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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0110569 | autosomal dominant nonsyndromic deafness 44 | HGNC:18111 | Homo sapiens (human) | 152137 | CCDC50 |
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| DOID:0014667 | disease of metabolism | HGNC:11289 | Homo sapiens (human) | 6720 | SREBF1 |
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| DOID:0110509 | autosomal recessive nonsyndromic deafness 53 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0080954 | arthrogryposis multiplex congenita | HGNC:12712 | Homo sapiens (human) | 26276 | VPS33B |
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| DOID:74 | hematopoietic system disease | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:3689 | brachial plexus neuritis | HGNC:7323 | Homo sapiens (human) | 10801 | SEPTIN9 |
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| DOID:1324 | lung cancer | HGNC:7127 | Homo sapiens (human) | 4292 | MLH1 |
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| DOID:0060645 | chronic recurrent multifocal osteomyelitis | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:1070 | primary open angle glaucoma | HGNC:7176 | Homo sapiens (human) | 4318 | MMP9 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:4938 | Homo sapiens (human) | 3113 | HLA-DPA1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:29182 | Homo sapiens (human) | 22897 | CEP164 |
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| DOID:0050742 | nicotine dependence | HGNC:15963 | Homo sapiens (human) | 8973 | CHRNA6 |
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| DOID:13608 | biliary atresia | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0111345 | transient bullous dermolysis of the newborn | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0111235 | congenital muscular dystrophy-dystroglycanopathy type A12 | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:5287 | Homo sapiens (human) | 3351 | HTR1B |
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| DOID:1612 | breast cancer | HGNC:9277 | Homo sapiens (human) | 8493 | PPM1D |
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| DOID:1340 | pure red-cell aplasia | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0050419 | complement factor I deficiency | HGNC:5394 | Homo sapiens (human) | 3426 | CFI |
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| DOID:5419 | schizophrenia | HGNC:18601 | Homo sapiens (human) | 65078 | RTN4R |
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| DOID:0050534 | congenital stationary night blindness | HGNC:4689 | Homo sapiens (human) | 3000 | GUCY2D |
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| DOID:0081267 | graft-versus-host disease | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:0110734 | neurodegeneration with brain iron accumulation | HGNC:3976 | Homo sapiens (human) | 2495 | FTH1 |
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| DOID:9120 | amyloidosis | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:612 | primary immunodeficiency disease | HGNC:8086 | Homo sapiens (human) | 4938 | OAS1 |
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