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 |
---|---|---|---|---|---|
C0238339 | Hereditary pancreatitis | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0949541 | Hurthle Cell Tumor | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0008370 | Cholestasis | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0206695 | Carcinoma, Neuroendocrine | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0007112 | Adenocarcinoma of prostate | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0346255 | Oncocytoma, renal | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0027819 | Neuroblastoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0027888 | Hereditary Motor and Sensory Neuropathies | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0028754 | Obesity | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0043395 | Yellow Fever | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C2937421 | Prostatic Hyperplasia | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0018801 | Heart failure | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0020179 | Huntington Disease | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0684249 | Carcinoma of lung | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0005398 | Cholestasis, Extrahepatic | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C2239176 | Liver carcinoma | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0016667 | Fragile X Syndrome | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0812413 | Malignant Pleural Mesothelioma | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C1332986 | Childhood Osteosarcoma | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C3463824 | MYELODYSPLASTIC SYNDROME | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0022336 | Creutzfeldt-Jakob disease | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0007847 | Malignant tumor of cervix | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C1306459 | Primary malignant neoplasm | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0029456 | Osteoporosis | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C1621958 | Glioblastoma Multiforme | ALPP | 250 | alkaline phosphatase, placental | P05187 |
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Last updated: August 19, 2024