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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:0070158 | hereditary sensory neuropathy type 1E | HGNC:2976 | Homo sapiens (human) | 1786 | DNMT1 |
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| DOID:0110435 | dilated cardiomyopathy 1GG | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:4396 | Homo sapiens (human) | 2782 | GNB1 |
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| DOID:0070047 | Schuurs-Hoeijmakers Syndrome | HGNC:30032 | Homo sapiens (human) | 55690 | PACS1 |
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| DOID:0080403 | orofacial cleft 10 | HGNC:12502 | Homo sapiens (human) | 7341 | SUMO1 |
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| DOID:10534 | stomach cancer | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:0110677 | congenital myasthenic syndrome 4B | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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| DOID:0050580 | hereditary lymphedema | HGNC:11809 | Homo sapiens (human) | 7075 | TIE1 |
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| DOID:0080557 | congenital disorder of glycosylation Ie | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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| DOID:0070495 | mitochondrial complex IV deficiency nuclear type 8 | HGNC:24316 | Homo sapiens (human) | 51204 | TACO1 |
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| DOID:0111053 | platelet-type bleeding disorder 15 | HGNC:163 | Homo sapiens (human) | 87 | ACTN1 |
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| DOID:12365 | malaria | HGNC:2334 | Homo sapiens (human) | 1378 | CR1 |
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| DOID:0080958 | primary hypoalphalipoproteinemia 2 | HGNC:600 | Homo sapiens (human) | 335 | APOA1 |
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| DOID:0060956 | dystonia 37, early-onset with striatal lesions | HGNC:17359 | Homo sapiens (human) | 53371 | NUP54 |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
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| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:16438 | Homo sapiens (human) | 83959 | SLC4A11 |
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| DOID:3347 | osteosarcoma | HGNC:9884 | Homo sapiens (human) | 5925 | RB1 |
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| DOID:0110805 | hereditary spastic paraplegia 53 | HGNC:24928 | Homo sapiens (human) | 137492 | VPS37A |
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| DOID:10754 | otitis media | HGNC:23336 | Homo sapiens (human) | 144568 | A2ML1 |
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| DOID:0111635 | autosomal recessive nonsyndromic deafness 57 | HGNC:26257 | Homo sapiens (human) | 79955 | PDZD7 |
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| DOID:0112063 | X-Linked immunodeficiency 74 | HGNC:15631 | Homo sapiens (human) | 51284 | TLR7 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:0080239 | autosomal recessive intellectual developmental disorder 61 | HGNC:23625 | Homo sapiens (human) | 9853 | RUSC2 |
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| DOID:0110676 | congenital myasthenic syndrome 13 | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:0070236 | Loeys-Dietz syndrome 5 | HGNC:11769 | Homo sapiens (human) | 7043 | TGFB3 |
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