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 15476 - 15500 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0684249 Carcinoma of lung LPIN1 23175 lipin 1 Q14693
C0162309 Adrenoleukodystrophy LPIN1 23175 lipin 1 Q14693
C0242379 Malignant neoplasm of lung LPIN1 23175 lipin 1 Q14693
C0887850 Polycystic Kidney, Type 1 Autosomal Dominant Disease GANAB 23193 glucosidase II alpha subunit Q14697
C0085413 Polycystic Kidney, Autosomal Dominant GANAB 23193 glucosidase II alpha subunit Q14697
C3887964 POLYCYSTIC KIDNEY DISEASE 3 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE GANAB 23193 glucosidase II alpha subunit Q14697
C0026769 Multiple Sclerosis GANAB 23193 glucosidase II alpha subunit Q14697
C0014070 Encephalomyelitis GANAB 23193 glucosidase II alpha subunit Q14697
C0029408 Degenerative polyarthritis GANAB 23193 glucosidase II alpha subunit Q14697
C0158683 Polycystic liver disease GANAB 23193 glucosidase II alpha subunit Q14697
C0023895 Liver diseases GANAB 23193 glucosidase II alpha subunit Q14697
C0022680 Polycystic Kidney Diseases GANAB 23193 glucosidase II alpha subunit Q14697
C2751306 Polycystic kidney disease, type 2 GANAB 23193 glucosidase II alpha subunit Q14697
C0022104 Irritable Bowel Syndrome ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C0220597 Adult Hodgkin Lymphoma ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C0678222 Breast Carcinoma ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C0024291 Lymphohistiocytosis, Hemophagocytic ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C0023434 Chronic Lymphocytic Leukemia ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C0162309 Adrenoleukodystrophy ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C3160718 PARKINSON DISEASE, LATE-ONSET ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C0026764 Multiple Myeloma ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C0024299 Lymphoma ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C0020179 Huntington Disease ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C0021051 Immunologic Deficiency Syndromes ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2
C1306459 Primary malignant neoplasm ACSBG1 23205 acyl-CoA synthetase bubblegum family member 1 Q96GR2

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Last updated: August 19, 2024