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 |
---|---|---|---|---|---|
C0241005 | Creatine phosphokinase serum increased | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C3279947 | NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C1837396 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C0018916 | Hemangioma | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C0398625 | Protein C Deficiency | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C0013274 | Patent ductus arteriosus | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C4317224 | Congenital disorder of glycosylation type 1q | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C0025958 | Microcephaly | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C0699743 | Congenital muscular dystrophy (disorder) | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C0272375 | Antithrombin III Deficiency | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C0039446 | Telangiectasis | DPM1 | 8813 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | O60762 |
C0040580 | Tracheal Diseases | DPEP3 | 64180 | dipeptidase 3 | Q9H4B8 |
C0010068 | Coronary heart disease | DPEP3 | 64180 | dipeptidase 3 | Q9H4B8 |
C0919267 | ovarian neoplasm | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
C4721610 | Carcinoma, Ovarian Epithelial | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
C0002395 | Alzheimer's Disease | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
C1140680 | Malignant neoplasm of ovary | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
C0010068 | Coronary heart disease | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
C0040580 | Tracheal Diseases | DPEP2 | 64174 | dipeptidase 2 | Q9H4A9 |
C0005683 | Urinary Bladder Calculi (disorder) | DPEP1 | 1800 | dipeptidase 1 | P16444 |
C0678222 | Breast Carcinoma | DPEP1 | 1800 | dipeptidase 1 | P16444 |
C0009402 | Colorectal Carcinoma | DPEP1 | 1800 | dipeptidase 1 | P16444 |
C0027651 | Neoplasms | DPEP1 | 1800 | dipeptidase 1 | P16444 |
C0006142 | Malignant neoplasm of breast | DPEP1 | 1800 | dipeptidase 1 | P16444 |
C1306459 | Primary malignant neoplasm | DPEP1 | 1800 | dipeptidase 1 | P16444 |
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