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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
GlycoPOST
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:557 | kidney disease | MGI:1934943 | Mus musculus (house mouse) | 93835 | Amn |
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| DOID:13382 | megaloblastic anemia | MGI:1934943 | Mus musculus (house mouse) | 93835 | Amn |
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| DOID:0050700 | cardiomyopathy | MGI:1934943 | Mus musculus (house mouse) | 93835 | Amn |
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| DOID:9562 | primary ciliary dyskinesia | MGI:1890651 | Mus musculus (house mouse) | 93871 | Brwd1 |
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| DOID:3526 | cerebral infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:3393 | coronary artery disease | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:5844 | myocardial infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:9970 | obesity | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:1287 | cardiovascular system disease | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:10763 | hypertension | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:0060708 | lymphoproliferative syndrome 2 | HGNC:11922 | Homo sapiens (human) | 939 | CD27 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | HGNC:5201 | Homo sapiens (human) | 9394 | HS6ST1 |
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| DOID:1793 | pancreatic cancer | MGI:2136878 | Mus musculus (house mouse) | 93961 | B3galt5 |
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| DOID:4186 | articulation disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:0060038 | specific developmental disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:1470 | major depressive disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:12849 | autistic disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:0111275 | speech-language disorder-1 | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:93 | language disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:5419 | schizophrenia | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:4428 | dyslexia | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:6432 | pulmonary hypertension | HGNC:175 | Homo sapiens (human) | 94 | ACVRL1 |
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| DOID:224 | transient cerebral ischemia | HGNC:175 | Homo sapiens (human) | 94 | ACVRL1 |
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