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 48201 - 48225 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0011847 Diabetes CS 1431 citrate synthase O75390
C0020459 Hyperinsulinism CS 1431 citrate synthase O75390
C0011860 Diabetes Mellitus, Non-Insulin-Dependent CS 1431 citrate synthase O75390
C0451819 Simple obesity CS 1431 citrate synthase O75390
C0004352 Autistic Disorder CS 1431 citrate synthase O75390
C1140680 Malignant neoplasm of ovary CS 1431 citrate synthase O75390
C0020550 Hyperthyroidism CS 1431 citrate synthase O75390
C1456418 Absence of muscle CS 1431 citrate synthase O75390
C0919267 ovarian neoplasm CS 1431 citrate synthase O75390
C0017075 Ganglioneuroma CS 1431 citrate synthase O75390
C0011570 Mental Depression CS 1431 citrate synthase O75390
C0014118 Endocarditis CS 1431 citrate synthase O75390
C0151744 Myocardial Ischemia CS 1431 citrate synthase O75390
C0235527 Heart Failure, Right-Sided CS 1431 citrate synthase O75390
C0033860 Psoriasis CS 1431 citrate synthase O75390
C0011991 Diarrhea CRYL1 51084 crystallin lambda 1 Q9Y2S2
C0678222 Breast Carcinoma CRYL1 51084 crystallin lambda 1 Q9Y2S2
C0017536 Giardiasis CRYL1 51084 crystallin lambda 1 Q9Y2S2
C0154301 Acquired thrombocytopenia CRYL1 51084 crystallin lambda 1 Q9Y2S2
C0015934 Fetal Growth Retardation CRYL1 51084 crystallin lambda 1 Q9Y2S2
C0345905 Intrahepatic Cholangiocarcinoma CRYL1 51084 crystallin lambda 1 Q9Y2S2
C0013336 Dwarfism CRYL1 51084 crystallin lambda 1 Q9Y2S2
C2239176 Liver carcinoma CRYL1 51084 crystallin lambda 1 Q9Y2S2
C0002875 Cooley's anemia CRYL1 51084 crystallin lambda 1 Q9Y2S2
C3805278 Extrahepatic Cholangiocarcinoma CRYL1 51084 crystallin lambda 1 Q9Y2S2

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Last updated: August 19, 2024