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 |
---|---|---|---|---|---|
C0041234 | Chagas Disease | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0152025 | Polyneuropathy | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0751406 | Post-Traumatic Osteoporosis | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0037199 | Sinusitis | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0004153 | Atherosclerosis | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0577631 | Carotid Atherosclerosis | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0002395 | Alzheimer's Disease | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0398650 | Immune thrombocytopenic purpura | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0268124 | Adenosine deaminase deficiency | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0600139 | Prostate carcinoma | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0281361 | Adenocarcinoma of pancreas | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0023452 | Childhood Acute Lymphoblastic Leukemia | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0024138 | Lupus Erythematosus, Discoid | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0025202 | melanoma | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0042373 | Vascular Diseases | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0162671 | MELAS Syndrome | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C1970827 | Phosphoribosylpyrophosphate Synthetase Superactivity | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C2700553 | Omenn Syndrome | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C1332979 | Childhood Lymphoma | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0238051 | Cerebral Angiitis | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0031090 | Periodontal Diseases | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0024312 | Lymphopenia | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0005684 | Malignant neoplasm of urinary bladder | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
C0086438 | Hypogammaglobulinemia | PNP | 4860 | purine nucleoside phosphorylase | P00491 |
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