Reversible hydration of carbon dioxide
Pathways in the Reversible hydration of carbon dioxide SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | Reversible hydration of carbon dioxide | Reactome |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | CA5B | Carbonic Anhydrase 5B | Protein Coding | 1 |
| 2 | CA14 | Carbonic Anhydrase 14 | Protein Coding | 1 |
| 3 | CA13 | Carbonic Anhydrase 13 | Protein Coding | 1 |
| 4 | CA1 | Carbonic Anhydrase 1 | Protein Coding | 1 |
| 5 | CA2 | Carbonic Anhydrase 2 | Protein Coding | 1 |
| 6 | CA3 | Carbonic Anhydrase 3 | Protein Coding | 1 |
| 7 | CA4 | Carbonic Anhydrase 4 | Protein Coding | 1 |
| 8 | CA5A | Carbonic Anhydrase 5A | Protein Coding | 1 |
| 9 | CA6 | Carbonic Anhydrase 6 | Protein Coding | 1 |
| 10 | CA7 | Carbonic Anhydrase 7 | Protein Coding | 1 |
| 11 | CA9 | Carbonic Anhydrase 9 | Protein Coding | 1 |
| 12 | CA12 | Carbonic Anhydrase 12 | Protein Coding | 1 |
Disorders associated with Reversible hydration of carbon dioxide SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Hyperchlorhidrosis, isolated | Enrichment | CA12 | 3.05 |
| 2 | Retinitis pigmentosa 17 | Enrichment | CA4 | 3.05 |
| 3 | Carbonic anhydrase va deficiency, hyperammonemia due to | Enrichment | CA5A | 3.05 |
| 4 | Hyperammonemic encephalopathy due to carbonic anhydrase va deficiency | Enrichment | CA5A | 3.05 |
| 5 | Osteopetrosis, autosomal recessive 3 | Enrichment | CA2 | 2.75 |
| 6 | Osteopetrosis | Enrichment | CA2 | 2.35 |
| 7 | Retinitis pigmentosa | Enrichment | CA4 | 0.76 |
| 8 | Hereditary retinal dystrophy | Enrichment | CA4 | 0.64 |
| 9 | Fundus dystrophy | Enrichment | CA4 | 0.64 |
