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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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| DOID:0060300 | complement component 7 deficiency | HGNC:1346 | Homo sapiens (human) | 730 | C7 |
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| DOID:0050957 | spinocerebellar ataxia type 4 | HGNC:777 | Homo sapiens (human) | 463 | ZFHX3 |
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| DOID:0112189 | thyroid dyshormonogenesis 6 | HGNC:13273 | Homo sapiens (human) | 50506 | DUOX2 |
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| DOID:0081382 | amyotrophic lateral sclerosis type 28 | HGNC:31708 | Homo sapiens (human) | 29967 | LRP12 |
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| DOID:0110014 | age related macular degeneration 1 | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:2043 | hepatitis B | HGNC:5965 | Homo sapiens (human) | 3588 | IL10RB |
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| DOID:13810 | familial hypercholesterolemia | HGNC:4263 | Homo sapiens (human) | 2690 | GHR |
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| DOID:0110873 | holoprosencephaly 9 | HGNC:4318 | Homo sapiens (human) | 2736 | GLI2 |
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| DOID:0110149 | Charcot-Marie-Tooth disease type 1F | HGNC:7739 | Homo sapiens (human) | 4747 | NEFL |
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| DOID:0110445 | dilated cardiomyopathy 1KK | HGNC:23246 | Homo sapiens (human) | 84665 | MYPN |
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| DOID:0080038 | pycnodysostosis | HGNC:2536 | Homo sapiens (human) | 1513 | CTSK |
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| DOID:0110432 | dilated cardiomyopathy 1NN | HGNC:9829 | Homo sapiens (human) | 5894 | RAF1 |
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| DOID:0111631 | familial erythrocytosis 7 | HGNC:4824 | Homo sapiens (human) | 3040 | HBA2 |
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| DOID:0050715 | methylmalonic aciduria and homocystinuria type cblC | HGNC:9352 | Homo sapiens (human) | 5052 | PRDX1 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:24305 | Homo sapiens (human) | 9918 | NCAPD2 |
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| DOID:0111150 | autosomal dominant isolated ectopia lentis 1 | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:0111242 | congenital muscular dystrophy-dystroglycanopathy type A6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:0080565 | congenital disorder of glycosylation Im | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:2841 | asthma | HGNC:9591 | Homo sapiens (human) | 5729 | PTGDR |
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| DOID:0070396 | progressive leukoencephalopathy with ovarian failure | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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| DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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| DOID:0112122 | X-linked epilepsy with variable learning disabilities and behavior disorders | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:18697 | Homo sapiens (human) | 10973 | ASCC3 |
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