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 ▲ |
---|---|---|---|---|---|
C0004096 | Asthma | PIP5K1B | 8395 | phosphatidylinositol-4-phosphate 5-kinase type 1 beta | O14986 |
C0235974 | Pancreatic carcinoma | PIP5K1B | 8395 | phosphatidylinositol-4-phosphate 5-kinase type 1 beta | O14986 |
C1561643 | Chronic Kidney Diseases | PIP5K1B | 8395 | phosphatidylinositol-4-phosphate 5-kinase type 1 beta | O14986 |
C1856689 | FRIEDREICH ATAXIA 1 | PIP5K1B | 8395 | phosphatidylinositol-4-phosphate 5-kinase type 1 beta | O14986 |
C0022661 | Kidney Failure, Chronic | PIP5K1B | 8395 | phosphatidylinositol-4-phosphate 5-kinase type 1 beta | O14986 |
C0029456 | Osteoporosis | PIP5K1B | 8395 | phosphatidylinositol-4-phosphate 5-kinase type 1 beta | O14986 |
C0346647 | Malignant neoplasm of pancreas | PIP5K1B | 8395 | phosphatidylinositol-4-phosphate 5-kinase type 1 beta | O14986 |
C0011849 | Diabetes Mellitus | PIP5K1B | 8395 | phosphatidylinositol-4-phosphate 5-kinase type 1 beta | O14986 |
C0006142 | Malignant neoplasm of breast | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0086132 | Depressive Symptoms | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0684249 | Carcinoma of lung | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0699790 | Colon Carcinoma | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0431399 | Familial aplasia of the vermis | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0007102 | Malignant tumor of colon | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0026850 | Muscular Dystrophy | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0002736 | Amyotrophic Lateral Sclerosis | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0278878 | Adult Glioblastoma | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0017636 | Glioblastoma | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0023473 | Myeloid Leukemia, Chronic | AGPAT2 | 10555 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | O15120 |
C0023787 | Lipodystrophy | AGPAT2 | 10555 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | O15120 |
C0029463 | Osteosarcoma | AGPAT2 | 10555 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | O15120 |
C0158981 | Neonatal diabetes mellitus | AGPAT2 | 10555 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | O15120 |
C1720863 | Congenital Generalized Lipodystrophy Type 2 | AGPAT2 | 10555 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | O15120 |
C1720862 | Congenital Generalized Lipodystrophy Type 1 | AGPAT2 | 10555 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | O15120 |
C0027051 | Myocardial Infarction | AGPAT2 | 10555 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | O15120 |
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