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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:0110633 | rigid spine muscular dystrophy 1 | HGNC:15999 | Homo sapiens (human) | 57190 | SELENON |
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| DOID:10652 | Alzheimer's disease | HGNC:6893 | Homo sapiens (human) | 4137 | MAPT |
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| DOID:10652 | Alzheimer's disease | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:2841 | asthma | HGNC:1030 | Homo sapiens (human) | 624 | BDKRB2 |
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| DOID:12716 | newborn respiratory distress syndrome | RGD:3665 | Rattus norvegicus (Norway rat) | 24773 | Sftpa1 |
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| DOID:12716 | newborn respiratory distress syndrome | RGD:3667 | Rattus norvegicus (Norway rat) | 25350 | Sftpd |
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| DOID:12716 | newborn respiratory distress syndrome | RGD:621700 | Rattus norvegicus (Norway rat) | 192155 | Sftpb |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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| DOID:0110052 | amelogenesis imperfecta type 1B | HGNC:3344 | Homo sapiens (human) | 10117 | ENAM |
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| DOID:811 | lipodystrophy | HGNC:15832 | Homo sapiens (human) | 26580 | BSCL2 |
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| DOID:10584 | retinitis pigmentosa | HGNC:17340 | Homo sapiens (human) | 10594 | PRPF8 |
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| DOID:0110862 | congenital stationary night blindness autosomal dominant 1 | MGI:97914 | Mus musculus (house mouse) | 212541 | Rho |
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| DOID:5812 | MHC class II deficiency | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:10587 | Krabbe disease | MGI:95636 | Mus musculus (house mouse) | 14420 | Galc |
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| DOID:11476 | osteoporosis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:10825 | essential hypertension | MGI:97362 | Mus musculus (house mouse) | 18127 | Nos3 |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:7166 | Homo sapiens (human) | 4313 | MMP2 |
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| DOID:0110964 | brachydactyly type A1 | HGNC:5956 | Homo sapiens (human) | 3549 | IHH |
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| DOID:14504 | Niemann-Pick disease | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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| DOID:0090019 | sitosterolemia | HGNC:13886 | Homo sapiens (human) | 64240 | ABCG5 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0080093 | myofibrillar myopathy 2 | MGI:88516 | Mus musculus (house mouse) | 12955 | Cryab |
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| DOID:13515 | tuberous sclerosis | MGI:1929183 | Mus musculus (house mouse) | 64930 | Tsc1 |
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| DOID:0090060 | Wolcott-Rallison syndrome | MGI:1341830 | Mus musculus (house mouse) | 13666 | Eif2ak3 |
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| DOID:6000 | congestive heart failure | HGNC:7939 | Homo sapiens (human) | 4878 | NPPA |
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