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 |
---|---|---|---|---|---|
C0600139 | Prostate carcinoma | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0027651 | Neoplasms | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0338508 | Optic Atrophy 1 | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0162830 | Dermatitis, Phototoxic | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0024530 | Malaria | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0338451 | Frontotemporal dementia | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0007134 | Renal Cell Carcinoma | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0699790 | Colon Carcinoma | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C1527358 | Phototoxicity | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0038454 | Cerebrovascular accident | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C0038220 | Status Epilepticus | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
C3553571 | Carbohydrate deficient glycoprotein syndrome type 2k | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0575158 | Kyphoscoliosis deformity of spine | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0241005 | Creatine phosphokinase serum increased | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0011989 | Camurati-Engelmann Syndrome | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C1306459 | Primary malignant neoplasm | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0002452 | Amelogenesis Imperfecta | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C2239176 | Liver carcinoma | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0013336 | Dwarfism | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0000768 | Congenital Abnormality | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0027859 | Acoustic Neuroma | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0282577 | Congenital Disorders of Glycosylation | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0029456 | Osteoporosis | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0392476 | Epiphyseal dysplasia | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
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Last updated: August 19, 2024