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 40626 - 40650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0175693 Russell-Silver syndrome AMT 275 aminomethyltransferase P48728
C0017601 Glaucoma AMT 275 aminomethyltransferase P48728
C0024299 Lymphoma AMT 275 aminomethyltransferase P48728
C0344315 Depressed mood AMT 275 aminomethyltransferase P48728
C0270855 Early myoclonic encephalopathy AMT 275 aminomethyltransferase P48728
C0008533 Hemophilia B AMT 275 aminomethyltransferase P48728
C3714756 Intellectual Disability AMT 275 aminomethyltransferase P48728
C1510586 Autism Spectrum Disorders AMT 275 aminomethyltransferase P48728
C0022336 Creutzfeldt-Jakob disease AMT 275 aminomethyltransferase P48728
C0025517 Metabolic Diseases AMT 275 aminomethyltransferase P48728
C0026769 Multiple Sclerosis AMT 275 aminomethyltransferase P48728
C1306459 Primary malignant neoplasm AMT 275 aminomethyltransferase P48728
C0006826 Malignant Neoplasms AMT 275 aminomethyltransferase P48728
C0027651 Neoplasms AMT 275 aminomethyltransferase P48728
C0085584 Encephalopathies AMT 275 aminomethyltransferase P48728
C0699889 Malignant Female Reproductive System Neoplasm AMT 275 aminomethyltransferase P48728
C0023817 Hyperlipoproteinemia Type I AMT 275 aminomethyltransferase P48728
C0011581 Depressive disorder AMT 275 aminomethyltransferase P48728
C0009402 Colorectal Carcinoma AMT 275 aminomethyltransferase P48728
C0014544 Epilepsy AMT 275 aminomethyltransferase P48728
C0220994 Hyperammonemia AMT 275 aminomethyltransferase P48728
C0010346 Crohn Disease AMT 275 aminomethyltransferase P48728
C0041296 Tuberculosis GLO1 2739 glyoxalase I Q04760
C0039101 synovial sarcoma GLO1 2739 glyoxalase I Q04760
C0011849 Diabetes Mellitus GLO1 2739 glyoxalase I Q04760

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Last updated: August 19, 2024