Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol ▼ | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0039730 | Thalassemia | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0033860 | Psoriasis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0234533 | Generalized seizures | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0033578 | Prostatic Neoplasms | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0004096 | Asthma | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0010481 | Cushing Syndrome | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C4721555 | Autoimmune hepatitis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0241910 | Autoimmune Chronic Hepatitis | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0151744 | Myocardial Ischemia | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0020179 | Huntington Disease | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0235782 | Gallbladder Carcinoma | CYP39A1 | 51302 | cytochrome P450 family 39 subfamily A member 1 | Q9NYL5 |
| C0023530 | Leukopenia | CYP39A1 | 51302 | cytochrome P450 family 39 subfamily A member 1 | Q9NYL5 |
| C0153452 | Malignant neoplasm of gallbladder | CYP39A1 | 51302 | cytochrome P450 family 39 subfamily A member 1 | Q9NYL5 |
| C0037773 | Spastic Paraplegia, Hereditary | CYP39A1 | 51302 | cytochrome P450 family 39 subfamily A member 1 | Q9NYL5 |
| C2239176 | Liver carcinoma | CYP39A1 | 51302 | cytochrome P450 family 39 subfamily A member 1 | Q9NYL5 |
| C0376358 | Malignant neoplasm of prostate | CYP39A1 | 51302 | cytochrome P450 family 39 subfamily A member 1 | Q9NYL5 |
| C0027947 | Neutropenia | CYP39A1 | 51302 | cytochrome P450 family 39 subfamily A member 1 | Q9NYL5 |
| C0034152 | Henoch-Schoenlein Purpura | CYP2U1 | 113612 | cytochrome P450 family 2 subfamily U member 1 | Q7Z449 |
| C0037773 | Spastic Paraplegia, Hereditary | CYP2U1 | 113612 | cytochrome P450 family 2 subfamily U member 1 | Q7Z449 |
| C0524851 | Neurodegenerative Disorders | CYP2U1 | 113612 | cytochrome P450 family 2 subfamily U member 1 | Q7Z449 |
| C0037772 | Spastic Paraplegia | CYP2U1 | 113612 | cytochrome P450 family 2 subfamily U member 1 | Q7Z449 |
| C3539507 | SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE | CYP2U1 | 113612 | cytochrome P450 family 2 subfamily U member 1 | Q7Z449 |
| C0031117 | Peripheral Neuropathy | CYP2U1 | 113612 | cytochrome P450 family 2 subfamily U member 1 | Q7Z449 |
| C1306459 | Primary malignant neoplasm | CYP2U1 | 113612 | cytochrome P450 family 2 subfamily U member 1 | Q7Z449 |
| C0085131 | Gangliosidosis GM1 | CYP2U1 | 113612 | cytochrome P450 family 2 subfamily U member 1 | Q7Z449 |
