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 54101 - 54125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0015930 Fetal Distress ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0020224 Polyhydramnios ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0020676 Hypothyroidism ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C3887499 Renal cyst ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0040034 Thrombocytopenia ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0158683 Polycystic liver disease ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0002871 Anemia ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0021831 Intestinal Diseases ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0013274 Patent ductus arteriosus ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0033680 Protein-Losing Enteropathies ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0008370 Cholestasis ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C1691228 Cystic Kidney Diseases ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0024236 Lymphedema ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0011581 Depressive disorder ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0009081 Congenital clubfoot ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0018816 Heart Septal Defects ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0086543 Cataract ALG8 79053 ALG8 alpha-1,3-glucosyltransferase Q9BVK2
C0005586 Bipolar Disorder POGLUT2 79070 protein O-glucosyltransferase 2 Q6UW63
C1847540 Azoospermia, Nonobstructive ELOVL6 79071 ELOVL fatty acid elongase 6 Q9H5J4
C0033860 Psoriasis ELOVL6 79071 ELOVL fatty acid elongase 6 Q9H5J4
C0027651 Neoplasms ELOVL6 79071 ELOVL fatty acid elongase 6 Q9H5J4
C0011860 Diabetes Mellitus, Non-Insulin-Dependent ELOVL6 79071 ELOVL fatty acid elongase 6 Q9H5J4
C1800706 Idiopathic Pulmonary Fibrosis ELOVL6 79071 ELOVL fatty acid elongase 6 Q9H5J4
C1704272 Benign Prostatic Hyperplasia ELOVL6 79071 ELOVL fatty acid elongase 6 Q9H5J4
C2239176 Liver carcinoma ELOVL6 79071 ELOVL fatty acid elongase 6 Q9H5J4

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