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 57201 - 57225 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0006826 Malignant Neoplasms AMY1A 276 amylase alpha 1A P04745
C0003469 Anxiety Disorders AMY1A 276 amylase alpha 1A P04745
C0036341 Schizophrenia AMY1A 276 amylase alpha 1A P04745
C0085159 Seasonal Affective Disorder AMY1A 276 amylase alpha 1A P04745
C1527336 Sjogren's Syndrome AMY1A 276 amylase alpha 1A P04745
C2239176 Liver carcinoma AMY1A 276 amylase alpha 1A P04745
C0020538 Hypertensive disease AMY1A 276 amylase alpha 1A P04745
C0086132 Depressive Symptoms AMY1A 276 amylase alpha 1A P04745
C1269683 Major Depressive Disorder AMY1A 276 amylase alpha 1A P04745
C0020459 Hyperinsulinism AMY1A 276 amylase alpha 1A P04745
C0270549 Generalized Anxiety Disorder AMY1A 276 amylase alpha 1A P04745
C2607914 Allergic rhinitis (disorder) AMY1A 276 amylase alpha 1A P04745
C0152013 Adenocarcinoma of lung (disorder) AMY1A 276 amylase alpha 1A P04745
C0751748 Nonketotic Hyperglycinemia AMT 275 aminomethyltransferase P48728
C0036572 Seizures AMT 275 aminomethyltransferase P48728
C0010043 Corneal Ulcer AMT 275 aminomethyltransferase P48728
C0030305 Pancreatitis AMT 275 aminomethyltransferase P48728
C0027066 Myoclonus AMT 275 aminomethyltransferase P48728
C0795830 CHROMOSOME 9p DELETION SYNDROME AMT 275 aminomethyltransferase P48728
C0001122 Acidosis AMT 275 aminomethyltransferase P48728
C0011570 Mental Depression AMT 275 aminomethyltransferase P48728
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

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Last updated: August 19, 2024