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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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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:0112125 | alpha-thalassemia myelodysplasia syndrome | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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| DOID:0110289 | autosomal recessive limb-girdle muscular dystrophy type 2Y | HGNC:29456 | Homo sapiens (human) | 26092 | TOR1AIP1 |
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| DOID:2732 | Rothmund-Thomson syndrome | HGNC:19988 | Homo sapiens (human) | 64682 | ANAPC1 |
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| DOID:0112075 | nuclear type mitochondrial complex I deficiency 10 | HGNC:28086 | Homo sapiens (human) | 91942 | NDUFAF2 |
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| DOID:399 | tuberculosis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0111162 | epidermal nevus | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | HGNC:15754 | Homo sapiens (human) | 10398 | MYL9 |
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| DOID:0111773 | 46,XY sex reversal 8 | HGNC:385 | Homo sapiens (human) | 1646 | AKR1C2 |
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| DOID:0070051 | autosomal dominant intellectual developmental disorder 21 | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:0111433 | optic atrophy 3 | HGNC:8142 | Homo sapiens (human) | 80207 | OPA3 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:16639 | Homo sapiens (human) | 23524 | SRRM2 |
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| DOID:2739 | Gilbert syndrome | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0080553 | congenital disorder of glycosylation Iaa | HGNC:21042 | Homo sapiens (human) | 116150 | NUS1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0110223 | Brugada syndrome 6 | HGNC:6243 | Homo sapiens (human) | 10008 | KCNE3 |
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| DOID:0081144 | common variable immunodeficiency 1 | HGNC:5351 | Homo sapiens (human) | 29851 | ICOS |
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| DOID:10908 | hydrocephalus | HGNC:11104 | Homo sapiens (human) | 6599 | SMARCC1 |
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| DOID:0080865 | primary ovarian insufficiency 8 | HGNC:11356 | Homo sapiens (human) | 10734 | STAG3 |
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| DOID:0111680 | essential fructosuria | HGNC:6315 | Homo sapiens (human) | 3795 | KHK |
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| DOID:0070371 | leukoencephalopathy with vanishing white matter 4 | HGNC:3260 | Homo sapiens (human) | 8890 | EIF2B4 |
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| DOID:0110242 | cataract 13 with adult i phenotype | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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| DOID:0110551 | autosomal dominant nonsyndromic deafness 21 | HGNC:13872 | Homo sapiens (human) | 9750 | RIPOR2 |
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| DOID:0080857 | primary ovarian insufficiency 1 | HGNC:3775 | Homo sapiens (human) | 2332 | FMR1 |
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| DOID:0060447 | epithelial basement membrane dystrophy | HGNC:11771 | Homo sapiens (human) | 7045 | TGFBI |
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