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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 |
|---|---|---|---|---|---|
| C0023418 | leukemia | FMOD | 2331 | fibromodulin | Q06828 |
| C0021364 | Male infertility | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0036337 | Schizoaffective Disorder | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0027651 | Neoplasms | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0376545 | Hematologic Neoplasms | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0036341 | Schizophrenia | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0025322 | Premature Menopause | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0027051 | Myocardial Infarction | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C3463824 | MYELODYSPLASTIC SYNDROME | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0029408 | Degenerative polyarthritis | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0032463 | Polycythemia Vera | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0085215 | Ovarian Failure, Premature | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0004936 | Mental disorders | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0236733 | Amphetamine-Related Disorders | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0002395 | Alzheimer's Disease | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0742343 | Acute Chest Syndrome | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0018802 | Congestive heart failure | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
| C0796012 | Krause-Kivlin syndrome | POFUT2 | 23275 | protein O-fucosyltransferase 2 | Q9Y2G5 |
| C0036341 | Schizophrenia | POFUT2 | 23275 | protein O-fucosyltransferase 2 | Q9Y2G5 |
| C0024530 | Malaria | POFUT2 | 23275 | protein O-fucosyltransferase 2 | Q9Y2G5 |
| C0282577 | Congenital Disorders of Glycosylation | POFUT2 | 23275 | protein O-fucosyltransferase 2 | Q9Y2G5 |
| C0265259 | Popliteal pterygium syndrome | POFUT2 | 23275 | protein O-fucosyltransferase 2 | Q9Y2G5 |
| C0026769 | Multiple Sclerosis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0004364 | Autoimmune Diseases | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0020538 | Hypertensive disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
