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 ▼ |
---|---|---|---|---|---|
C0270763 | Familial Motor Neuron Disease | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0009714 | Hepatic Fibrosis, Congenital | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0085084 | Motor Neuron Disease | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0011570 | Mental Depression | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0037050 | Sick Building Syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C1854520 | SEBASTIAN SYNDROME | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0022735 | Klinefelter Syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0085636 | Photophobia | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0235991 | Small for gestational age (disorder) | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0339537 | Cone monochromatism | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0037772 | Spastic Paraplegia | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0002736 | Amyotrophic Lateral Sclerosis | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0030567 | Parkinson Disease | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C1857941 | Brooke-Spiegler syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0029124 | Optic Atrophy | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0342384 | Idiopathic hypogonadotropic hypogonadism | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0018916 | Hemangioma | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C4721453 | Peripheral Nervous System Diseases | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0854723 | Retinal Dystrophies | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0751495 | Seizures, Focal | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0751602 | Hereditary Autosomal Dominant Spastic Paraplegia | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C1306459 | Primary malignant neoplasm | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0014544 | Epilepsy | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0020619 | Hypogonadism | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C0007758 | Cerebellar Ataxia | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
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Last updated: August 19, 2024