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 5101 - 5125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0206733 Strawberry nevus of skin SRD5A3 79644 steroid 5 alpha-reductase 3 Q9H8P0
C0684276 Hypsarrhythmia SRD5A3 79644 steroid 5 alpha-reductase 3 Q9H8P0
C0004352 Autistic Disorder SRD5A3 79644 steroid 5 alpha-reductase 3 Q9H8P0
C0376358 Malignant neoplasm of prostate PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0549473 Thyroid carcinoma PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0476089 Endometrial Carcinoma PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0031099 Periodontitis PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0020538 Hypertensive disease PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0151468 Thyroid Gland Follicular Adenoma PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0007103 Malignant neoplasm of endometrium PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0524620 Metabolic Syndrome X PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0011860 Diabetes Mellitus, Non-Insulin-Dependent PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0040136 Thyroid Neoplasm PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0205969 Thymic Carcinoma PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0600139 Prostate carcinoma PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0279626 Squamous cell carcinoma of esophagus PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0002395 Alzheimer's Disease PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0028754 Obesity PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0009402 Colorectal Carcinoma PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0271650 Impaired glucose tolerance PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C0001418 Adenocarcinoma PTGES2 80142 prostaglandin E synthase 2 Q9H7Z7
C1691228 Cystic Kidney Diseases ALG9 79796 ALG9 alpha-1,2-mannosyltransferase Q9H6U8
C0018798 Congenital Heart Defects ALG9 79796 ALG9 alpha-1,2-mannosyltransferase Q9H6U8
C0282577 Congenital Disorders of Glycosylation ALG9 79796 ALG9 alpha-1,2-mannosyltransferase Q9H6U8
C0016952 Galactosemias ALG9 79796 ALG9 alpha-1,2-mannosyltransferase Q9H6U8

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Last updated: August 19, 2024