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 15626 - 15650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0751396 Well Differentiated Oligodendroglioma PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0017636 Glioblastoma PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0014175 Endometriosis PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0004114 Astrocytoma PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0027819 Neuroblastoma PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0007102 Malignant tumor of colon PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0037369 Smoking PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0014544 Epilepsy PLCB1 23236 phospholipase C beta 1 Q9NQ66
C1868684 EAR, PATELLA, SHORT STATURE SYNDROME PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0005586 Bipolar Disorder PLCB1 23236 phospholipase C beta 1 Q9NQ66
C1858723 Poikiloderma with Neutropenia PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0751495 Seizures, Focal PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0027051 Myocardial Infarction PLCB1 23236 phospholipase C beta 1 Q9NQ66
C2239176 Liver carcinoma PLCB1 23236 phospholipase C beta 1 Q9NQ66
C4552072 X-linked infantile spasms PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0027126 Myotonic Dystrophy PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0007222 Cardiovascular Diseases PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0008312 Primary biliary cirrhosis PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0338106 Adenocarcinoma of colon PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0026691 Mucocutaneous Lymph Node Syndrome PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0700095 Central neuroblastoma PLCB1 23236 phospholipase C beta 1 Q9NQ66
C0009375 Colonic Neoplasms PLCB1 23236 phospholipase C beta 1 Q9NQ66
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

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Last updated: August 19, 2024