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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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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:12583 | velocardiofacial syndrome | HGNC:17019 | Homo sapiens (human) | 144165 | PRICKLE1 |
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| DOID:1826 | epilepsy | HGNC:672 | Homo sapiens (human) | 391 | RHOG |
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| DOID:3070 | high grade glioma | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:0060956 | dystonia 37, early-onset with striatal lesions | FB:FBgn0033737 | Drosophila melanogaster (fruit fly) | 36360 | Nup54 |
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| DOID:1094 | attention deficit hyperactivity disorder | WB:WBGene00006541 | Caenorhabditis elegans | 181639 | tbh-1 |
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| DOID:1574 | alcohol use disorder | MGI:99659 | Mus musculus (house mouse) | 20190 | Ryr1 |
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| DOID:4500 | hypokalemia | HGNC:18140 | Homo sapiens (human) | 51458 | RHCG |
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| DOID:3981 | pantothenate kinase-associated neurodegeneration | HGNC:11140 | Homo sapiens (human) | 6620 | SNCB |
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| DOID:8778 | Crohn's disease | MGI:104887 | Mus musculus (house mouse) | 14775 | Gpx1 |
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| DOID:0060496 | respiratory allergy | HGNC:3538 | Homo sapiens (human) | 2150 | F2RL1 |
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| DOID:9775 | diastolic heart failure | WB:WBGene00000039 | Caenorhabditis elegans | 180780 | acn-1 |
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| DOID:114 | heart disease | MGI:2155600 | Mus musculus (house mouse) | 140781 | Myh7 |
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| DOID:4947 | cholangiocarcinoma | MGI:3576092 | Mus musculus (house mouse) | 394434 | Ugt1a9 |
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| DOID:0060643 | primary sclerosing cholangitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3211 | lysosomal storage disease | HGNC:318 | Homo sapiens (human) | 175 | AGA |
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| DOID:0050477 | Liddle syndrome | RGD:3639 | Rattus norvegicus (Norway rat) | 25122 | Scnn1a |
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| DOID:162 | cancer | MGI:1934234 | Mus musculus (house mouse) | 108083 | Pip4k2b |
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| DOID:1289 | neurodegenerative disease | MGI:1341865 | Mus musculus (house mouse) | 17169 | Mark3 |
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| DOID:3082 | interstitial lung disease | MGI:109515 | Mus musculus (house mouse) | 20390 | Sftpd |
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| DOID:0112040 | non-syndromic X-linked intellectual disability 100 | MGI:108389 | Mus musculus (house mouse) | 16571 | Kif4 |
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| DOID:0050628 | advanced sleep phase syndrome | HGNC:8846 | Homo sapiens (human) | 8864 | PER2 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:7910 | Homo sapiens (human) | 4869 | NPM1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:8064 | Homo sapiens (human) | 8021 | NUP214 |
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| DOID:0110681 | congenital myasthenic syndrome 2A | WB:WBGene00006797 | Caenorhabditis elegans | 172150 | unc-63 |
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| DOID:0110808 | hereditary spastic paraplegia 56 | HGNC:20582 | Homo sapiens (human) | 113612 | CYP2U1 |
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