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GlyTouCan
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
LM-GlycoRepo
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:2841 | asthma | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:4483 | rhinitis | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:0081378 | amyotrophic lateral sclerosis type 24 | HGNC:18591 | Homo sapiens (human) | 91754 | NEK9 |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:18591 | Homo sapiens (human) | 91754 | NEK9 |
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| DOID:1596 | depressive disorder | HGNC:5298 | Homo sapiens (human) | 9177 | HTR3B |
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| DOID:1574 | alcohol use disorder | HGNC:5298 | Homo sapiens (human) | 9177 | HTR3B |
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| DOID:0080930 | primary localized cutaneous amyloidosis 1 | HGNC:8507 | Homo sapiens (human) | 9180 | OSMR |
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| DOID:0080312 | neurodevelopmental disorder with midbrain and hindbrain malformations | HGNC:682 | Homo sapiens (human) | 9181 | ARHGEF2 |
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| DOID:162 | cancer | HGNC:1151 | Homo sapiens (human) | 9184 | BUB3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:0080566 | congenital disorder of glycosylation In | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:162 | cancer | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:0110868 | congenital stationary night blindness 1D | HGNC:10975 | Homo sapiens (human) | 9187 | SLC24A1 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:25132 | Homo sapiens (human) | 91937 | TIMD4 |
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| DOID:0112075 | nuclear type mitochondrial complex I deficiency 10 | HGNC:28086 | Homo sapiens (human) | 91942 | NDUFAF2 |
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| DOID:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:630 | genetic disease | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:0110794 | hereditary spastic paraplegia 42 | HGNC:95 | Homo sapiens (human) | 9197 | SLC33A1 |
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| DOID:1793 | pancreatic cancer | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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| DOID:14323 | Marfan syndrome | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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| DOID:3883 | Lynch syndrome | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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| DOID:4258 | Weissenbacher-Zweymuller syndrome | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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| DOID:0050787 | juvenile polyposis syndrome | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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| DOID:219 | colon cancer | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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| DOID:670 | amphetamine abuse | HGNC:1678 | Homo sapiens (human) | 920 | CD4 |
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