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 ▼ |
---|---|---|---|---|---|
C2239176 | Liver carcinoma | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0037274 | Dermatologic disorders | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C1134719 | Invasive Ductal Breast Carcinoma | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0023895 | Liver diseases | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0027051 | Myocardial Infarction | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0406811 | Reticulate acropigmentation of Kitamura | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0684249 | Carcinoma of lung | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0007124 | Noninfiltrating Intraductal Carcinoma | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0018801 | Heart failure | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0678222 | Breast Carcinoma | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0018802 | Congestive heart failure | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0036341 | Schizophrenia | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0158623 | Congenital anomaly of coronary artery | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0025958 | Microcephaly | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C1292778 | Chronic myeloproliferative disorder | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0006142 | Malignant neoplasm of breast | POFUT1 | 23509 | protein O-fucosyltransferase 1 | Q9H488 |
C0005586 | Bipolar Disorder | RBKS | 64080 | ribokinase | Q9H477 |
C0036341 | Schizophrenia | RBKS | 64080 | ribokinase | Q9H477 |
C0041296 | Tuberculosis | RBKS | 64080 | ribokinase | Q9H477 |
C0019154 | Hepatic Vein Thrombosis | PIGM | 93183 | phosphatidylinositol glycan anchor biosynthesis class M | Q9H3S5 |
C0494475 | Tonic - clonic seizures | PIGM | 93183 | phosphatidylinositol glycan anchor biosynthesis class M | Q9H3S5 |
C0042487 | Venous Thrombosis | PIGM | 93183 | phosphatidylinositol glycan anchor biosynthesis class M | Q9H3S5 |
C0014544 | Epilepsy | PIGM | 93183 | phosphatidylinositol glycan anchor biosynthesis class M | Q9H3S5 |
C0022333 | Jacksonian Seizure | PIGM | 93183 | phosphatidylinositol glycan anchor biosynthesis class M | Q9H3S5 |
C4048158 | Convulsions | PIGM | 93183 | phosphatidylinositol glycan anchor biosynthesis class M | Q9H3S5 |
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