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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:289 | endometriosis | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:8719 | in situ carcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:0080558 | congenital disorder of glycosylation If | HGNC:7207 | Homo sapiens (human) | 9526 | MPDU1 |
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| DOID:0050889 | non-syndromic intellectual disability | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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| DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:0070157 | hereditary sensory and autonomic neuropathy type 1C | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:8893 | psoriasis | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:0112216 | developmental and epileptic encephalopathy 80 | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
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| DOID:10112 | sleeping sickness | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
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| DOID:0112152 | CHIME syndrome | HGNC:8966 | Homo sapiens (human) | 9487 | PIGL |
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| DOID:5419 | schizophrenia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:2256 | osteochondrodysplasia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:1574 | alcohol use disorder | HGNC:13312 | Homo sapiens (human) | 9446 | GSTO1 |
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| DOID:10652 | Alzheimer's disease | HGNC:13312 | Homo sapiens (human) | 9446 | GSTO1 |
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| DOID:14330 | Parkinson's disease | HGNC:13312 | Homo sapiens (human) | 9446 | GSTO1 |
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| DOID:2043 | hepatitis B | MGI:2137698 | Mus musculus (house mouse) | 94284 | Ugt1a6a |
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| DOID:9352 | type 2 diabetes mellitus | MGI:2137698 | Mus musculus (house mouse) | 94284 | Ugt1a6a |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | RGD:620098 | Rattus norvegicus (Norway rat) | 94273 | Mgat2 |
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| DOID:9743 | diabetic neuropathy | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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| DOID:8947 | diabetic retinopathy | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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| DOID:783 | end stage renal disease | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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