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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:0080325 | tuberous sclerosis 2 | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:12347 | osteogenesis imperfecta | HGNC:26185 | Homo sapiens (human) | 79879 | CCDC134 |
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| DOID:0112372 | Coffin-Siris syndrome 11 | HGNC:11106 | Homo sapiens (human) | 6602 | SMARCD1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:10830 | Homo sapiens (human) | 6455 | SH3GL1 |
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| DOID:0111337 | Jackson-Weiss syndrome | HGNC:3688 | Homo sapiens (human) | 2260 | FGFR1 |
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| DOID:0050580 | hereditary lymphedema | HGNC:16709 | Homo sapiens (human) | 10203 | CALCRL |
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| DOID:0080233 | autosomal dominant intellectual developmental disorder 50 | HGNC:30782 | Homo sapiens (human) | 80155 | NAA15 |
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| DOID:0111840 | Van Esch-O'Driscoll syndrome | HGNC:9173 | Homo sapiens (human) | 5422 | POLA1 |
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| DOID:0080519 | PAPA syndrome | HGNC:9580 | Homo sapiens (human) | 9051 | PSTPIP1 |
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| DOID:0111822 | CHILD syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:4367 | apparent mineralocorticoid excess syndrome | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:0060438 | Cole-Carpenter syndrome | HGNC:8548 | Homo sapiens (human) | 5034 | P4HB |
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| DOID:0070536 | neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0111153 | congenital mirror movement disorder | HGNC:8029 | Homo sapiens (human) | 9423 | NTN1 |
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| DOID:0080948 | agenesis of corpus callosum, cardiac, ocular, and genital syndrome | HGNC:1759 | Homo sapiens (human) | 1000 | CDH2 |
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| DOID:0080868 | primary ovarian insufficiency 11 | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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| DOID:0060682 | autosomal dominant nocturnal frontal lobe epilepsy 1 | HGNC:1958 | Homo sapiens (human) | 1137 | CHRNA4 |
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| DOID:0111632 | familial erythrocytosis 6 | HGNC:4827 | Homo sapiens (human) | 3043 | HBB |
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| DOID:0081118 | benign familial infantile seizures 5 | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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| DOID:0081157 | dilated cardiomyopathy 1LL | HGNC:14000 | Homo sapiens (human) | 63976 | PRDM16 |
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| DOID:0110540 | autosomal recessive nonsyndromic deafness 98 | HGNC:1268 | Homo sapiens (human) | 54084 | TSPEAR |
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| DOID:1024 | leprosy | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:0111422 | familial lipase maturation factor 1 deficiency | HGNC:14154 | Homo sapiens (human) | 64788 | LMF1 |
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| DOID:5844 | myocardial infarction | HGNC:3467 | Homo sapiens (human) | 2099 | ESR1 |
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| DOID:0060688 | arteriovenous malformations of the brain | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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