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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 ▼ |
|---|---|---|---|---|---|
| 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 |
| C0020505 | Hyperphagia | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0234533 | Generalized seizures | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0010495 | Cutis Laxa | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0023895 | Liver diseases | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C1842836 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0025958 | Microcephaly | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0005695 | Bladder Neoplasm | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C3714756 | Intellectual Disability | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0038273 | Stereotypic Movement Disorder | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
| C0013384 | Dyskinetic syndrome | MAN1B1 | 11253 | mannosidase alpha class 1B member 1 | Q9UKM7 |
