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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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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:0070136 | autosomal dominant cutis laxa 2 | HGNC:3602 | Homo sapiens (human) | 10516 | FBLN5 |
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| DOID:0070135 | autosomal recessive cutis laxa type IA | RGD:2594 | Rattus norvegicus (Norway rat) | 29158 | Fbln5 |
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| DOID:0070135 | autosomal recessive cutis laxa type IA | HGNC:3602 | Homo sapiens (human) | 10516 | FBLN5 |
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| DOID:0070135 | autosomal recessive cutis laxa type IA | MGI:1346091 | Mus musculus (house mouse) | 23876 | Fbln5 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | WB:WBGene00006914 | Caenorhabditis elegans | 177626 | vha-5 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | WB:WBGene00006915 | Caenorhabditis elegans | 174743 | vha-6 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | WB:WBGene00006916 | Caenorhabditis elegans | 178219 | vha-7 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | MGI:104855 | Mus musculus (house mouse) | 21871 | Atp6v0a2 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0070133 | autosomal recessive cutis laxa type IB | HGNC:3219 | Homo sapiens (human) | 30008 | EFEMP2 |
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| DOID:0070133 | autosomal recessive cutis laxa type IB | MGI:1891209 | Mus musculus (house mouse) | 58859 | Efemp2 |
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| DOID:0070132 | autosomal recessive cutis laxa type IIIA | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:0070132 | autosomal recessive cutis laxa type IIIA | MGI:1888908 | Mus musculus (house mouse) | 56454 | Aldh18a1 |
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| DOID:0070131 | autosomal dominant cutis laxa 3 | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:0070131 | autosomal dominant cutis laxa 3 | MGI:1888908 | Mus musculus (house mouse) | 56454 | Aldh18a1 |
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| DOID:0070130 | autosomal dominant cutis laxa 1 | HGNC:3327 | Homo sapiens (human) | 2006 | ELN |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | MGI:1201780 | Mus musculus (house mouse) | 11964 | Atp6v1a |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | Xenbase:XB-GENE-990439 | Xenopus tropicalis (tropical clawed frog) | 407846 | st6gal2 |
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| DOID:0070128 | congenital nongoitrous hypothyroidism 6 | HGNC:11796 | Homo sapiens (human) | 7067 | THRA |
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| DOID:0070124 | congenital nongoitrous hypothyroidism 2 | HGNC:8622 | Homo sapiens (human) | 7849 | PAX8 |
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| DOID:0070123 | congenital nongoitrous hypothyroidism 4 | RGD:3910 | Rattus norvegicus (Norway rat) | 25653 | Tshb |
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| DOID:0070123 | congenital nongoitrous hypothyroidism 4 | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:0070122 | Meckel syndrome 8 | RGD:1591895 | Rattus norvegicus (Norway rat) | 689779 | Tctn2 |
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| DOID:0070122 | Meckel syndrome 8 | MGI:1915228 | Mus musculus (house mouse) | 67978 | Tctn2 |
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