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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:0110147 | Bartter disease type 5 | HGNC:16353 | Homo sapiens (human) | 10916 | MAGED2 |
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| DOID:0050591 | tooth agenesis | HGNC:17655 | Homo sapiens (human) | 64388 | GREM2 |
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| DOID:0111479 | combined oxidative phosphorylation deficiency 8 | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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| DOID:0050585 | congenital generalized lipodystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:0080446 | developmental and epileptic encephalopathy 66 | HGNC:23794 | Homo sapiens (human) | 23241 | PACS2 |
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| DOID:0110899 | inflammatory bowel disease 28 | HGNC:5964 | Homo sapiens (human) | 3587 | IL10RA |
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| DOID:0112142 | retinitis pigmentosa 85 | HGNC:348 | Homo sapiens (human) | 196 | AHR |
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| DOID:0080415 | developmental and epileptic encephalopathy 23 | HGNC:19190 | Homo sapiens (human) | 85440 | DOCK7 |
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| DOID:0070154 | hereditary sensory neuropathy type 1F | HGNC:24526 | Homo sapiens (human) | 25923 | ATL3 |
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| DOID:0050742 | nicotine dependence | HGNC:1958 | Homo sapiens (human) | 1137 | CHRNA4 |
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| DOID:0110734 | neurodegeneration with brain iron accumulation | HGNC:2342 | Homo sapiens (human) | 1384 | CRAT |
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| DOID:0070197 | distal myopathy 1 | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
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| DOID:0080237 | autosomal dominant intellectual developmental disorder 46 | HGNC:6299 | Homo sapiens (human) | 56479 | KCNQ5 |
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| DOID:0110591 | autosomal dominant nonsyndromic deafness 7 | HGNC:6653 | Homo sapiens (human) | 4009 | LMX1A |
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| DOID:0110157 | Charcot-Marie-Tooth disease type 2J | HGNC:7225 | Homo sapiens (human) | 4359 | MPZ |
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| DOID:9206 | Barrett's esophagus | HGNC:7376 | Homo sapiens (human) | 4481 | MSR1 |
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| DOID:0111512 | metachondromatosis | HGNC:9644 | Homo sapiens (human) | 5781 | PTPN11 |
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| DOID:0110661 | congenital myasthenic syndrome 20 | HGNC:14025 | Homo sapiens (human) | 60482 | SLC5A7 |
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| DOID:0110814 | hereditary spastic paraplegia 63 | HGNC:469 | Homo sapiens (human) | 271 | AMPD2 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0081373 | disabling pansclerotic morphea | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:0081138 | agammaglobulinemia 6 | HGNC:1699 | Homo sapiens (human) | 974 | CD79B |
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| DOID:10611 | protein-losing enteropathy | HGNC:2665 | Homo sapiens (human) | 1604 | CD55 |
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| DOID:0110645 | long QT syndrome 2 | HGNC:6251 | Homo sapiens (human) | 3757 | KCNH2 |
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| DOID:0060455 | Thiel-Behnke corneal dystrophy | HGNC:11771 | Homo sapiens (human) | 7045 | TGFBI |
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