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 47526 - 47550 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0017638 Glioma ATRN 8455 attractin O75882
C0574084 3-Methylglutaconic aciduria type 3 ATRN 8455 attractin O75882
C0334579 Anaplastic astrocytoma ATRN 8455 attractin O75882
C0023520 Leukodystrophy ATRN 8455 attractin O75882
C0021390 Inflammatory Bowel Diseases AGA 175 aspartylglucosaminidase P20933
C0009324 Ulcerative Colitis AGA 175 aspartylglucosaminidase P20933
C0085078 Lysosomal Storage Diseases AGA 175 aspartylglucosaminidase P20933
C0268225 Aspartylglucosaminuria AGA 175 aspartylglucosaminidase P20933
C0019196 Hepatitis C AGA 175 aspartylglucosaminidase P20933
C0162311 Androgenetic Alopecia AGA 175 aspartylglucosaminidase P20933
C0699791 Stomach Carcinoma AGA 175 aspartylglucosaminidase P20933
C0008325 Cholecystitis AGA 175 aspartylglucosaminidase P20933
C0085207 Gestational Diabetes AGA 175 aspartylglucosaminidase P20933
C0022104 Irritable Bowel Syndrome AGA 175 aspartylglucosaminidase P20933
C0036341 Schizophrenia AGA 175 aspartylglucosaminidase P20933
C0524620 Metabolic Syndrome X AGA 175 aspartylglucosaminidase P20933
C0019294 Hernia, Inguinal AGA 175 aspartylglucosaminidase P20933
C0011847 Diabetes AGA 175 aspartylglucosaminidase P20933
C0007570 Celiac Disease AGA 175 aspartylglucosaminidase P20933
C0038018 Spondylolysis AGA 175 aspartylglucosaminidase P20933
C0016202 Flatfoot AGA 175 aspartylglucosaminidase P20933
C0040128 Thyroid Diseases AGA 175 aspartylglucosaminidase P20933
C0235946 Cerebral atrophy AGA 175 aspartylglucosaminidase P20933
C2931840 Aspartylglucosamidase (AGA) deficiency AGA 175 aspartylglucosaminidase P20933
C0024623 Malignant neoplasm of stomach AGA 175 aspartylglucosaminidase P20933

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Last updated: August 19, 2024