FTO obesity variant mechanism
Pathways in the FTO obesity variant mechanism SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | FTO obesity variant mechanism | WikiPathways |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | ARID5B | AT-Rich Interaction Domain 5B | Protein Coding | 1 |
| 2 | IRX3 | Iroquois Homeobox 3 | Protein Coding | 1 |
| 3 | FTO | FTO Alpha-Ketoglutarate Dependent Dioxygenase | Protein Coding | 1 |
| 4 | UCP1 | Uncoupling Protein 1 | Protein Coding | 1 |
| 5 | TBX1 | T-Box Transcription Factor 1 | Protein Coding | 1 |
| 6 | PRDM16 | PR/SET Domain 16 | Protein Coding | 1 |
| 7 | PPARGC1A | PPARG Coactivator 1 Alpha | Protein Coding | 1 |
| 8 | IRX5 | Iroquois Homeobox 5 | Protein Coding | 1 |
Disorders associated with FTO obesity variant mechanism SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Velocardiofacial syndrome | Enrichment | TBX1 | 3.23 |
| 2 | Left ventricular noncompaction 8 | Enrichment | PRDM16 | 3.23 |
| 3 | Growth retardation, developmental delay, and facial dysmorphism | Enrichment | FTO | 3.23 |
| 4 | Body mass index quantitative trait locus 14 | Enrichment | FTO | 3.23 |
| 5 | Chromosome 22q11.2 duplication syndrome | Enrichment | TBX1 | 2.93 |
| 6 | Hamamy syndrome | Enrichment | IRX5 | 2.93 |
| 7 | Craniofacial dysplasia - osteopenia syndrome | Enrichment | IRX5 | 2.93 |
| 8 | Kbg syndrome | Enrichment | TBX1 | 2.53 |
| 9 | Persistent truncus arteriosus | Enrichment | TBX1 | 2.53 |
| 10 | Conotruncal heart malformations | Enrichment | TBX1 | 2.45 |
| 11 | Digeorge syndrome | Enrichment | TBX1 | 2.15 |
| 12 | Chromosome 1p36 deletion syndrome | Enrichment | PRDM16 | 2.12 |
| 13 | Tetralogy of fallot | Enrichment | TBX1 | 1.82 |
| 14 | Left ventricular noncompaction | Enrichment | PRDM16 | 1.69 |
| 15 | Body mass index quantitative trait locus 11 | Enrichment | FTO | 1.54 |
| 16 | Familial isolated dilated cardiomyopathy | Enrichment | PRDM16 | 1.51 |
| 17 | Frontotemporal dementia and/or amyotrophic lateral sclerosis 7 | Enrichment | PPARGC1A | 1.47 |