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 |
|---|---|---|---|---|---|
| C0005587 | Depression, Bipolar | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C4282128 | PATENT DUCTUS ARTERIOSUS 1 | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C3714756 | Intellectual Disability | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C1531647 | Cerebral ventriculomegaly | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0009404 | Colorectal Neoplasms | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0005586 | Bipolar Disorder | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0392525 | Nephrolithiasis | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0038454 | Cerebrovascular accident | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0036572 | Seizures | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0025958 | Microcephaly | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0024713 | Manic Disorder | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0338831 | Manic | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0026650 | Movement Disorders | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0017168 | Gastroesophageal reflux disease | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C0004352 | Autistic Disorder | NTNG1 | 22854 | netrin G1 | Q9Y2I2 |
| C4317224 | Congenital disorder of glycosylation type 1q | DOLK | 22845 | dolichol kinase | Q9UPQ8 |
| C0023787 | Lipodystrophy | DOLK | 22845 | dolichol kinase | Q9UPQ8 |
| C1835849 | Congenital Disorder Of Glycosylation, Type Im | DOLK | 22845 | dolichol kinase | Q9UPQ8 |
| C0020757 | Ichthyoses | DOLK | 22845 | dolichol kinase | Q9UPQ8 |
| C0000768 | Congenital Abnormality | DOLK | 22845 | dolichol kinase | Q9UPQ8 |
| C0007193 | Cardiomyopathy, Dilated | DOLK | 22845 | dolichol kinase | Q9UPQ8 |
| C0009714 | Hepatic Fibrosis, Congenital | DOLK | 22845 | dolichol kinase | Q9UPQ8 |
| C0241005 | Creatine phosphokinase serum increased | DOLK | 22845 | dolichol kinase | Q9UPQ8 |
| C4551675 | Keratoderma, Palmoplantar | DOLK | 22845 | dolichol kinase | Q9UPQ8 |
| C0340427 | Familial dilated cardiomyopathy | DOLK | 22845 | dolichol kinase | Q9UPQ8 |
