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 56951 - 56975 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0035222 Respiratory Distress Syndrome, Adult SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0022283 Incontinentia Pigmenti Achromians SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0524620 Metabolic Syndrome X SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C1332206 Adult Lymphoma SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0006267 Bronchiectasis SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0340076 Asthmatic pulmonary eosinophilia SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0023890 Liver Cirrhosis SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C1306459 Primary malignant neoplasm SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0751606 Adult Acute Lymphocytic Leukemia SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0034068 Pulmonary Eosinophilia SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0162309 Adrenoleukodystrophy SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0023467 Leukemia, Myelocytic, Acute SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C1850900 Familial primary gastric lymphoma SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0028754 Obesity SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0162557 Liver Failure, Acute SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0023452 Childhood Acute Lymphoblastic Leukemia SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0279626 Squamous cell carcinoma of esophagus SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0023449 Acute lymphocytic leukemia SLC27A5 10998 solute carrier family 27 member 5 Q9Y2P5
C0010691 Cystinuria SLC3A1 6519 solute carrier family 3 member 1 Q07837
C1848030 Hypotonia-Cystinuria Syndrome SLC3A1 6519 solute carrier family 3 member 1 Q07837
C0022661 Kidney Failure, Chronic SLC3A1 6519 solute carrier family 3 member 1 Q07837
C0017636 Glioblastoma SLC3A1 6519 solute carrier family 3 member 1 Q07837
C1621958 Glioblastoma Multiforme SLC3A1 6519 solute carrier family 3 member 1 Q07837
C1857388 Cystinuria, Type A SLC3A1 6519 solute carrier family 3 member 1 Q07837
C0027709 Nephrocalcinosis SLC3A1 6519 solute carrier family 3 member 1 Q07837

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Last updated: August 19, 2024