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 |
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DisGeNET | July 29, 2024 |
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