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 39251 - 39275 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C1306459 Primary malignant neoplasm NEU3 10825 neuraminidase 3 Q9UQ49
C0006826 Malignant Neoplasms NEU3 10825 neuraminidase 3 Q9UQ49
C1140680 Malignant neoplasm of ovary NEU3 10825 neuraminidase 3 Q9UQ49
C1621958 Glioblastoma Multiforme NEU4 129807 neuraminidase 4 Q8WWR8
C0027651 Neoplasms NEU4 129807 neuraminidase 4 Q8WWR8
C0700095 Central neuroblastoma NEU4 129807 neuraminidase 4 Q8WWR8
C0278878 Adult Glioblastoma NEU4 129807 neuraminidase 4 Q8WWR8
C0006826 Malignant Neoplasms NEU4 129807 neuraminidase 4 Q8WWR8
C0027819 Neuroblastoma NEU4 129807 neuraminidase 4 Q8WWR8
C0017636 Glioblastoma NEU4 129807 neuraminidase 4 Q8WWR8
C1306459 Primary malignant neoplasm NEU4 129807 neuraminidase 4 Q8WWR8
C0025958 Microcephaly NGLY1 55768 N-glycanase 1 Q96IV0
C1531647 Cerebral ventriculomegaly NGLY1 55768 N-glycanase 1 Q96IV0
C0270820 Gelastic Epilepsy NGLY1 55768 N-glycanase 1 Q96IV0
C1306459 Primary malignant neoplasm NGLY1 55768 N-glycanase 1 Q96IV0
C0085109 Corneal Neovascularization NGLY1 55768 N-glycanase 1 Q96IV0
C0036439 Scoliosis, unspecified NGLY1 55768 N-glycanase 1 Q96IV0
C4316812 Fibrinogen Deficiency NGLY1 55768 N-glycanase 1 Q96IV0
C0008489 Chorea NGLY1 55768 N-glycanase 1 Q96IV0
C0031117 Peripheral Neuropathy NGLY1 55768 N-glycanase 1 Q96IV0
C0699791 Stomach Carcinoma NGLY1 55768 N-glycanase 1 Q96IV0
C0010043 Corneal Ulcer NGLY1 55768 N-glycanase 1 Q96IV0
C0036572 Seizures NGLY1 55768 N-glycanase 1 Q96IV0
C0038379 Strabismus NGLY1 55768 N-glycanase 1 Q96IV0
C0221356 Brachycephaly NGLY1 55768 N-glycanase 1 Q96IV0

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Last updated: August 19, 2024