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 54001 - 54025 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0796059 Oculopalatoskeletal syndrome COLEC11 78989 collectin subfamily member 11 Q9BWP8
C3714756 Intellectual Disability COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0080174 Spina Bifida Occulta COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0243026 Sepsis COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0019693 HIV Infections COLEC11 78989 collectin subfamily member 11 Q9BWP8
C3714636 Pneumonitis COLEC11 78989 collectin subfamily member 11 Q9BWP8
C1836230 HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO COLEC11 78989 collectin subfamily member 11 Q9BWP8
C0010278 Craniosynostosis COLEC11 78989 collectin subfamily member 11 Q9BWP8
C2711227 Steatohepatitis ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0152018 Esophageal carcinoma ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C1621958 Glioblastoma Multiforme ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0162309 Adrenoleukodystrophy ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0015695 Fatty Liver ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0546837 Malignant neoplasm of esophagus ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0027126 Myotonic Dystrophy ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0027651 Neoplasms ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0038454 Cerebrovascular accident ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0032285 Pneumonia ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0011581 Depressive disorder ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0036341 Schizophrenia ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C1306459 Primary malignant neoplasm ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0004114 Astrocytoma ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0030567 Parkinson Disease ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0027697 Nephritis ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187
C0020179 Huntington Disease ST8SIA4 7903 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 Q92187

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Last updated: August 19, 2024