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 ▲ |
|---|---|---|---|---|---|
| C2936791 | Antley-Bixler Syndrome, Autosomal Dominant | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0015624 | Fanconi Syndrome | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0153252 | Systemic candidiasis | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0027651 | Neoplasms | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0300934 | Primary Amebic Meningoencephalitis | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C2239176 | Liver carcinoma | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0154251 | Lipid Metabolism Disorders | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0268151 | Classical galactosemia | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C2931826 | Potassium aggravated myotonia | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0023903 | Liver neoplasms | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C2931187 | Nephropathic cystinosis | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0033740 | Protozoan Infections | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0423775 | Scurfiness of scalp | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0086543 | Cataract | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0221244 | Seborrheic dermatitis of scalp | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0887833 | Carcinoma, Pancreatic Ductal | UGP2 | 7360 | UDP-glucose pyrophosphorylase 2 | Q16851 |
| C0007131 | Non-Small Cell Lung Carcinoma | UGP2 | 7360 | UDP-glucose pyrophosphorylase 2 | Q16851 |
| C0027651 | Neoplasms | UGP2 | 7360 | UDP-glucose pyrophosphorylase 2 | Q16851 |
| C4551506 | Paroxysmal Nonkinesigenic Dyskinesia 1 | UGP2 | 7360 | UDP-glucose pyrophosphorylase 2 | Q16851 |
| C0268151 | Classical galactosemia | UGP2 | 7360 | UDP-glucose pyrophosphorylase 2 | Q16851 |
| C2239176 | Liver carcinoma | UGP2 | 7360 | UDP-glucose pyrophosphorylase 2 | Q16851 |
| C0017638 | Glioma | UGP2 | 7360 | UDP-glucose pyrophosphorylase 2 | Q16851 |
| C0016952 | Galactosemias | UGP2 | 7360 | UDP-glucose pyrophosphorylase 2 | Q16851 |
| C0017636 | Glioblastoma | UGP2 | 7360 | UDP-glucose pyrophosphorylase 2 | Q16851 |
| C0235974 | Pancreatic carcinoma | UGP2 | 7360 | UDP-glucose pyrophosphorylase 2 | Q16851 |
