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 |
---|---|---|---|---|---|
C1306459 | Primary malignant neoplasm | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C0010054 | Coronary Arteriosclerosis | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C0005779 | Blood Coagulation Disorders | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C1956346 | Coronary Artery Disease | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C1306589 | Congenital dyserythropoietic anemia, type II | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C0006826 | Malignant Neoplasms | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C0042880 | Vitamin K Deficiency | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C2873785 | Deficiency of factor V [labile] | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C0010068 | Coronary heart disease | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C0019069 | Hemophilia A | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C3494187 | Factor VIII Deficiency | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C0036631 | Seminoma | MCFD2 | 90411 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit | Q8NI22 |
C0024117 | Chronic Obstructive Airway Disease | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0025202 | melanoma | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0029408 | Degenerative polyarthritis | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0026769 | Multiple Sclerosis | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0004153 | Atherosclerosis | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0017636 | Glioblastoma | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0004623 | Bacterial Infections | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0037221 | Situs Inversus | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0002395 | Alzheimer's Disease | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0009319 | Colitis | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0023418 | leukemia | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0027873 | Neuromyelitis Optica | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0032463 | Polycythemia Vera | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
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