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 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▼ |
---|---|---|---|---|---|
C0011849 | Diabetes Mellitus | TREH | 11181 | trehalase | O43280 |
C0027651 | Neoplasms | TREH | 11181 | trehalase | O43280 |
C2239176 | Liver carcinoma | TREH | 11181 | trehalase | O43280 |
C0022658 | Kidney Diseases | TREH | 11181 | trehalase | O43280 |
C0087012 | Ataxia, Spinocerebellar | TREH | 11181 | trehalase | O43280 |
C0037930 | Spinal Cord Neoplasms | TREH | 11181 | trehalase | O43280 |
C0011991 | Diarrhea | TREH | 11181 | trehalase | O43280 |
C0684249 | Carcinoma of lung | TREH | 11181 | trehalase | O43280 |
C1306459 | Primary malignant neoplasm | TREH | 11181 | trehalase | O43280 |
C0006826 | Malignant Neoplasms | PAPSS1 | 9061 | 3'-phosphoadenosine 5'-phosphosulfate synthase 1 | O43252 |
C2239176 | Liver carcinoma | PAPSS1 | 9061 | 3'-phosphoadenosine 5'-phosphosulfate synthase 1 | O43252 |
C0007131 | Non-Small Cell Lung Carcinoma | PAPSS1 | 9061 | 3'-phosphoadenosine 5'-phosphosulfate synthase 1 | O43252 |
C1306459 | Primary malignant neoplasm | PAPSS1 | 9061 | 3'-phosphoadenosine 5'-phosphosulfate synthase 1 | O43252 |
C0019163 | Hepatitis B | PAPSS1 | 9061 | 3'-phosphoadenosine 5'-phosphosulfate synthase 1 | O43252 |
C0027651 | Neoplasms | PAPSS1 | 9061 | 3'-phosphoadenosine 5'-phosphosulfate synthase 1 | O43252 |
C0004782 | Basal Ganglia Diseases | ST8SIA3 | 51046 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 | O43173 |
C0006826 | Malignant Neoplasms | ST8SIA3 | 51046 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 | O43173 |
C0036341 | Schizophrenia | ST8SIA3 | 51046 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 | O43173 |
C0027651 | Neoplasms | ST8SIA3 | 51046 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 | O43173 |
C1306459 | Primary malignant neoplasm | ST8SIA3 | 51046 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 | O43173 |
C0023467 | Leukemia, Myelocytic, Acute | ST8SIA3 | 51046 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3 | O43173 |
C0020437 | Hypercalcemia | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0558356 | Malignant melanoma of eye | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0085682 | Hypophosphatemia | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0001175 | Acquired Immunodeficiency Syndrome | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024