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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name ▲ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0001144 | Acne Vulgaris | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0027859 | Acoustic Neuroma | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
C0027859 | Acoustic Neuroma | CAT | 847 | catalase | P04040 |
C0027859 | Acoustic Neuroma | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0027859 | Acoustic Neuroma | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0027859 | Acoustic Neuroma | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0027859 | Acoustic Neuroma | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C2936664 | Acquired Hypogammaglobulinemia | CHIT1 | 1118 | chitinase 1 | Q13231 |
C2936664 | Acquired Hypogammaglobulinemia | NEIL1 | 79661 | nei like DNA glycosylase 1 | Q96FI4 |
C2936664 | Acquired Hypogammaglobulinemia | CD38 | 952 | CD38 molecule | P28907 |
C2936664 | Acquired Hypogammaglobulinemia | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
C2936664 | Acquired Hypogammaglobulinemia | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
C2936664 | Acquired Hypogammaglobulinemia | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C2936664 | Acquired Hypogammaglobulinemia | FCN2 | 2220 | ficolin 2 | Q15485 |
C0001175 | Acquired Immunodeficiency Syndrome | FUT1 | 2523 | fucosyltransferase 1 (H blood group) | P19526 |
C0001175 | Acquired Immunodeficiency Syndrome | GPI | 2821 | glucose-6-phosphate isomerase | P06744 |
C0001175 | Acquired Immunodeficiency Syndrome | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0001175 | Acquired Immunodeficiency Syndrome | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0001175 | Acquired Immunodeficiency Syndrome | PLA2G15 | 23659 | phospholipase A2 group XV | Q8NCC3 |
C0001175 | Acquired Immunodeficiency Syndrome | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
C0001175 | Acquired Immunodeficiency Syndrome | CD209 | 30835 | CD209 molecule | Q9NNX6 |
C0001175 | Acquired Immunodeficiency Syndrome | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
C0001175 | Acquired Immunodeficiency Syndrome | LGALS1 | 3956 | galectin 1 | P09382 |
C0001175 | Acquired Immunodeficiency Syndrome | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
C0001175 | Acquired Immunodeficiency Syndrome | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
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Last updated: August 19, 2024