Metalloprotease DUBs

No Pathway Network information available for Metalloprotease DUBs

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Metalloprotease DUBs SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Myeloma, multipleEnrichmentBARD1, H2AC16, H2AC173.33
2Breast cancerEnrichmentABRAXAS1, BARD1, BRCA12.96
3Endometrial cancerEnrichmentBARD1, BRCA12.83
4Palmoplantar keratoderma, punctate type iiEnrichmentBRCA12.56
5Cinca syndromeEnrichmentNLRP32.56
6Keratoendotheliitis fugax hereditariaEnrichmentNLRP32.56
7Familial cold autoinflammatory syndrome 1EnrichmentNLRP32.56
8Muckle-wells syndromeEnrichmentNLRP32.56
9Deafness, autosomal dominant 34, with or without inflammationEnrichmentNLRP32.56
10Bone marrow failure syndrome 4EnrichmentMYSM12.56
11Infant-type hemispheric gliomaEnrichmentBRCA12.56
12Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndromeEnrichmentBRCC32.56
13Congenital progressive bone marrow failure-b-cell immunodeficiency-skeletal dysplasia syndromeEnrichmentMYSM12.56
14Cryopyrin associated periodic syndromeEnrichmentNLRP32.56
15Familial amyloid nephropathy with urticaria and deafnessEnrichmentNLRP32.56
16Primary peritoneal carcinomaEnrichmentBRCA12.56
17Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism, and facial dysmorphismEnrichmentBRCC32.26
18Fanconi anemia, complementation group sEnrichmentBRCA12.26
19Menke-hennekam syndrome 2EnrichmentEP3002.26
20Pancreatic cancer 4EnrichmentBRCA12.26
21Pericardial effusionEnrichmentNLRP32.26
22Microcephaly-capillary malformation syndromeEnrichmentSTAMBP2.26
23Inflammatory breast carcinomaEnrichmentBRCA12.26
24Peritoneum cancerEnrichmentBRCA12.26
25Bilateral breast cancerEnrichmentBRCA12.26
26Submucosal cleft palateEnrichmentUBB2.26
27Cleft hard palateEnrichmentUBB2.26
28Inherited cancer-predisposing syndromeEnrichmentABRAXAS1, BARD1, BRCA12.26
29Gastric cancerEnrichmentBARD1, BRCA12.22
30Hereditary breast carcinomaEnrichmentBARD1, BRCA12.20
31Uvula, bifidEnrichmentUBB2.09
32Cleft soft palateEnrichmentUBB2.09
33Hereditary breast ovarian cancer syndromeEnrichmentBARD1, BRCA12.01
34Polyposis syndrome, hereditary mixed, 1EnrichmentBRCA11.96
35CholangiocarcinomaEnrichmentBRCA11.96
36Breast-ovarian cancer, familial 2EnrichmentBRCA11.87
37Rubinstein-taybi syndrome 2EnrichmentEP3001.87
38Rubinstein-taybi syndrome 1EnrichmentEP3001.79
39Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.79
40Colorectal cancerEnrichmentBRCA1, EP3001.63
41Charge syndromeEnrichmentEP3001.61
42Uterine corpus cancerEnrichmentBRCA11.53
43Ovarian cancerEnrichmentBARD1, BRCA11.51
44Breast-ovarian cancer, familial 1EnrichmentBRCA11.46
45Periventricular nodular heterotopiaEnrichmentBRCA11.43
46Polydactyly, postaxial, type a1EnrichmentEP3001.40
47Rare genetic intellectual disabilityEnrichmentEP3001.40
48RhabdomyosarcomaEnrichmentBRCA11.37
49Arteriovenous malformations of the brainEnrichmentNLRP31.30
50HepatoblastomaEnrichmentBARD11.25
51Autoinflammatory diseaseEnrichmentNLRP31.20
52Pancreatic cancerEnrichmentBRCA11.18
53Bladder cancerEnrichmentBRCA11.12
54Prostate cancerEnrichmentBRCA11.12
55Lung cancerEnrichmentBRCA11.08
56Fanconi anemia, complementation group aEnrichmentBRCA11.04
57MicrocephalyEnrichmentEP3000.54

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