Deregulation of Rab and Rab effector genes in bladder cancer
No Pathway Network information available for Deregulation of Rab and Rab effector genes in bladder cancer
Pathways in the Deregulation of Rab and Rab effector genes in bladder cancer SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | Deregulation of Rab and Rab effector genes in bladder cancer | WikiPathways |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | RPH3AL | Rabphilin 3A Like (Without C2 Domains) | Protein Coding | 1 |
| 2 | MLPH | Melanophilin | Protein Coding | 1 |
| 3 | RAB27B | RAB27B, Member RAS Oncogene Family | Protein Coding | 1 |
| 4 | RAB27A | RAB27A, Member RAS Oncogene Family | Protein Coding | 1 |
| 5 | EXPH5 | Exophilin 5 | Protein Coding | 1 |
| 6 | UNC13D | Unc-13 Homolog D | Protein Coding | 1 |
| 7 | GCC2 | GRIP And Coiled-Coil Domain Containing 2 | Protein Coding | 1 |
| 8 | SYTL5 | Synaptotagmin Like 5 | Protein Coding | 1 |
| 9 | SYTL4 | Synaptotagmin Like 4 | Protein Coding | 1 |
| 10 | SYTL3 | Synaptotagmin Like 3 | Protein Coding | 1 |
| 11 | MADD | MAP Kinase Activating Death Domain | Protein Coding | 1 |
| 12 | SYTL1 | Synaptotagmin Like 1 | Protein Coding | 1 |
| 13 | TBC1D10A | TBC1 Domain Family Member 10A | Protein Coding | 1 |
| 14 | SYTL2 | Synaptotagmin Like 2 | Protein Coding | 1 |
| 15 | MYRIP | Myosin VIIA And Rab Interacting Protein | Protein Coding | 1 |
| 16 | RPH3A | Rabphilin 3A | Protein Coding | 1 |
Disorders associated with Deregulation of Rab and Rab effector genes in bladder cancer SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Autoinflammatory disease | Enrichment | RAB27A, UNC13D | 3.45 |
| 2 | Griscelli syndrome, type 2 | Enrichment | RAB27A | 2.93 |
| 3 | Deeah syndrome | Enrichment | MADD | 2.93 |
| 4 | Epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive | Enrichment | EXPH5 | 2.93 |
| 5 | Neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia | Enrichment | MADD | 2.93 |
| 6 | Griscelli syndrome | Enrichment | RAB27A | 2.93 |
| 7 | Griscelli syndrome, type 3 | Enrichment | MLPH | 2.63 |
| 8 | Hemophagocytic lymphohistiocytosis, familial, 3 | Enrichment | UNC13D | 2.63 |
| 9 | Hemophagocytic lymphohistiocytosis, familial, 1 | Enrichment | UNC13D | 2.23 |
| 10 | Multiple acyl-coa dehydrogenase deficiency, severe neonatal type | Enrichment | MADD | 2.23 |
| 11 | Multisystem inflammatory syndrome in children | Enrichment | RAB27A | 1.59 |
| 12 | Complex neurodevelopmental disorder | Enrichment | MADD | 0.86 |