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 |
---|---|---|---|---|---|
C0001175 | Acquired Immunodeficiency Syndrome | GPAT3 | 84803 | glycerol-3-phosphate acyltransferase 3 | Q53EU6 |
C0001175 | Acquired Immunodeficiency Syndrome | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
C0001175 | Acquired Immunodeficiency Syndrome | CD14 | 929 | CD14 molecule | P08571 |
C0001175 | Acquired Immunodeficiency Syndrome | UNG | 7374 | uracil DNA glycosylase | P13051 |
C0001175 | Acquired Immunodeficiency Syndrome | MICA | 100507436 | MHC class I polypeptide-related sequence A | Q29983 |
C0001175 | Acquired Immunodeficiency Syndrome | CYP4F3 | 4051 | cytochrome P450 family 4 subfamily F member 3 | Q08477 |
C0001175 | Acquired Immunodeficiency Syndrome | PLAUR | 5329 | plasminogen activator, urokinase receptor | Q03405 |
C0001175 | Acquired Immunodeficiency Syndrome | PRNP | 5621 | prion protein | F7VJQ1 |
C0001175 | Acquired Immunodeficiency Syndrome | BST2 | 684 | bone marrow stromal cell antigen 2 | Q10589 |
C0001206 | Acromegaly | CALR | 811 | calreticulin | P27797 |
C0001206 | Acromegaly | KL | 9365 | klotho | Q9UEF7 |
C0001206 | Acromegaly | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C0001206 | Acromegaly | ALPP | 250 | alkaline phosphatase, placental | P05187 |
C0001206 | Acromegaly | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
C0001206 | Acromegaly | HSD11B1 | 3290 | hydroxysteroid 11-beta dehydrogenase 1 | P28845 |
C0001206 | Acromegaly | LGALS3 | 3958 | galectin 3 | P17931 |
C0001206 | Acromegaly | LPL | 4023 | lipoprotein lipase | P06858 |
C0001206 | Acromegaly | NAMPT | 10135 | nicotinamide phosphoribosyltransferase | P43490 |
C0001206 | Acromegaly | RENBP | 5973 | renin binding protein | P51606 |
C0001206 | Acromegaly | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
C0001206 | Acromegaly | DGCR2 | 9993 | DiGeorge syndrome critical region gene 2 | P98153 |
C0001231 | ACTH Syndrome, Ectopic | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
C0001231 | ACTH Syndrome, Ectopic | HSD11B2 | 3291 | hydroxysteroid 11-beta dehydrogenase 2 | P80365 |
C0001261 | Actinomycosis | CAT | 847 | catalase | P04040 |
C0001306 | Acute alcoholic liver disease | CEACAM5 | 1048 | CEA cell adhesion molecule 5 | P06731 |
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Last updated: August 19, 2024