| Disease ID | Disease name | Source of annotation with CYP4F22 | OMIM link | Number of associated genes | genes |
|---|---|---|---|---|---|
| PS242300 | ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE | ClinVar, OMIM, HUMSAVAR | link to OMIM | 10 | PNPLA1, ST14, ABCA12, NIPAL4, ALOXE3, LIPN, ALOX12B, CYP4F22, CERS3, TGM1 |
Download the gene annotation in CSV format
| REACTOME pathway | REACTOME ID | REACTOME IC |
|---|---|---|
| Cytochrome P450 - arranged by substrate type | R-HSA-211897 | 7.08 |
| Fatty acids | R-HSA-211935 | 9.08 |
| Biological oxidations | R-HSA-211859 | 5.55 |
| Miscellaneous substrates | R-HSA-211958 | 9.4 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 8.59 |
| Diseases of metabolism | R-HSA-5668914 | 6.57 |
| Phase 1 - Functionalization of compounds | R-HSA-211945 | 6.7 |
| Metabolism | R-HSA-1430728 | 2.34 |
| Disease | R-HSA-1643685 | 3.33 |
| Arachidonic acid metabolism | R-HSA-2142753 | 7.34 |
| Metabolism of lipids and lipoproteins | R-HSA-556833 | 3.79 |
| Eicosanoids | R-HSA-211979 | 9.4 |
| Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) | R-HSA-5579005 | 12.98 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 7.85 |
| GO term | GO ID | GO IC |
|---|---|---|
| cation binding | GO:0043169 | 1.4 |
| monooxygenase activity | GO:0004497 | 5.1 |
| transition metal ion binding | GO:0046914 | 2.48 |
| heme binding | GO:0020037 | 4.86 |
| tetrapyrrole binding | GO:0046906 | 4.8 |
| organic cyclic compound binding | GO:0097159 | 1.05 |
| oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | GO:0016705 | 4.65 |
| ion binding | GO:0043167 | 1.36 |
| catalytic activity | GO:0003824 | 1.05 |
| binding | GO:0005488 | 0.18 |
| iron ion binding | GO:0005506 | 4.65 |
| metal ion binding | GO:0046872 | 1.41 |
| heterocyclic compound binding | GO:1901363 | 1.06 |
| oxidoreductase activity | GO:0016491 | 3.12 |