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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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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:4795 | GM2 gangliosidosis, AB variant | MGI:95762 | Mus musculus (house mouse) | 14667 | Gm2a |
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| DOID:850 | lung disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
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| DOID:10609 | rickets | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:9743 | diabetic neuropathy | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:0060639 | permanent neonatal diabetes mellitus | MGI:96573 | Mus musculus (house mouse) | 16334 | Ins2 |
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| DOID:2746 | glycogen storage disease V | HGNC:9726 | Homo sapiens (human) | 5837 | PYGM |
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| DOID:13141 | uveitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:10763 | hypertension | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:14692 | Smith-Lemli-Opitz syndrome | HGNC:2860 | Homo sapiens (human) | 1717 | DHCR7 |
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| DOID:14497 | Wolman disease | MGI:96789 | Mus musculus (house mouse) | 16889 | Lipa |
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| DOID:1561 | cognitive disorder | MGI:88470 | Mus musculus (house mouse) | 12846 | Comt |
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| DOID:0060363 | glycerol kinase deficiency | HGNC:4289 | Homo sapiens (human) | 2710 | GK |
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| DOID:783 | end stage renal disease | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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| DOID:10652 | Alzheimer's disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:1168 | familial hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:0110870 | congenital stationary night blindness 1A | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0050812 | spondyloepimetaphyseal dysplasia, Pakistani type | HGNC:8604 | Homo sapiens (human) | 9060 | PAPSS2 |
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| DOID:0080070 | mucolipidosis II alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:3347 | osteosarcoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0110515 | autosomal recessive nonsyndromic deafness 63 | HGNC:25033 | Homo sapiens (human) | 220074 | LRTOMT |
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| DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:1056 | oculocerebrorenal syndrome | HGNC:8108 | Homo sapiens (human) | 4952 | OCRL |
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| DOID:0111673 | Saul-Wilson syndrome | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:0111442 | optic atrophy 9 | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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