Toppgene analysis for Wikipedia protein communities, toppgene analysis, cc335_17, positive side

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1: GO: Molecular Function [Display Chart] 16 input genes in category / 68 annotations before applied cutoff / 18661 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 GO:0097690 iron channel inhibitor activity 8.574E-4 2.915E-2
1.400E-1
5.830E-2
1 1
2 GO:0005124 scavenger receptor binding 8.574E-4 2.915E-2
1.400E-1
5.830E-2
1 1

2: GO: Biological Process [Display Chart] 15 input genes in category / 351 annotations before applied cutoff / 18623 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 GO:0055072 iron ion homeostasis 2.984E-5 7.394E-3 4.761E-2 1.047E-2 3 77
2 GO:0015879 carnitine transport 4.699E-5 7.394E-3 4.761E-2 1.649E-2 2 13
3 GO:0015838 amino-acid betaine transport 6.320E-5 7.394E-3 4.761E-2 2.218E-2 2 15
4 GO:0055076 transition metal ion homeostasis 1.122E-4 8.009E-3
5.158E-2
3.938E-2 3 120
5 GO:0015697 quaternary ammonium group transport 1.141E-4 8.009E-3
5.158E-2
4.005E-2 2 20
6 GO:0090092 regulation of transmembrane receptor protein serine/threonine kinase signaling pathway 6.840E-4 1.885E-2
1.214E-1
2.401E-1
3 222
7 GO:0006879 cellular iron ion homeostasis 6.967E-4 1.885E-2
1.214E-1
2.445E-1
2 49
8 GO:1904254 regulation of iron channel activity 8.055E-4 1.885E-2
1.214E-1
2.827E-1
1 1
9 GO:0034760 negative regulation of iron ion transmembrane transport 8.055E-4 1.885E-2
1.214E-1
2.827E-1
1 1
10 GO:1904038 regulation of ferrous iron export 8.055E-4 1.885E-2
1.214E-1
2.827E-1
1 1
11 GO:1904255 negative regulation of iron channel activity 8.055E-4 1.885E-2
1.214E-1
2.827E-1
1 1
12 GO:0071228 cellular response to tumor cell 8.055E-4 1.885E-2
1.214E-1
2.827E-1
1 1
13 GO:1904039 negative regulation of ferrous iron export 8.055E-4 1.885E-2
1.214E-1
2.827E-1
1 1
14 GO:0034759 regulation of iron ion transmembrane transport 8.055E-4 1.885E-2
1.214E-1
2.827E-1
1 1
15 GO:0034757 negative regulation of iron ion transport 8.055E-4 1.885E-2
1.214E-1
2.827E-1
1 1
16 GO:0090287 regulation of cellular response to growth factor stimulus 1.034E-3 2.267E-2
1.460E-1
3.628E-1
3 256
17 GO:1903414 iron cation export 1.610E-3 2.975E-2
1.916E-1
5.652E-1
1 2
18 GO:0014908 myotube differentiation involved in skeletal muscle regeneration 1.610E-3 2.975E-2
1.916E-1
5.652E-1
1 2
19 GO:1903988 ferrous iron export across plasma membrane 1.610E-3 2.975E-2
1.916E-1
5.652E-1
1 2
20 GO:0030510 regulation of BMP signaling pathway 2.178E-3 3.390E-2
2.183E-1
7.643E-1
2 87
21 GO:0046916 cellular transition metal ion homeostasis 2.227E-3 3.390E-2
2.183E-1
7.817E-1
2 88
22 GO:0007178 transmembrane receptor protein serine/threonine kinase signaling pathway 2.391E-3 3.390E-2
2.183E-1
8.391E-1
3 343
23 GO:0070839 divalent metal ion export 2.415E-3 3.390E-2
2.183E-1
8.475E-1
1 3
24 GO:0034756 regulation of iron ion transport 2.415E-3 3.390E-2
2.183E-1
8.475E-1
1 3
25 GO:0044375 regulation of peroxisome size 2.415E-3 3.390E-2
2.183E-1
8.475E-1
1 3
26 GO:1903874 ferrous iron transmembrane transport 3.218E-3 4.034E-2
2.598E-1
1.000E0
1 4
27 GO:2000646 positive regulation of receptor catabolic process 3.218E-3 4.034E-2
2.598E-1
1.000E0
1 4
28 GO:1904479 negative regulation of intestinal absorption 3.218E-3 4.034E-2
2.598E-1
1.000E0
1 4
29 GO:0015696 ammonium transport 4.026E-3 4.873E-2
3.138E-1
1.000E0
2 119
Show 24 more annotations

3: GO: Cellular Component [Display Chart] 16 input genes in category / 64 annotations before applied cutoff / 19061 genes in category

No results to display

4: Human Phenotype [Display Chart] 7 input genes in category / 554 annotations before applied cutoff / 4707 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 HP:0012463 Elevated transferrin saturation 5.684E-6 3.149E-3 2.171E-2 3.149E-3 2 3
2 HP:0040135 Abnormal transferrin saturation 2.836E-5 7.856E-3
5.417E-2
1.571E-2 2 6
3 HP:0003452 Increased serum iron 1.711E-4 3.159E-2
2.178E-1
9.478E-2
2 14
4 HP:0040130 Abnormal serum iron 2.551E-4 3.534E-2
2.437E-1
1.413E-1
2 17
5 HP:0000029 Testicular atrophy 4.318E-4 4.785E-2
3.299E-1
2.392E-1
2 22

5: Mouse Phenotype [Display Chart] 12 input genes in category / 400 annotations before applied cutoff / 10355 genes in category

No results to display

6: Domain [Display Chart] 15 input genes in category / 111 annotations before applied cutoff / 18735 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 IPR027226 PIAS3 InterPro 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
2 IPR013197 RNA pol III RPC82-rel HTH InterPro 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
3 IPR033024 Neogenin InterPro 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
4 IPR002266 Connexin50 InterPro 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
5 PF06446 Hepcidin Pfam 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
6 IPR008806 RNA pol III Rpc82 C InterPro 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
7 IPR033744 RRM RBM8 InterPro 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
8 IPR010500 Hepcidin InterPro 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
9 PF05645 RNA pol Rpc82 Pfam 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
10 IPR008111 RNA-bd 8 InterPro 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
11 PF08221 HTH 9 Pfam 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
12 IPR030081 AMPK beta-2 InterPro 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
13 PF03509 Connexin50 Pfam 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
14 IPR033606 Hemojuvelin InterPro 8.006E-4 6.348E-3 3.359E-2
8.887E-2
1 1
15 IPR010560 Neogenin C InterPro 1.601E-3 7.403E-3 3.917E-2
1.777E-1
1 2
16 IPR024670 BCL9 beta-catenin-bd dom InterPro 1.601E-3 7.403E-3 3.917E-2
1.777E-1
1 2
17 PF16561 AMPK1 CBM Pfam 1.601E-3 7.403E-3 3.917E-2
1.777E-1
1 2
18 PF06583 Neogenin C Pfam 1.601E-3 7.403E-3 3.917E-2
1.777E-1
1 2
19 PF04739 AMPKBI Pfam 1.601E-3 7.403E-3 3.917E-2
1.777E-1
1 2
20 IPR032640 AMPK1 CBM InterPro 1.601E-3 7.403E-3 3.917E-2
1.777E-1
1 2
21 PF11502 BCL9 Pfam 1.601E-3 7.403E-3 3.917E-2
1.777E-1
1 2
22 SM01010 AMPKBI SMART 1.601E-3 7.403E-3 3.917E-2
1.777E-1
1 2
23 IPR006828 ASC dom InterPro 1.601E-3 7.403E-3 3.917E-2
1.777E-1
1 2
24 IPR015668 Bcl-9 InterPro 1.601E-3 7.403E-3 3.917E-2
1.777E-1
1 2
25 IPR012943 Cnn 1N InterPro 2.400E-3 8.325E-3 4.405E-2
2.664E-1
1 3
26 IPR008733 PEX11 InterPro 2.400E-3 8.325E-3 4.405E-2
2.664E-1
1 3
27 PF06535 RGM N Pfam 2.400E-3 8.325E-3 4.405E-2
2.664E-1
1 3
28 PF07989 Cnn 1N Pfam 2.400E-3 8.325E-3 4.405E-2
2.664E-1
1 3
29 IPR009496 RGM C InterPro 2.400E-3 8.325E-3 4.405E-2
2.664E-1
1 3
30 PF06534 RGM C Pfam 2.400E-3 8.325E-3 4.405E-2
2.664E-1
1 3
31 IPR010536 RGM N InterPro 2.400E-3 8.325E-3 4.405E-2
2.664E-1
1 3
32 PF05648 PEX11 Pfam 2.400E-3 8.325E-3 4.405E-2
2.664E-1
1 3
33 IPR014756 Ig E-set InterPro 3.057E-3 9.864E-3
5.219E-2
3.393E-1
2 104
34 PS51466 PINIT PROSITE 3.199E-3 9.864E-3
5.219E-2
3.551E-1
1 4
35 PF14324 PINIT Pfam 3.199E-3 9.864E-3
5.219E-2
3.551E-1
1 4
36 IPR023321 PINIT InterPro 3.199E-3 9.864E-3
5.219E-2
3.551E-1
1 4
37 PF02891 zf-MIZ Pfam 5.592E-3 1.633E-2
8.643E-2
6.207E-1
1 7
38 PS51044 ZF SP RING PROSITE 5.592E-3 1.633E-2
8.643E-2
6.207E-1
1 7
39 IPR004181 Znf MIZ InterPro 6.388E-3 1.818E-2
9.621E-2
7.091E-1
1 8
40 SM01017 Arrestin C SMART 7.980E-3 1.925E-2
1.019E-1
8.857E-1
1 10
41 PS51154 MACRO PROSITE 7.980E-3 1.925E-2
1.019E-1
8.857E-1
1 10
42 IPR011021 Arrestin-like N InterPro 7.980E-3 1.925E-2
1.019E-1
8.857E-1
1 10
43 IPR002589 Macro dom InterPro 7.980E-3 1.925E-2
1.019E-1
8.857E-1
1 10
44 PF02752 Arrestin C Pfam 7.980E-3 1.925E-2
1.019E-1
8.857E-1
1 10
45 PF00339 Arrestin N Pfam 7.980E-3 1.925E-2
1.019E-1
8.857E-1
1 10
46 IPR011022 Arrestin C-like InterPro 7.980E-3 1.925E-2
1.019E-1
8.857E-1
1 10
47 IPR000413 Integrin alpha InterPro 1.432E-2 2.893E-2
1.531E-1
1.000E0
1 18
48 PS00242 INTEGRIN ALPHA PROSITE 1.432E-2 2.893E-2
1.531E-1
1.000E0
1 18
49 PF08441 Integrin alpha2 Pfam 1.432E-2 2.893E-2
1.531E-1
1.000E0
1 18
50 IPR013649 Integrin alpha-2 InterPro 1.432E-2 2.893E-2
1.531E-1
1.000E0
1 18
Show 45 more annotations

7: Pathway [Display Chart] 14 input genes in category / 138 annotations before applied cutoff / 12450 genes in category

No results to display

8: Pubmed [Display Chart] 16 input genes in category / 1641 annotations before applied cutoff / 38193 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 11753387 Positional cloning of the combined hyperlipidemia gene Hyplip1. Pubmed 1.751E-23 2.874E-20 2.293E-19 2.874E-20 7 9
2 18326817 Hemojuvelin regulates hepcidin expression via a selective subset of BMP ligands and receptors independently of neogenin. Pubmed 1.721E-8 1.412E-5 1.127E-4 2.823E-5 3 13
3 15998830 Competitive regulation of hepcidin mRNA by soluble and cell-associated hemojuvelin. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
4 27072365 Neogenin Facilitates the Induction of Hepcidin Expression by Hemojuvelin in the Liver. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
5 22398782 Serum hemojuvelin and hepcidin levels in chronic kidney disease. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
6 23375327 Hemojuvelin and iron metabolism in kidney and heart allograft recipients. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
7 16075058 Hemojuvelin is essential for dietary iron sensing, and its mutation leads to severe iron overload. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
8 24356769 Obesity does not influence hepcidin and hemojuvelin levels in hemodialysis patients. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
9 18421430 A bone morphogenetic protein (BMP)-responsive element in the hepcidin promoter controls HFE2-mediated hepatic hepcidin expression and its response to IL-6 in cultured cells. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
10 21088809 Hemojuvelin and hepcidin gene mutations in patients with porphyria cutanea tarda from Southern France. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
11 15685557 Juvenile hemochromatosis associated with pathogenic mutations of adult hemochromatosis genes. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
12 20301349 Juvenile Hereditary Hemochromatosis Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
13 26405701 The Relationship of Serum Hemojuvelin and Hepcidin Levels with Iron Overload in Nonalcoholic Fatty Liver Disease. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
14 18445598 Neogenin-mediated hemojuvelin shedding occurs after hemojuvelin traffics to the plasma membrane. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
15 18827264 Hemojuvelin N-terminal mutants reach the plasma membrane but do not activate the hepcidin response. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
16 19564337 Hemojuvelin-neogenin interaction is required for bone morphogenic protein-4-induced hepcidin expression. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
17 19287179 Hemojuvelin: the hepcidin story continues. Pubmed 1.645E-7 1.588E-5 1.268E-4 2.700E-4 2 2
18 16103673 Iron stores modulate hepatic hepcidin expression by an HFE-independent pathway. Pubmed 4.935E-7 3.115E-5 2.486E-4 8.098E-4 2 3
19 18287331 Selective binding of RGMc/hemojuvelin, a key protein in systemic iron metabolism, to BMP-2 and neogenin. Pubmed 4.935E-7 3.115E-5 2.486E-4 8.098E-4 2 3
20 28924039 Matriptase-2 suppresses hepcidin expression by cleaving multiple components of the hepcidin induction pathway. Pubmed 4.935E-7 3.115E-5 2.486E-4 8.098E-4 2 3
21 21039223 Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload. Pubmed 4.935E-7 3.115E-5 2.486E-4 8.098E-4 2 3
22 18335997 Neogenin interacts with hemojuvelin through its two membrane-proximal fibronectin type III domains. Pubmed 4.935E-7 3.115E-5 2.486E-4 8.098E-4 2 3
23 20937842 Matriptase-2- and proprotein convertase-cleaved forms of hemojuvelin have different roles in the down-regulation of hepcidin expression. Pubmed 4.935E-7 3.115E-5 2.486E-4 8.098E-4 2 3
24 19214511 Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene. Pubmed 4.935E-7 3.115E-5 2.486E-4 8.098E-4 2 3
25 22893705 Neogenin interacts with matriptase-2 to facilitate hemojuvelin cleavage. Pubmed 4.935E-7 3.115E-5 2.486E-4 8.098E-4 2 3
26 22365732 Hepcidin is correlated to soluble hemojuvelin but not to increased GDF15 during pregnancy. Pubmed 4.935E-7 3.115E-5 2.486E-4 8.098E-4 2 3
27 27051019 BMP6 and BMP4 expression in patients with cancer-related anemia and its relationship with hepcidin and s-HJV. Pubmed 9.867E-7 5.397E-5 4.307E-4 1.619E-3 2 4
28 26633544 The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data. Pubmed 9.867E-7 5.397E-5 4.307E-4 1.619E-3 2 4
29 18762941 Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes. Pubmed 9.867E-7 5.397E-5 4.307E-4 1.619E-3 2 4
30 17942375 Gene expression of the repulsive guidance molecules/neogenin in the developing and mature mouse visual system: C57BL/6J vs. the glaucoma model DBA/2J. Pubmed 9.867E-7 5.397E-5 4.307E-4 1.619E-3 2 4
31 16032658 Gene expression of the repulsive guidance molecules during development of the mouse intestine. Pubmed 1.644E-6 8.703E-5 6.946E-4 2.698E-3 2 5
32 19787796 HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants. Pubmed 2.466E-6 1.264E-4 1.009E-3 4.046E-3 2 6
33 19252486 BMP6 is a key endogenous regulator of hepcidin expression and iron metabolism. Pubmed 5.913E-6 2.940E-4 2.347E-3 9.703E-3 2 9
34 17847004 Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance. Pubmed 9.029E-6 4.358E-4 3.478E-3 1.482E-2 2 11
35 20065295 Neogenin inhibits HJV secretion and regulates BMP-induced hepcidin expression and iron homeostasis. Pubmed 1.083E-5 5.079E-4 4.053E-3 1.778E-2 2 12
36 20801192 Hepcidin expression by human monocytes in response to adhesion and pro-inflammatory cytokines. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
37 28455998 New mutations in GJA8 expand the phenotype to include total sclerocornea. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
38 16868025 Complex biosynthesis of the muscle-enriched iron regulator RGMc. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
39 29149203 ALC1/CHD1L, a chromatin-remodeling enzyme, is required for efficient base excision repair. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
40 26055723 Regulation of Iron Metabolism by Hepcidin under Conditions of Inflammation. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
41 26174669 Mutant connexin 50 (S276F) inhibits channel and hemichannel functions inducing cataract. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
42 24283717 Deletion of thioredoxin-interacting protein preserves retinal neuronal function by preventing inflammation and vascular injury. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
43 20713458 Immunoassay for human serum hemojuvelin. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
44 11023900 Properties of gap junction channels formed by Cx46 alone and in combination with Cx50. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
45 30056060 Decreased Hepcidin Levels Are Associated with Low Steady-state Hemoglobin in Children With Sickle Cell Disease in Tanzania. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
46 18333366 IL-6 - STAT-3 - hepcidin: linking inflammation to the iron metabolism. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
47 30057485 Serum Hepcidin Level as a Marker of Iron Status in Children with Cystic Fibrosis. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
48 24954786 Hepcidin in tumor-related iron deficiency anemia and tumor-related anemia of chronic disease: pathogenic mechanisms and diagnosis. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
49 27702549 Thioredoxin interacting protein mediates lipid-induced impairment of glucose uptake in skeletal muscle. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
50 17675577 High glucose-induced thioredoxin-interacting protein in renal proximal tubule cells is independent of transforming growth factor-beta1. Pubmed 4.189E-4 1.088E-3 8.681E-3
6.875E-1
1 1
Show 45 more annotations

9: Interaction [Display Chart] 15 input genes in category / 586 annotations before applied cutoff / 17703 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 int:RGMA RGMA interactions 9.047E-5 4.491E-2
3.122E-1
5.301E-2
2 17
2 int:ZBTB32 ZBTB32 interactions 1.533E-4 4.491E-2
3.122E-1
8.983E-2
2 22
3 int:SLK SLK interactions 2.501E-4 4.885E-2
3.396E-1
1.466E-1
2 28

10: Cytoband [Display Chart] 16 input genes in category / 6 annotations before applied cutoff / 34661 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 1q21.1 1q21.1 9.683E-18 5.810E-17 1.423E-16 5.810E-17 8 83
2 1q21 1q21 8.622E-8 2.587E-7 6.337E-7 5.173E-7 4 93
3 15q22.3-q23 15q22.3-q23 1.845E-3 3.691E-3 9.042E-3 1.107E-2 1 4
4 1q12 1q12 4.607E-3 6.911E-3 1.693E-2 2.764E-2 1 10
5 9q33.2 9q33.2 1.831E-2 2.197E-2
5.383E-2
1.099E-1
1 40
6 19q13.1 19q13.1 2.509E-2 2.509E-2
6.148E-2
1.506E-1
1 55
Show 1 more annotation

11: Transcription Factor Binding Site [Display Chart] 12 input genes in category / 172 annotations before applied cutoff / 9770 genes in category

No results to display

12: Gene Family [Display Chart] 10 input genes in category / 13 annotations before applied cutoff / 18194 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 1238 Exon junction complex genenames.org 2.197E-3 1.665E-2
5.294E-2
2.856E-2 1 4
2 1311 Alpha arrestins genenames.org 3.294E-3 1.665E-2
5.294E-2
4.282E-2 1 6
3 85 Zinc fingers MIZ-type|SMC5-6 protein complex genenames.org 3.842E-3 1.665E-2
5.294E-2
4.994E-2 1 7
4 957 Peroxins genenames.org 8.762E-3 2.335E-2
7.426E-2
1.139E-1
1 16
5 1160 CD molecules|Complement system|Integrin alpha subunits genenames.org 9.852E-3 2.335E-2
7.426E-2
1.281E-1
1 18
6 314 Gap junction proteins genenames.org 1.203E-2 2.335E-2
7.426E-2
1.564E-1
1 22
7 662 Neuroblastoma breakpoint family genenames.org 1.257E-2 2.335E-2
7.426E-2
1.634E-1
1 23
8 726 RNA polymerase subunits genenames.org 1.583E-2 2.572E-2
8.180E-2
2.058E-1
1 29
Show 3 more annotations

13: Coexpression [Display Chart] 16 input genes in category / 1362 annotations before applied cutoff / 23137 genes in category

No results to display

14: Coexpression Atlas [Display Chart] 16 input genes in category / 962 annotations before applied cutoff / 21829 genes in category

No results to display

15: Computational [Display Chart] 11 input genes in category / 75 annotations before applied cutoff / 10037 genes in category

No results to display

16: MicroRNA [Display Chart] 16 input genes in category / 601 annotations before applied cutoff / 72241 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 hsa-miR-18a-5p:Functional MTI Functional MTI miRTarbase 2.550E-5 8.833E-3
6.162E-2
1.533E-2 3 262
2 hsa-miR-1225-3p:mirSVR highEffct hsa-miR-1225-3p:mirSVR nonconserved highEffect-0.5 MicroRNA.org 3.310E-5 8.833E-3
6.162E-2
1.989E-2 3 286
3 hsa-miR-4278:mirSVR highEffct hsa-miR-4278:mirSVR nonconserved highEffect-0.5 MicroRNA.org 4.409E-5 8.833E-3
6.162E-2
2.650E-2 3 315
4 hsa-miR-148b-3p:Functional MTI Functional MTI miRTarbase 9.143E-5 1.374E-2
9.584E-2
5.495E-2
3 403
5 hsa-miR-8060:Functional MTI (Weak) Functional MTI (Weak) miRTarbase 1.333E-4 1.602E-2
1.118E-1
8.009E-2
2 77
6 hsa-miR-6761-5p:Functional MTI (Weak) Functional MTI (Weak) miRTarbase 2.621E-4 2.625E-2
1.832E-1
1.575E-1
2 108
7 hsa-miR-1291:PITA hsa-miR-1291:PITA TOP PITA 3.851E-4 3.187E-2
2.223E-1
2.315E-1
2 131
8 hsa-miR-519d-5p:Functional MTI (Weak) Functional MTI (Weak) miRTarbase 4.458E-4 3.187E-2
2.223E-1
2.679E-1
2 141
9 hsa-miR-1267:PITA hsa-miR-1267:PITA TOP PITA 5.176E-4 3.187E-2
2.223E-1
3.111E-1
2 152
10 hsa-miR-518d-3p:mirSVR highEffct hsa-miR-518d-3p:mirSVR nonconserved highEffect-0.5 MicroRNA.org 7.401E-4 3.187E-2
2.223E-1
4.448E-1
2 182
11 hsa-miR-519e-5p:Functional MTI (Weak) Functional MTI (Weak) miRTarbase 7.727E-4 3.187E-2
2.223E-1
4.644E-1
2 186
12 hsa-miR-515-5p:Functional MTI (Weak) Functional MTI (Weak) miRTarbase 7.975E-4 3.187E-2
2.223E-1
4.793E-1
2 189
13 hsa-miR-556-3p:PITA hsa-miR-556-3p:PITA TOP PITA 8.059E-4 3.187E-2
2.223E-1
4.844E-1
2 190
14 hsa-miR-18a:PITA hsa-miR-18a:PITA TOP PITA 8.059E-4 3.187E-2
2.223E-1
4.844E-1
2 190
15 hsa-miR-18b:PITA hsa-miR-18b:PITA TOP PITA 8.059E-4 3.187E-2
2.223E-1
4.844E-1
2 190
16 hsa-miR-518a-3p:mirSVR highEffct hsa-miR-518a-3p:mirSVR nonconserved highEffect-0.5 MicroRNA.org 8.485E-4 3.187E-2
2.223E-1
5.099E-1
2 195
17 hsa-miR-1246:PITA hsa-miR-1246:PITA TOP PITA 1.206E-3 3.302E-2
2.304E-1
7.251E-1
2 233
18 hsa-miR-518f:mirSVR highEffct hsa-miR-518f:mirSVR nonconserved highEffect-0.5 MicroRNA.org 1.269E-3 3.302E-2
2.304E-1
7.624E-1
2 239
19 hsa-miR-6771-3p:Functional MTI (Weak) Functional MTI (Weak) miRTarbase 1.441E-3 3.302E-2
2.304E-1
8.663E-1
2 255
20 hsa-miR-455-3p:PITA hsa-miR-455-3p:PITA TOP PITA 1.453E-3 3.302E-2
2.304E-1
8.730E-1
2 256
21 hsa-miR-216b-5p:TargetScan hsa-miR-216b-5p TargetScan 1.543E-3 3.302E-2
2.304E-1
9.276E-1
2 264
22 hsa-miR-216a-5p:TargetScan hsa-miR-216a-5p TargetScan 1.578E-3 3.302E-2
2.304E-1
9.485E-1
2 267
23 hsa-miR-551b:mirSVR lowEffct hsa-miR-551b:mirSVR conserved lowEffect-0.1-0.5 MicroRNA.org 1.637E-3 3.302E-2
2.304E-1
9.838E-1
2 272
24 hsa-miR-518c:mirSVR highEffct hsa-miR-518c:mirSVR nonconserved highEffect-0.5 MicroRNA.org 1.673E-3 3.302E-2
2.304E-1
1.000E0
2 275
25 hsa-miR-551a:mirSVR lowEffct hsa-miR-551a:mirSVR conserved lowEffect-0.1-0.5 MicroRNA.org 1.782E-3 3.302E-2
2.304E-1
1.000E0
2 284
26 hsa-miR-6880-5p:Functional MTI (Weak) Functional MTI (Weak) miRTarbase 2.157E-3 3.302E-2
2.304E-1
1.000E0
2 313
27 AGCACTT,MIR-520C:MSigDB AGCACTT,MIR-520C:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
28 AGCACTT,MIR-520E:MSigDB AGCACTT,MIR-520E:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
29 AGCACTT,MIR-520D:MSigDB AGCACTT,MIR-520D:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
30 AGCACTT,MIR-302A:MSigDB AGCACTT,MIR-302A:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
31 AGCACTT,MIR-520B:MSigDB AGCACTT,MIR-520B:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
32 AGCACTT,MIR-93:MSigDB AGCACTT,MIR-93:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
33 AGCACTT,MIR-302B:MSigDB AGCACTT,MIR-302B:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
34 AGCACTT,MIR-372:MSigDB AGCACTT,MIR-372:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
35 AGCACTT,MIR-526B:MSigDB AGCACTT,MIR-526B:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
36 AGCACTT,MIR-302D:MSigDB AGCACTT,MIR-302D:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
37 AGCACTT,MIR-373:MSigDB AGCACTT,MIR-373:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
38 AGCACTT,MIR-520A:MSigDB AGCACTT,MIR-520A:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
39 AGCACTT,MIR-302C:MSigDB AGCACTT,MIR-302C:MSigDB MSigDB 2.212E-3 3.302E-2
2.304E-1
1.000E0
2 317
40 hsa-miR-125a-5p:PITA hsa-miR-125a-5p:PITA TOP PITA 2.253E-3 3.302E-2
2.304E-1
1.000E0
2 320
41 hsa-miR-125b:PITA hsa-miR-125b:PITA TOP PITA 2.253E-3 3.302E-2
2.304E-1
1.000E0
2 320
42 hsa-miR-24-2*:mirSVR highEffct hsa-miR-24-2*:mirSVR nonconserved highEffect-0.5 MicroRNA.org 2.640E-3 3.453E-2
2.409E-1
1.000E0
2 347
43 hsa-miR-551a:PITA hsa-miR-551a:PITA TOP PITA 2.655E-3 3.453E-2
2.409E-1
1.000E0
1 12
44 hsa-miR-551b:PITA hsa-miR-551b:PITA TOP PITA 2.655E-3 3.453E-2
2.409E-1
1.000E0
1 12
45 hsa-miR-518d-3p:Functional MTI (Weak) Functional MTI (Weak) miRTarbase 2.655E-3 3.453E-2
2.409E-1
1.000E0
1 12
46 hsa-miR-518a-3p:Functional MTI Functional MTI miRTarbase 2.655E-3 3.453E-2
2.409E-1
1.000E0
1 12
47 hsa-miR-183-5p:Functional MTI Functional MTI miRTarbase 2.700E-3 3.453E-2
2.409E-1
1.000E0
2 351
48 hsa-miR-5708:Functional MTI (Weak) Functional MTI (Weak) miRTarbase 2.876E-3 3.485E-2
2.432E-1
1.000E0
1 13
49 hsa-miR-216a:PITA hsa-miR-216a:PITA TOP PITA 2.884E-3 3.485E-2
2.432E-1
1.000E0
2 363
50 hsa-miR-873-5p.2:TargetScan hsa-miR-873-5p.2 TargetScan 2.900E-3 3.485E-2
2.432E-1
1.000E0
2 364
Show 45 more annotations

17: Drug [Display Chart] 16 input genes in category / 3323 annotations before applied cutoff / 22841 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 ctd:C052410 9-chloro-2-(2-furyl)-(1,2,4)triazolo(1,5-c)quinazolin-5-imine CTD 9.641E-6 2.135E-2
1.854E-1
3.204E-2 2 7
2 ctd:C433985 SU 9516 CTD 1.285E-5 2.135E-2
1.854E-1
4.270E-2 2 8
3 CID000006537 tris(2-ethylhexyl)phosphate Stitch 2.521E-5 2.792E-2
2.425E-1
8.377E-2
2 11
4 CID005365101 JH I Stitch 4.166E-5 3.461E-2
3.006E-1
1.384E-1
2 14
5 ctd:C028632 rutecarpine CTD 6.993E-5 4.647E-2
4.037E-1
2.324E-1
2 18

18: Disease [Display Chart] 14 input genes in category / 417 annotations before applied cutoff / 16205 genes in category

ID Name Source pValue FDR B&H FDR B&Y Bonferroni Genes from Input Genes in Annotation
1 C1865614 HEMOCHROMATOSIS, TYPE 2A DisGeNET Curated 6.931E-7 1.445E-4 9.554E-4 2.890E-4 2 2
2 OMIN:602390 HEMOCHROMATOSIS, TYPE 2A; HFE2A OMIM 6.931E-7 1.445E-4 9.554E-4 2.890E-4 2 2
3 C0282193 Iron Overload DisGeNET Curated 4.209E-5 5.850E-3 3.868E-2 1.755E-2 3 81
4 C0268060 Juvenile hemochromatosis DisGeNET Curated 6.270E-5 6.536E-3 4.322E-2 2.615E-2 2 14
5 C0426891 Broad thumbs DisGeNET Curated 2.587E-4 1.441E-2
9.527E-2
1.079E-1
2 28
6 C0392514 Hereditary hemochromatosis DisGeNET BeFree 6.835E-4 1.441E-2
9.527E-2
2.850E-1
3 208
7 OMIN:116200 CATARACT, ZONULAR PULVERULENT 1; CZP1 OMIM 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
8 OMIN:613313 HEMOCHROMATOSIS, TYPE 2B; HFE2B OMIM 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
9 cv:C1865616 Hemochromatosis type 2B Clinical Variations 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
10 C4025031 Aplasia/hypoplasia of the humerus DisGeNET Curated 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
11 OMIN:116150 CATARACT-MICROCORNEA SYNDROME OMIM 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
12 C4023735 Lamellar pulverulent cataract DisGeNET BeFree 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
13 cv:C1865614 Hemochromatosis type 2A Clinical Variations 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
14 cv:CN160486 Peroxisome biogenesis disorder 14B Clinical Variations 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
15 cv:C1861828 Cataract 1 Clinical Variations 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
16 C1969001 Shoulder muscle hypoplasia DisGeNET Curated 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
17 OMIN:604804 MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 3; MCPH3 OMIM 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
18 C1864153 SCHIZOPHRENIA 5 DisGeNET BeFree 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
19 OMIN:274000 CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB OMIM 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
20 cv:C0175703 Radial aplasia-thrombocytopenia syndrome Clinical Variations 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
21 cv:C1858108 Primary autosomal recessive microcephaly 3 Clinical Variations 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
22 C1865616 HEMOCHROMATOSIS, TYPE 2B DisGeNET Curated 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
23 C1858108 Microcephaly, Primary Autosomal Recessive, 3 DisGeNET Curated 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
24 C1848840 Bilateral absence of radius DisGeNET Curated 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
25 C0426900 Tibial torsion DisGeNET Curated 8.639E-4 1.441E-2
9.527E-2
3.603E-1
1 1
26 C3277059 Congenital Bilateral Cataracts DisGeNET Curated 1.272E-3 2.018E-2
1.334E-1
5.306E-1
2 62
27 C3469186 HEMOCHROMATOSIS, TYPE 1 DisGeNET Curated 1.313E-3 2.018E-2
1.334E-1
5.477E-1
2 63
28 C0002875 Cooley's anemia DisGeNET Curated 1.355E-3 2.018E-2
1.334E-1
5.651E-1
2 64
29 C0275553 Bacterial cholangitis DisGeNET BeFree 1.727E-3 2.401E-2
1.587E-1
7.202E-1
1 2
30 C4021237 Nuclear pulverulent cataract DisGeNET BeFree 1.727E-3 2.401E-2
1.587E-1
7.202E-1
1 2
31 C0018995 Hemochromatosis DisGeNET Curated 2.005E-3 2.697E-2
1.783E-1
8.360E-1
2 78
32 C1865571 Hypoplasia or unilateral/bilateral absence of ulna DisGeNET Curated 2.590E-3 3.085E-2
2.040E-1
1.000E0
1 3
33 C0272105 Anemia due to infection DisGeNET BeFree 2.590E-3 3.085E-2
2.040E-1
1.000E0
1 3
34 C1858664 HEMOCHROMATOSIS, TYPE 3 DisGeNET Curated 2.590E-3 3.085E-2
2.040E-1
1.000E0
1 3
35 C1861828 Cataract, Zonular Pulverulent 1 DisGeNET Curated 2.590E-3 3.085E-2
2.040E-1
1.000E0
1 3
36 C0009691 Congenital cataract DisGeNET Curated 3.142E-3 3.283E-2
2.170E-1
1.000E0
2 98
37 OMIN:612474 CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB OMIM 3.452E-3 3.283E-2
2.170E-1
1.000E0
1 4
38 C1860394 Multiple pancreatic cysts DisGeNET Curated 3.452E-3 3.283E-2
2.170E-1
1.000E0
1 4
39 C0149520 Acute Cholecystitis DisGeNET BeFree 3.452E-3 3.283E-2
2.170E-1
1.000E0
1 4
40 C1142276 renal anemia DisGeNET BeFree 3.452E-3 3.283E-2
2.170E-1
1.000E0
1 4
41 C0472777 Hemoglobin E/beta thalassemia disease DisGeNET Curated 3.452E-3 3.283E-2
2.170E-1
1.000E0
1 4
42 C0268059 Neonatal hemochromatosis DisGeNET BeFree 3.452E-3 3.283E-2
2.170E-1
1.000E0
1 4
43 C0239676 High forehead DisGeNET Curated 3.464E-3 3.283E-2
2.170E-1
1.000E0
2 103
44 C2677762 Tall forehead DisGeNET Curated 3.464E-3 3.283E-2
2.170E-1
1.000E0
2 103
45 C1857486 Low-set, posteriorly rotated ears DisGeNET Curated 4.081E-3 3.781E-2
2.500E-1
1.000E0
2 112
46 C0744855 hepatitis immune DisGeNET BeFree 4.313E-3 3.801E-2
2.513E-1
1.000E0
1 5
47 C0340968 Deficiency of pyruvate kinase DisGeNET Curated 4.313E-3 3.801E-2
2.513E-1
1.000E0
1 5
48 C1623038 Cirrhosis DisGeNET BeFree 4.375E-3 3.801E-2
2.513E-1
1.000E0
3 398
49 C0031154 Peritonitis DisGeNET Curated 5.055E-3 4.230E-2
2.797E-1
1.000E0
2 125
50 C1842138 Progressive hearing loss DisGeNET Curated 5.173E-3 4.230E-2
2.797E-1
1.000E0
1 6
Show 45 more annotations