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 |
---|---|---|---|---|---|
C0524620 | Metabolic Syndrome X | APRT | 353 | adenine phosphoribosyltransferase | P07741 |
C0524620 | Metabolic Syndrome X | IGF2R | 3482 | insulin like growth factor 2 receptor | P11717 |
C0524620 | Metabolic Syndrome X | INPPL1 | 3636 | inositol polyphosphate phosphatase like 1 | O15357 |
C0524620 | Metabolic Syndrome X | LYZ | 4069 | lysozyme | P61626 |
C0524620 | Metabolic Syndrome X | OGG1 | 4968 | 8-oxoguanine DNA glycosylase | O15527 |
C0524620 | Metabolic Syndrome X | PC | 5091 | pyruvate carboxylase | P11498 |
C0524620 | Metabolic Syndrome X | ENPP1 | 5167 | ectonucleotide pyrophosphatase/phosphodiesterase 1 | P22413 |
C0524620 | Metabolic Syndrome X | PDHA1 | 5160 | pyruvate dehydrogenase E1 subunit alpha 1 | P08559 |
C0524620 | Metabolic Syndrome X | PKM | 5315 | pyruvate kinase M1/2 | P14618 |
C0524620 | Metabolic Syndrome X | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0524620 | Metabolic Syndrome X | NANS | 54187 | N-acetylneuraminate synthase | Q9NR45 |
C0524620 | Metabolic Syndrome X | UGT1A7 | 54577 | UDP glucuronosyltransferase family 1 member A7 | Q9HAW7 |
C0524620 | Metabolic Syndrome X | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0524620 | Metabolic Syndrome X | UGT1A10 | 54575 | UDP glucuronosyltransferase family 1 member A10 | Q9HAW8 |
C0524620 | Metabolic Syndrome X | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
C0524620 | Metabolic Syndrome X | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C0524620 | Metabolic Syndrome X | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C0524620 | Metabolic Syndrome X | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0524620 | Metabolic Syndrome X | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0524620 | Metabolic Syndrome X | G6PC2 | 57818 | glucose-6-phosphatase catalytic subunit 2 | Q9NQR9 |
C0524620 | Metabolic Syndrome X | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0524620 | Metabolic Syndrome X | NEIL1 | 79661 | nei like DNA glycosylase 1 | Q96FI4 |
C0524620 | Metabolic Syndrome X | CANX | 821 | calnexin | P27824 |
C0524620 | Metabolic Syndrome X | CALR | 811 | calreticulin | P27797 |
C0524620 | Metabolic Syndrome X | KL | 9365 | klotho | Q9UEF7 |
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Last updated: August 19, 2024