKRKVTSG

NWD2

581

Q9ULI1
RLVARALGLQHKKKE

R3HCC1

416

Q9Y3T6
RNLLKTRHKNRSPTK

RASSF9

6

O75901
GSKLSDRPLHALKRK

RAI1

1211

Q7Z5J4
RLGALHKALKKEALR

PDZRN3

176

Q9UPQ7
LQKKHRISDGILLAK

OCA2

611

Q04671
LQKSREAPGKLSRKH

PIK3C2G

366

O75747
INGKRKTAKEHLRKL

NPIPA1

136

Q9UND3
KLQRERGLGSEKHRK

NUP205

201

Q92621
KRDKQKRTALHLASA

POTEB2

131

H3BUK9
SLRNKDIKRALGIHL

OR7A5

291

Q15622
GRLLAHSKRAVKKFV

CAPN15

866

O75808
SKSHLNQLKKRRRLD

TRIT1

416

Q9H3H1
LKGKFIHTKLRKSSR

MAGI1

466

Q96QZ7
RSGKATRKKKHLEAQ

MAGEL2

881

Q9UJ55
RRKKIESLKAHANAR

NEK1

601

Q96PY6
HLKSRRLVSAKQLGV

NEMF

81

O60524
SSKRNRRHIEKKILT

NRCAM

891

Q92823
RRHIEKKILTFQGSK

NRCAM

896

Q92823
SLLKLNKKLARSVGH

NAB2

266

Q15742
LKAGRALLSHQDKLR

HERC2

2326

O95714
RLTSKRLPLKHDSKQ

LRRC53

781

A6NM62
RRTLHDKKQQLKVLS

CFAP58

781

Q5T655
KKAAEVLNKHSLSGR

HNRNPM

126

P52272
LGRTHIKDVAAKRKI

PIK3C2A

1491

O00443
SNKIKLKSRLSGGVH

PDZD2

496

O15018
LAKSGHKRLIKDLQQ

NAV3

91

Q8IVL0
ERVLKRKTFNKVLGH

GDAP1

281

Q8TB36
RHQLSKDGQKLTLLK

SLC25A22

91

Q9H936
GNAKHRNFVKKRRLL

ISG20L2

21

Q9H9L3
LHSRLNAQKKKNRGS

MYLK4

366

Q86YV6
KDAFLLKHVRRNKLG

LARP6

111

Q9BRS8
NRRKAERKKHSLKEG

ELP1

1196

O95163
GRHLKSLRNSLKTRN

ABCC2

921

Q92887
HLGKIRKRLEDVKSQ

FAM83A

6

Q86UY5
LRRTLTHIKDQKGGL

MICB

96

Q29980
INGKRKTAKEHLRKL

NPIPA3

136

F8WFD2
IINLHRSRKKIKLAG

HPSE2

501

Q8WWQ2
NGKRKTAKEHLRKLS

NPIPA2

156

E9PIF3
KRNSHIKKCTGLERI

GRM8

376

O00222
HKGLTLAALKKELRN

H1-7

71

Q75WM6
RLKSHSRDRNGLKKS

KLHL4

51

Q9C0H6
LDRIGKKNSILLHKV

HCN4

711

Q9Y3Q4
SGQHSRLKLELRKKE

PRDM9

161

Q9NQV7
ALQTRLAKRGILKHL

PQBP1

6

O60828
SKHRNERKLSVLGKD

BOD1L1

791

Q8NFC6
KGRLRNQHKVSLQKS

IGSF10

1216

Q6WRI0
HNLKKKILRFRSGSL

DACT1

816

Q9NYF0
QLRGKASGKLASKHL

LIG4

601

P49917
ARKKGRHLELANQKL

CCDC3

231

Q9BQI4
HRLKNRNCKLLEGLK

CHD6

601

Q8TD26
KRSISKRKSHLDLLK

ARFGEF3

391

Q5TH69
IVSQRKLSKSLLKHG

CPNE4

121

Q96A23
KDHLQSGRLDLSKLR

DDX50

271

Q9BQ39
GLNVLSRHKKLKELS

FBXL13

546

Q8NEE6
IGRKRKTLQLSHKSD

BRWD1

771

Q9NSI6
RIHARKLSEQRKGDK

CBR1

206

P16152
EGKTSLHKDLKQKRR

DEF6

316

Q9H4E7
RKRNRKSGKLNNHLE

MBD5

1441

Q9P267
KLKTLLKNDHIQVGR

DNAJC10

386

Q8IXB1
LRQLLHKDKSKRSAV

HDAC7

66

Q8WUI4
RSLLGSKQGHKRLIK

H1-9P

206

P60008
SEGLNRKHIPRKKRS

CCDC144A

1341

A2RUR9
KGSAALKDLKRQLHL

GRIPAP1

606

Q4V328
KCRLHLRNKGKTEEA

SCUBE3

491

Q8IX30
LDLLLTRKKRSQGLH

SCP2D1-AS1

71

Q9BR46
KSLNTQKELGLRHQK

CFAP74

226

Q9C0B2
SRTQRGGIKLHKNLL

IER5L

21

Q5T953
RNKEVKTALKTILHR

OR10D3

291

Q8NH80
LRHVEKQKSCRGLKL

JARID2

1166

Q92833
GINKRDKKKRTALHL

POTEA

91

Q6S8J7
INGKRKTAKEHLRKL

NPIPA7

136

E9PJI5
INGKRKTAKEHLRKL

NPIPA8

136

P0DM63
NRSHGKIKLRKRKST

PIGB

26

Q92521
RKTSKHKRNLAITGG

RNF19B

391

Q6ZMZ0
HKKRARRSSLLNAKK

RAPGEF6

1086

Q8TEU7
TIKDALKKHSARQLR

CARS1

416

P49589
ATAKQRLGKILKIHR

PHF2

1076

O75151
KRNVLGTTRFAHLKK

TMEM131L

556

A2VDJ0
GSILLDKDGKRKHTR

NKX6-1

226

P78426
INGKRKTAKEHLRKL

NPIPA5

136

E9PKD4
TNDLTAKRLLHVKGR

SCIN

131

Q9Y6U3
RNGRKHASVLLRKKD

IL1RAPL2

336

Q9NP60
KRDKQKRTALHLASA

POTEB

131

A0A0A6YYL3
KLLKSNRLKHLEAQG

NEPRO

396

Q6NW34
GVLHRTKTADKGKRL

ARHGAP27

501

Q6ZUM4
LFTSGIKRHLKDKRI

SGO2

11

Q562F6
GSTRIKARKRKQLHF

SLCO6A1

341

Q86UG4
KQRLRHKGSALLEKA

SH3TC2

581

Q8TF17
PNKRSKKGRLSLHRT

NAMPT

421

P43490
RPKGILKKRSNSEHR

NUAK1

396

O60285
PGLERQHSLKKSRKE

NUAK2

366

Q9H093
QGKREKLHCRKNFTL

THAP6

96

Q8TBB0
THTRALKKLSEVNKR

NFATC2IP

211

Q8NCF5
KKDLRLTAGTGHKLR

NUP160

331

Q12769
KHLESLRRKEKSGSQ

STARD8

131

Q92502
RHKKRAGQNALKFIR

SMCR8

701

Q8TEV9
KNSHKALKALLRSLV

AATF

276

Q9NY61
KGRKLRFHVLSKLLS

AATF

511

Q9NY61
RKAARLSKEALKQLH

CLSPN

276

Q9HAW4
KDKTRKRIFLHGNNL

CLVS1

241

Q8IUQ0
AGRNKSGRKHELLAK

PIAS3

26

Q9Y6X2
GLKLSKKKARRRHTD

PLEKHG5

56

O94827
HQDLVNRKARKLRKG

PDCD11

911

Q14690
NRKARKLRKGSEHQA

PDCD11

916

Q14690
KISLKLKTIGQGREH

VWDE

331

Q8N2E2
GKIFARSENLKIHKR

ZIC3

336

O60481
ELLKHNPKRRKITSN

USP22

156

Q9UPT9
RRKKGLSLHQRIKNG

ZNF182

216

P17025
KHQKKELLQRGTTTI

ZSWIM5

581

Q9P217
SAKKRRKNALIRHKS

TICRR

851

Q7Z2Z1
RTLLKKHQKIHTGER

ZSCAN31

391

Q96LW9
KSQLIHDRKCIRKLS

USP45

436

Q70EL2
KHGKEDTLRLLKNQT

TIAM2

626

Q8IVF5
AARTKRGHLVLKSFK

TMEM143

241

Q96AN5
NEHRREALKKLGLLK

SARG

586

Q9BW04
LTGVQNLRKKHKRLE

SPTAN1

1796

Q13813
LHKLVNSTRRVRKKL

SASH1

261

O94885
GIQSAKLLRHLKQKD

TBC1D30

176

Q9Y2I9
GKDLTSVLILQRKHK

SPTB

666

P11277
LGKDLIASKKLLNRH

SPTA1

821

P02549
SAVAGILKQLKRTHK

PSME4

1206

Q14997
KSNLKRHRRIHAGEK

ZNF813

311

Q6ZN06
KELRKVAHLTGKSNS

FASLG

141

P48023
KSLPLHKRNNTREKS

ZNF404

116

Q494X3
RRGHGHLTSILAKKK

UBN1

576

Q9NPG3
KQRRSKSAALLHKEL

ZZEF1

2581

O43149
RLGHKSLAQKVLRDA

TTC7A

791

Q9ULT0
RSGTKQLKHILLKDV

ZNF800

51

Q2TB10
TSKSKLKTHLLRELG

ZNF142

201

P52746
SHNLKSLRKKQLATR

WDR11

621

Q9BZH6
RGKALHQKQALRKSQ

ZNF674

201

Q2M3X9
KSFRLKRSLKAHGLQ

ZNF425

421

Q6IV72
KRSLKAHGLQHIGKR

ZNF425

426

Q6IV72
EKTFRLKGNLKSHLL

ZNF425

616

Q6IV72
HLRASTKKLTRKQGD

USP6

341

P35125
LSSGKKKHGRLIATI

TRAV41

71

A0A0B4J266
KKRLGKLKATLEQAH

GUCY1A1

426

Q02108