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 |
---|---|---|---|---|---|
C0036572 | Seizures | GPC1 | 2817 | glypican 1 | P35052 |
C0678222 | Breast Carcinoma | GPC1 | 2817 | glypican 1 | P35052 |
C4520983 | Congenital atresia of extrahepatic bile duct | GPC1 | 2817 | glypican 1 | P35052 |
C1335302 | Pancreatic Ductal Adenocarcinoma | GPC1 | 2817 | glypican 1 | P35052 |
C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | GPC1 | 2817 | glypican 1 | P35052 |
C0027651 | Neoplasms | GPC1 | 2817 | glypican 1 | P35052 |
C0017638 | Glioma | GPC1 | 2817 | glypican 1 | P35052 |
C1861735 | Dementia, familial Danish | GPC1 | 2817 | glypican 1 | P35052 |
C0006012 | Borderline Personality Disorder | GPC1 | 2817 | glypican 1 | P35052 |
C0017636 | Glioblastoma | GPC1 | 2817 | glypican 1 | P35052 |
C0235782 | Gallbladder Carcinoma | GPC1 | 2817 | glypican 1 | P35052 |
C0376358 | Malignant neoplasm of prostate | GPC1 | 2817 | glypican 1 | P35052 |
C1458155 | Mammary Neoplasms | GPC1 | 2817 | glypican 1 | P35052 |
C0392514 | Hereditary hemochromatosis | GPC1 | 2817 | glypican 1 | P35052 |
C0235991 | Small for gestational age (disorder) | GPC1 | 2817 | glypican 1 | P35052 |
C0002448 | Ameloblastoma | GPC1 | 2817 | glypican 1 | P35052 |
C3494506 | Pseudohypoparathyroidism, Type Ia | GPC1 | 2817 | glypican 1 | P35052 |
C0279626 | Squamous cell carcinoma of esophagus | GPC1 | 2817 | glypican 1 | P35052 |
C0206698 | Cholangiocarcinoma | GPC1 | 2817 | glypican 1 | P35052 |
C0013264 | Muscular Dystrophy, Duchenne | GPC1 | 2817 | glypican 1 | P35052 |
C0862312 | Epithelioid mesothelioma, malignant | GPC1 | 2817 | glypican 1 | P35052 |
C0009402 | Colorectal Carcinoma | GPC1 | 2817 | glypican 1 | P35052 |
C0699790 | Colon Carcinoma | GPC1 | 2817 | glypican 1 | P35052 |
C2931404 | Albright's hereditary osteodystrophy | GPC1 | 2817 | glypican 1 | P35052 |
C0036341 | Schizophrenia | GPC1 | 2817 | glypican 1 | P35052 |
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