Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 |
|---|---|---|---|---|---|
| C0003811 | Cardiac Arrhythmia | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0428908 | Sinus Node Dysfunction (disorder) | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0038644 | Sudden infant death syndrome | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0004238 | Atrial Fibrillation | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0015695 | Fatty Liver | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0010068 | Coronary heart disease | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0010054 | Coronary Arteriosclerosis | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0029408 | Degenerative polyarthritis | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0018801 | Heart failure | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C1168401 | Squamous cell carcinoma of the head and neck | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0037052 | Sick Sinus Syndrome | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0029422 | Osteochondrodysplasias | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0024236 | Lymphedema | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0008925 | Cleft Palate | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0020224 | Polyhydramnios | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0432194 | Schneckenbecken dysplasia | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0010417 | Cryptorchidism | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0265282 | Fibrochondrogenesis | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0013595 | Eczema | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0006142 | Malignant neoplasm of breast | COLGALT2 | 23127 | collagen beta(1-O)galactosyltransferase 2 | Q8IYK4 |
| C0002395 | Alzheimer's Disease | COLGALT2 | 23127 | collagen beta(1-O)galactosyltransferase 2 | Q8IYK4 |
| C0019159 | Hepatitis A | COLGALT2 | 23127 | collagen beta(1-O)galactosyltransferase 2 | Q8IYK4 |
| C0585442 | Osteosarcoma of bone | COLGALT2 | 23127 | collagen beta(1-O)galactosyltransferase 2 | Q8IYK4 |
| C0029410 | Osteoarthritis of hip | COLGALT2 | 23127 | collagen beta(1-O)galactosyltransferase 2 | Q8IYK4 |
| C0019158 | Hepatitis | COLGALT2 | 23127 | collagen beta(1-O)galactosyltransferase 2 | Q8IYK4 |
