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 |
---|---|---|---|---|---|
C0001342 | Acute periodontitis | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0001342 | Acute periodontitis | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
C0001342 | Acute periodontitis | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
C0001342 | Acute periodontitis | SMPD3 | 55512 | sphingomyelin phosphodiesterase 3 | Q9NY59 |
C0001342 | Acute periodontitis | MMP25 | 64386 | matrix metallopeptidase 25 | Q9NPA2 |
C0001342 | Acute periodontitis | SIGLEC5 | 8778 | sialic acid binding Ig like lectin 5 | O15389 |
C0001342 | Acute periodontitis | CD14 | 929 | CD14 molecule | P08571 |
C0001342 | Acute periodontitis | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0001344 | Acute pharyngitis | GALNS | 2588 | galactosamine (N-acetyl)-6-sulfatase | P34059 |
C0001344 | Acute pharyngitis | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0001361 | Acute tonsillitis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
C0001363 | Acute vascular insufficiency of intestine (disorder) | PCYT1A | 5130 | phosphate cytidylyltransferase 1, choline, alpha | P49585 |
C0001403 | Addison Disease | UGT2B28 | 54490 | UDP glucuronosyltransferase family 2 member B28 | Q9BY64 |
C0001403 | Addison Disease | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0001403 | Addison Disease | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
C0001403 | Addison Disease | HSD11B1 | 3290 | hydroxysteroid 11-beta dehydrogenase 1 | P28845 |
C0001403 | Addison Disease | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0001403 | Addison Disease | SGPL1 | 8879 | sphingosine-1-phosphate lyase 1 | O95470 |
C0001403 | Addison Disease | CD14 | 929 | CD14 molecule | P08571 |
C0001403 | Addison Disease | MICA | 100507436 | MHC class I polypeptide-related sequence A | Q29983 |
C0001403 | Addison Disease | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0001403 | Addison Disease | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0001403 | Addison Disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0001403 | Addison Disease | GAD2 | 2572 | glutamate decarboxylase 2 | Q05329 |
C0001403 | Addison Disease | HSD17B4 | 3295 | hydroxysteroid 17-beta dehydrogenase 4 | P51659 |
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Last updated: August 19, 2024