FOXP3 in COVID-19
Pathways in the FOXP3 in COVID-19 SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | FOXP3 in COVID-19 | WikiPathways |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | CD86 | CD86 Molecule | Protein Coding | 1 |
| 2 | CD80 | CD80 Molecule | Protein Coding | 1 |
| 3 | CD28 | CD28 Molecule | Protein Coding | 1 |
| 4 | STAT5B | Signal Transducer And Activator Of Transcription 5B | Protein Coding | 1 |
| 5 | STAT5A | Signal Transducer And Activator Of Transcription 5A | Protein Coding | 1 |
| 6 | FOXP3 | Forkhead Box P3~Name Same As:- HGNC:13781 | Protein Coding | 1 |
Disorders associated with FOXP3 in COVID-19 SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Immunodysregulation, polyendocrinopathy, and enteropathy, x-linked | Enrichment | FOXP3 | 3.35 |
| 2 | Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant | Enrichment | STAT5B | 3.35 |
| 3 | Immunodeficiency 123 with hpv-related verrucosis | Enrichment | CD28 | 3.35 |
| 4 | Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly | Enrichment | FOXP3 | 3.05 |
| 5 | Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessive | Enrichment | STAT5B | 3.05 |
| 6 | Laron syndrome with immunodeficiency | Enrichment | STAT5B | 3.05 |
| 7 | Mycosis fungoides | Enrichment | CD28 | 2.88 |
| 8 | Saczary syndrome | Enrichment | CD28 | 2.88 |
| 9 | Type 1 diabetes mellitus | Enrichment | FOXP3 | 2.58 |
| 10 | Hydrops fetalis | Enrichment | FOXP3 | 2.40 |
| 11 | Acute promyelocytic leukemia | Enrichment | STAT5B | 2.24 |
| 12 | Centronuclear myopathy | Enrichment | FOXP3 | 2.03 |