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 9101 - 9125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0026764 Multiple Myeloma SLC2A12 154091 solute carrier family 2 member 12 Q8TD20
C0006142 Malignant neoplasm of breast SLC2A12 154091 solute carrier family 2 member 12 Q8TD20
C0400966 Non-alcoholic Fatty Liver Disease SLC2A12 154091 solute carrier family 2 member 12 Q8TD20
C0011860 Diabetes Mellitus, Non-Insulin-Dependent PHOSPHO1 162466 phosphoethanolamine/phosphocholine phosphatase 1 Q8TCT1
C0029442 Osteomalacia PHOSPHO1 162466 phosphoethanolamine/phosphocholine phosphatase 1 Q8TCT1
C3887650 Adult Rickets PHOSPHO1 162466 phosphoethanolamine/phosphocholine phosphatase 1 Q8TCT1
C0027819 Neuroblastoma CERK 64781 ceramide kinase Q8TCT0
C0700095 Central neuroblastoma CERK 64781 ceramide kinase Q8TCT0
C0006142 Malignant neoplasm of breast CERK 64781 ceramide kinase Q8TCT0
C0028754 Obesity CERK 64781 ceramide kinase Q8TCT0
C0678222 Breast Carcinoma CERK 64781 ceramide kinase Q8TCT0
C1458155 Mammary Neoplasms CERK 64781 ceramide kinase Q8TCT0
C0543918 SCHIZOPHRENIA 10 CERK 64781 ceramide kinase Q8TCT0
C0027651 Neoplasms CERK 64781 ceramide kinase Q8TCT0
C1832661 ANOPHTHALMIA AND PULMONARY HYPOPLASIA CERK 64781 ceramide kinase Q8TCT0
C0009319 Colitis CERK 64781 ceramide kinase Q8TCT0
C0036220 Kaposi Sarcoma CERK 64781 ceramide kinase Q8TCT0
C2931007 Congenital disorder of glycosylation type 1X STT3B 201595 STT3 oligosaccharyltransferase complex catalytic subunit B Q8TCJ2
C3714756 Intellectual Disability STT3B 201595 STT3 oligosaccharyltransferase complex catalytic subunit B Q8TCJ2
C0041228 African Trypanosomiasis STT3B 201595 STT3 oligosaccharyltransferase complex catalytic subunit B Q8TCJ2
C0036572 Seizures STT3B 201595 STT3 oligosaccharyltransferase complex catalytic subunit B Q8TCJ2
C0282577 Congenital Disorders of Glycosylation STT3B 201595 STT3 oligosaccharyltransferase complex catalytic subunit B Q8TCJ2
C0015934 Fetal Growth Retardation STT3B 201595 STT3 oligosaccharyltransferase complex catalytic subunit B Q8TCJ2
C0025958 Microcephaly STT3B 201595 STT3 oligosaccharyltransferase complex catalytic subunit B Q8TCJ2
C0010417 Cryptorchidism STT3B 201595 STT3 oligosaccharyltransferase complex catalytic subunit B Q8TCJ2

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Last updated: August 19, 2024