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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:14330 | Parkinson's disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:418 | systemic scleroderma | FB:FBgn0013763 | Drosophila melanogaster (fruit fly) | 36868 | Idgf6 |
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| DOID:10584 | retinitis pigmentosa | SGD:S000003222 | Saccharomyces cerevisiae S288C | 852639 | HXK2 |
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| DOID:9119 | acute myeloid leukemia | MGI:96413 | Mus musculus (house mouse) | 15926 | Idh1 |
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| DOID:2841 | asthma | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:12858 | Huntington's disease | RGD:3000 | Rattus norvegicus (Norway rat) | 25608 | Lep |
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| DOID:9870 | galactosemia | SGD:S000005646 | Saccharomyces cerevisiae S288C | 854287 | GCY1 |
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| DOID:10907 | microcephaly | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:0050865 | tongue squamous cell carcinoma | MGI:96955 | Mus musculus (house mouse) | 17254 | Slc3a2 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | WB:WBGene00020375 | Caenorhabditis elegans | 172305 | pigv-1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:12716 | newborn respiratory distress syndrome | ZFIN:ZDB-GENE-030131-8022 | Danio rerio (zebrafish) | 570459 | ndst1b |
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| DOID:0050830 | peripheral artery disease | MGI:106675 | Mus musculus (house mouse) | 11450 | Adipoq |
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| DOID:0080411 | familial adenomatous polyposis 3 | SGD:S000005403 | Saccharomyces cerevisiae S288C | 854114 | NTG2 |
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| DOID:3083 | chronic obstructive pulmonary disease | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:16066 | Homo sapiens (human) | 55331 | ACER3 |
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| DOID:13241 | Behcet's disease | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:8534 | gastroesophageal reflux disease | MGI:1346060 | Mus musculus (house mouse) | 24088 | Tlr2 |
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| DOID:1596 | depressive disorder | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0050474 | Netherton syndrome | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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| DOID:1214 | tympanosclerosis | MGI:97370 | Mus musculus (house mouse) | 18605 | Enpp1 |
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| DOID:10763 | hypertension | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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| DOID:0060445 | congenital stromal corneal dystrophy | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:2537 | inflammatory and toxic neuropathy | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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