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 60976 - 61000 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0015695 Fatty Liver ACLY 47 ATP citrate lyase P53396
C0409959 Osteoarthritis, Knee ACLY 47 ATP citrate lyase P53396
C0024115 Lung diseases ACLY 47 ATP citrate lyase P53396
C0018790 Cardiac Arrest ACLY 47 ATP citrate lyase P53396
C0018802 Congestive heart failure ACLY 47 ATP citrate lyase P53396
C0162871 Aortic Aneurysm, Abdominal ACLY 47 ATP citrate lyase P53396
C0040997 Trigeminal Neuralgia ACLY 47 ATP citrate lyase P53396
C0003864 Arthritis ACLY 47 ATP citrate lyase P53396
C0677886 Epithelial ovarian cancer ACLY 47 ATP citrate lyase P53396
C1561643 Chronic Kidney Diseases ACLY 47 ATP citrate lyase P53396
C0024121 Lung Neoplasms ACLY 47 ATP citrate lyase P53396
C0007131 Non-Small Cell Lung Carcinoma ACLY 47 ATP citrate lyase P53396
C0003869 Arthritis, Infectious ACLY 47 ATP citrate lyase P53396
C0028945 oligodendroglioma ACLY 47 ATP citrate lyase P53396
C0024623 Malignant neoplasm of stomach ACLY 47 ATP citrate lyase P53396
C0018801 Heart failure ACLY 47 ATP citrate lyase P53396
C0751713 Inclusion Body Myopathy, Sporadic ACLY 47 ATP citrate lyase P53396
C2239176 Liver carcinoma ACLY 47 ATP citrate lyase P53396
C0020473 Hyperlipidemia ACLY 47 ATP citrate lyase P53396
C0235527 Heart Failure, Right-Sided ACLY 47 ATP citrate lyase P53396
C0015302 External exotoses ACLY 47 ATP citrate lyase P53396
C0751383 Juvenile Neuronal Ceroid Lipofuscinosis ACLY 47 ATP citrate lyase P53396
C0039103 Synovitis ACLY 47 ATP citrate lyase P53396
C0023467 Leukemia, Myelocytic, Acute ACLY 47 ATP citrate lyase P53396
C0002395 Alzheimer's Disease ACHE 43 acetylcholinesterase (Cartwright blood group) P22303

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Last updated: August 19, 2024