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 13926 - 13950 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0027819 Neuroblastoma MGAT5B 146664 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B Q3V5L5
C0006826 Malignant Neoplasms MGAT5B 146664 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B Q3V5L5
C0153633 Malignant neoplasm of brain MGAT5B 146664 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B Q3V5L5
C2239176 Liver carcinoma MGAT5B 146664 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B Q3V5L5
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma MGAT5B 146664 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B Q3V5L5
C0020725 Type II Mucolipidosis GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0033788 Pseudo-Hurler Polydystrophy GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0878544 Cardiomyopathies GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C2673377 MUCOLIPIDOSIS II ALPHA/BETA (disorder) GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0019270 Hernia GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0085078 Lysosomal Storage Diseases GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C1306503 Congenital exomphalos GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0004352 Autistic Disorder GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0026697 Mucolipidoses GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0476254 Dyslexia GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0027651 Neoplasms GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0920296 Developmental reading disorder GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0013336 Dwarfism GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0344530 Congenital keratoglobus GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0036439 Scoliosis, unspecified GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C3714756 Intellectual Disability GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0018801 Heart failure GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C2673375 Mucolipidosis III Alpha Beta, Atypical GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0019294 Hernia, Inguinal GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906
C0010278 Craniosynostosis GNPTAB 79158 N-acetylglucosamine-1-phosphate transferase subunits alpha and beta Q3T906

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Last updated: August 19, 2024