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 |
---|---|---|---|---|---|
C0085136 | Central Nervous System Neoplasms | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
C0004352 | Autistic Disorder | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
C0029422 | Osteochondrodysplasias | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
C0282577 | Congenital Disorders of Glycosylation | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
C1510586 | Autism Spectrum Disorders | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
C0017638 | Glioma | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
C0036857 | Severe intellectual disability | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
C0014544 | Epilepsy | SLC35A3 | 23443 | solute carrier family 35 member A3 | Q9Y2D2 |
C1857276 | Trichohepatoenteric Syndrome | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0011991 | Diarrhea | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0023530 | Leukopenia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0699790 | Colon Carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0007102 | Malignant tumor of colon | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
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 |
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Last updated: August 19, 2024