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 |
---|---|---|---|---|---|
C0037221 | Situs Inversus | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C2239176 | Liver carcinoma | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C1567435 | Polycystic Kidney - body part | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0027651 | Neoplasms | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0023895 | Liver diseases | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0887850 | Polycystic Kidney, Type 1 Autosomal Dominant Disease | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0017168 | Gastroesophageal reflux disease | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0019163 | Hepatitis B | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0020445 | Hypercholesterolemia, Familial | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0022680 | Polycystic Kidney Diseases | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C3887499 | Renal cyst | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C1720416 | Episodic ataxia type 2 (disorder) | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0005283 | beta Thalassemia | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0085413 | Polycystic Kidney, Autosomal Dominant | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C1832884 | Hemiplegic migraine, familial type 1 | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0394006 | Dysequilibrium syndrome | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0678222 | Breast Carcinoma | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0006142 | Malignant neoplasm of breast | PRKCSH | 5589 | protein kinase C substrate 80K-H | P14314 |
C0524851 | Neurodegenerative Disorders | PRNP | 5621 | prion protein | P04156 |
C1852467 | Creutzfeldt-Jakob Disease, Sporadic | PRNP | 5621 | prion protein | P04156 |
C0162534 | Prion Diseases | PRNP | 5621 | prion protein | P04156 |
C0002395 | Alzheimer's Disease | PRNP | 5621 | prion protein | P04156 |
C0006142 | Malignant neoplasm of breast | PRNP | 5621 | prion protein | P04156 |
C0017495 | Gerstmann-Straussler-Scheinker Disease | PRNP | 5621 | prion protein | P04156 |
C0026650 | Movement Disorders | PRNP | 5621 | prion protein | P04156 |
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