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 |
---|---|---|---|---|---|
C4721453 | Peripheral Nervous System Diseases | LYZ | 4069 | lysozyme | P61626 |
C4721453 | Peripheral Nervous System Diseases | PDHA1 | 5160 | pyruvate dehydrogenase E1 subunit alpha 1 | P08559 |
C4721453 | Peripheral Nervous System Diseases | ACER3 | 55331 | alkaline ceramidase 3 | Q9NUN7 |
C4721453 | Peripheral Nervous System Diseases | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C4721453 | Peripheral Nervous System Diseases | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
C4721453 | Peripheral Nervous System Diseases | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
C4721453 | Peripheral Nervous System Diseases | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
C4721453 | Peripheral Nervous System Diseases | AGPAT2 | 10555 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | O15120 |
C4721453 | Peripheral Nervous System Diseases | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
C4721453 | Peripheral Nervous System Diseases | CYP2U1 | 113612 | cytochrome P450 family 2 subfamily U member 1 | Q7Z449 |
C4721453 | Peripheral Nervous System Diseases | ACOT7 | 11332 | acyl-CoA thioesterase 7 | O00154 |
C4721453 | Peripheral Nervous System Diseases | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
C4721453 | Peripheral Nervous System Diseases | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C4721453 | Peripheral Nervous System Diseases | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C4721453 | Peripheral Nervous System Diseases | FOLR1 | 2348 | folate receptor alpha | P15328 |
C4721453 | Peripheral Nervous System Diseases | ALOX12 | 239 | arachidonate 12-lipoxygenase, 12S type | P18054 |
C4721453 | Peripheral Nervous System Diseases | GPX1 | 2876 | glutathione peroxidase 1 | P07203 |
C4721453 | Peripheral Nervous System Diseases | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
C4721453 | Peripheral Nervous System Diseases | MAG | 4099 | myelin associated glycoprotein | P20916 |
C4721453 | Peripheral Nervous System Diseases | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
C4721453 | Peripheral Nervous System Diseases | NCAM1 | 4684 | neural cell adhesion molecule 1 | P13591 |
C4721453 | Peripheral Nervous System Diseases | INPP5K | 51763 | inositol polyphosphate-5-phosphatase K | Q9BT40 |
C4721453 | Peripheral Nervous System Diseases | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
C4721453 | Peripheral Nervous System Diseases | PRNP | 5621 | prion protein | P04156 |
C4721453 | Peripheral Nervous System Diseases | PNPLA2 | 57104 | patatin like phospholipase domain containing 2 | Q96AD5 |
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Last updated: August 19, 2024