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 |
---|---|---|---|---|---|
C0006142 | Malignant neoplasm of breast | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C3806688 | Solute carrier family 35 member A2 congenital disorder of glycosylation | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0010324 | Crigler Najjar syndrome, type 1 | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0027651 | Neoplasms | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0010414 | Infection by Cryptococcus neoformans | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0017551 | Gilbert Disease (disorder) | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0027947 | Neutropenia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0268138 | Xeroderma Pigmentosum, Complementation Group D | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0008350 | Cholelithiasis | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0520679 | Sleep Apnea, Obstructive | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0006826 | Malignant Neoplasms | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0009402 | Colorectal Carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0014544 | Epilepsy | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0039685 | Tetralogy of Fallot | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0007097 | Carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0020433 | Hyperbilirubinemia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0677886 | Epithelial ovarian cancer | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0520680 | Sleep Apnea, Central | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C3714756 | Intellectual Disability | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C1306459 | Primary malignant neoplasm | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0279628 | Adenocarcinoma Of Esophagus | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0678222 | Breast Carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0085584 | Encephalopathies | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0002878 | Anemia, Hemolytic | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0036439 | Scoliosis, unspecified | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
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Last updated: August 19, 2024