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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:0060355 | amyotrophic lateral sclerosis type 22 | MGI:1095410 | Mus musculus (house mouse) | 22145 | Tuba4a |
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| DOID:0060355 | amyotrophic lateral sclerosis type 22 | HGNC:12407 | Homo sapiens (human) | 7277 | TUBA4A |
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| DOID:0060354 | Stormorken syndrome | RGD:1306831 | Rattus norvegicus (Norway rat) | 361618 | Stim1 |
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| DOID:0060354 | Stormorken syndrome | MGI:107476 | Mus musculus (house mouse) | 20866 | Stim1 |
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| DOID:0060354 | Stormorken syndrome | FB:FBgn0045073 | Drosophila melanogaster (fruit fly) | 32556 | Stim |
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| DOID:0060354 | Stormorken syndrome | HGNC:11386 | Homo sapiens (human) | 6786 | STIM1 |
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| DOID:0060354 | Stormorken syndrome | WB:WBGene00021910 | Caenorhabditis elegans | 175201 | stim-1 |
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| DOID:0060352 | Kleefstra syndrome 1 | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
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| DOID:0060352 | Kleefstra syndrome 1 | HGNC:24650 | Homo sapiens (human) | 79813 | EHMT1 |
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| DOID:0060352 | Kleefstra syndrome 1 | MGI:1924933 | Mus musculus (house mouse) | 77683 | Ehmt1 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | SGD:S000004484 | Saccharomyces cerevisiae S288C | 854986 | APT1 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | HGNC:626 | Homo sapiens (human) | 353 | APRT |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | FB:FBgn0000109 | Drosophila melanogaster (fruit fly) | 48224 | Aprt |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | SGD:S000002849 | Saccharomyces cerevisiae S288C | 852051 | APT2 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | RGD:1307758 | Rattus norvegicus (Norway rat) | 292072 | Aprt |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | MGI:88061 | Mus musculus (house mouse) | 11821 | Aprt |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | WB:WBGene00020557 | Caenorhabditis elegans | 172232 | aprt-1 |
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| DOID:0060349 | microcephaly with or without chorioretinopathy, lymphedema, or mental retardation | HGNC:6388 | Homo sapiens (human) | 3832 | KIF11 |
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| DOID:0060348 | hypoparathyroidism-retardation-dysmorphism syndrome | SGD:S000000809 | Saccharomyces cerevisiae S288C | 856724 | PAC2 |
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| DOID:0060348 | hypoparathyroidism-retardation-dysmorphism syndrome | HGNC:4172 | Homo sapiens (human) | 2625 | GATA3 |
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| DOID:0060348 | hypoparathyroidism-retardation-dysmorphism syndrome | HGNC:11582 | Homo sapiens (human) | 6905 | TBCE |
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| DOID:0060342 | acromelic frontonasal dysostosis | HGNC:29316 | Homo sapiens (human) | 57688 | ZSWIM6 |
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| DOID:0060341 | agnathia-otocephaly complex | MGI:1336209 | Mus musculus (house mouse) | 216131 | Trappc10 |
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| DOID:0060341 | agnathia-otocephaly complex | MGI:97712 | Mus musculus (house mouse) | 18933 | Prrx1 |
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| DOID:0060341 | agnathia-otocephaly complex | HGNC:3814 | Homo sapiens (human) | 8928 | FOXH1 |
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