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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 |
|---|---|---|---|---|---|
| C0009806 | Constipation | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0268398 | Familial lichen amyloidosis | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C2677590 | Congenital Disorder Of Glycosylation, Type In | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0009081 | Congenital clubfoot | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0015934 | Fetal Growth Retardation | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0699885 | Carcinoma of bladder | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0017168 | Gastroesophageal reflux disease | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0005695 | Bladder Neoplasm | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0235946 | Cerebral atrophy | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0002736 | Amyotrophic Lateral Sclerosis | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C2239176 | Liver carcinoma | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0002871 | Anemia | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0858252 | Breast adenocarcinoma | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C1458155 | Mammary Neoplasms | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0017636 | Glioblastoma | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0278996 | Malignant Head and Neck Neoplasm | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0031350 | Pharyngitis | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0002395 | Alzheimer's Disease | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0020255 | Hydrocephalus | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C4721610 | Carcinoma, Ovarian Epithelial | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0027651 | Neoplasms | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0006142 | Malignant neoplasm of breast | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0038454 | Cerebrovascular accident | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0007384 | Cataplexy | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
