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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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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 | July 29, 2024 |
| Disease ID ▼ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070174 | spermatogenic failure 17 | HGNC:19218 | Homo sapiens (human) | 89869 | PLCZ1 |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:16253 | Homo sapiens (human) | 55304 | SPTLC3 |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:0070157 | hereditary sensory and autonomic neuropathy type 1C | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:0070152 | hereditary sensory and autonomic neuropathy type 1A | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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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:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:0070113 | Niemann-Pick disease type C1 | MGI:1097712 | Mus musculus (house mouse) | 18145 | Npc1 |
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| DOID:0070113 | Niemann-Pick disease type C1 | HGNC:7897 | Homo sapiens (human) | 4864 | NPC1 |
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| DOID:0070112 | Niemann-Pick disease type B | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:0070112 | Niemann-Pick disease type B | WB:WBGene00000211 | Caenorhabditis elegans | 174131 | asm-1 |
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| DOID:0070112 | Niemann-Pick disease type B | WB:WBGene00000212 | Caenorhabditis elegans | 181323 | asm-2 |
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| DOID:0070112 | Niemann-Pick disease type B | WB:WBGene00000213 | Caenorhabditis elegans | 176879 | asm-3 |
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| DOID:0070112 | Niemann-Pick disease type B | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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| DOID:0070111 | Niemann-Pick disease type A | WB:WBGene00000212 | Caenorhabditis elegans | 181323 | asm-2 |
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| DOID:0070111 | Niemann-Pick disease type A | WB:WBGene00000211 | Caenorhabditis elegans | 174131 | asm-1 |
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| DOID:0070111 | Niemann-Pick disease type A | WB:WBGene00000213 | Caenorhabditis elegans | 176879 | asm-3 |
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| DOID:0070111 | Niemann-Pick disease type A | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:0070111 | Niemann-Pick disease type A | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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| DOID:0070004 | myeloid neoplasm | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0060903 | thrombosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0060903 | thrombosis | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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| DOID:0060901 | lymphoplasmacytic lymphoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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