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 52801 - 52825 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C2711227 Steatohepatitis ACSL5 51703 acyl-CoA synthetase long chain family member 5 Q9ULC5
C0006142 Malignant neoplasm of breast ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0600139 Prostate carcinoma ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0027651 Neoplasms ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0400966 Non-alcoholic Fatty Liver Disease ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0041696 Unipolar Depression ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0034194 Pyloric Stenosis ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0023269 leiomyosarcoma ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C1306459 Primary malignant neoplasm ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0033687 Proteinuria ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0009402 Colorectal Carcinoma ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0036341 Schizophrenia ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C3714756 Intellectual Disability ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0268731 Renal glomerular disease ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C1136249 Mental Retardation, X-Linked ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0016202 Flatfoot ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0011570 Mental Depression ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C2239176 Liver carcinoma ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0038379 Strabismus ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0027868 Neuromuscular Diseases ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0027092 Myopia ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C1261473 Sarcoma ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C1845672 Mental Retardation, X-Linked 63 ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0235991 Small for gestational age (disorder) ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0699791 Stomach Carcinoma ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488

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Last updated: August 19, 2024