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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0112237 | lissencephaly 1 | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:11247 | disseminated intravascular coagulation | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12541 | Homo sapiens (human) | 54600 | UGT1A9 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:3132 | porphyria cutanea tarda | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:10591 | pre-eclampsia | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:9970 | obesity | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:11981 | morbid obesity | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:10933 | obsessive-compulsive disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:10952 | nephritis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0110961 | atypical Gaucher's disease due to saposin c deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:1324 | lung cancer | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:1826 | epilepsy | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:4947 | cholangiocarcinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:2018 | hyperinsulinism | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:11400 | pyelonephritis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:10320 | asbestosis | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:0110853 | rhizomelic chondrodysplasia punctata type 3 | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:783 | end stage renal disease | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:1793 | pancreatic cancer | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:0060704 | lymphoproliferative syndrome | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:14330 | Parkinson's disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:8947 | diabetic retinopathy | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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