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
Displaying entries 61651 - 61675 of 62743 in total
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