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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 |
|---|---|---|---|---|---|
| C0376358 | Malignant neoplasm of prostate | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0282160 | Aplasia Cutis Congenita | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C2607914 | Allergic rhinitis (disorder) | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0035222 | Respiratory Distress Syndrome, Adult | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0345904 | Malignant neoplasm of liver | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0003850 | Arteriosclerosis | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0262655 | Recurrent urinary tract infection | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0006142 | Malignant neoplasm of breast | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0035220 | Respiratory Distress Syndrome, Newborn | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C1176475 | Ductal Carcinoma | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C1306459 | Primary malignant neoplasm | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0006826 | Malignant Neoplasms | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0600139 | Prostate carcinoma | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0007102 | Malignant tumor of colon | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C2931258 | Amaurosis congenita of Leber, type 1 | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C0011847 | Diabetes | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C1306459 | Primary malignant neoplasm | PCYT2 | 5833 | phosphate cytidylyltransferase 2, ethanolamine | Q99447 |
| C0235946 | Cerebral atrophy | PCYT2 | 5833 | phosphate cytidylyltransferase 2, ethanolamine | Q99447 |
| C0006826 | Malignant Neoplasms | PCYT2 | 5833 | phosphate cytidylyltransferase 2, ethanolamine | Q99447 |
| C0037773 | Spastic Paraplegia, Hereditary | PCYT2 | 5833 | phosphate cytidylyltransferase 2, ethanolamine | Q99447 |
| C0027651 | Neoplasms | PCYT2 | 5833 | phosphate cytidylyltransferase 2, ethanolamine | Q99447 |
| C1850598 | Leigh Syndrome due to Mitochondrial Complex III Deficiency | PDHA1 | 5160 | pyruvate dehydrogenase E1 subunit alpha 1 | P08559 |
| C0026650 | Movement Disorders | PDHA1 | 5160 | pyruvate dehydrogenase E1 subunit alpha 1 | P08559 |
| C0023264 | Leigh Disease | PDHA1 | 5160 | pyruvate dehydrogenase E1 subunit alpha 1 | P08559 |
