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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:0111474 | combined oxidative phosphorylation deficiency 1 | HGNC:13780 | Homo sapiens (human) | 85476 | GFM1 |
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| DOID:0110648 | long QT syndrome 6 | HGNC:6242 | Homo sapiens (human) | 9992 | KCNE2 |
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| DOID:0080263 | autosomal recessive nonsyndromic deafness 108 | HGNC:10256 | Homo sapiens (human) | 4919 | ROR1 |
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| DOID:980 | choroidal sclerosis | HGNC:4689 | Homo sapiens (human) | 3000 | GUCY2D |
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| DOID:0050857 | Perrault syndrome | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:17073 | Homo sapiens (human) | 23092 | ARHGAP26 |
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| DOID:0080893 | Bainbridge-Ropers syndrome | HGNC:29357 | Homo sapiens (human) | 80816 | ASXL3 |
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| DOID:0110876 | holoprosencephaly 7 | HGNC:9585 | Homo sapiens (human) | 5727 | PTCH1 |
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| DOID:1657 | ventricular septal defect | HGNC:4173 | Homo sapiens (human) | 2626 | GATA4 |
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| DOID:3070 | high grade glioma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:0111096 | Fanconi anemia complementation group O | HGNC:9820 | Homo sapiens (human) | 5889 | RAD51C |
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| DOID:0111989 | immunodeficiency 35 | HGNC:12440 | Homo sapiens (human) | 7297 | TYK2 |
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| DOID:0080137 | multiple endocrine neoplasia type 4 | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:0070294 | primary autosomal recessive microcephaly 10 | HGNC:15807 | Homo sapiens (human) | 63925 | ZNF335 |
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| DOID:0111740 | X-linked deafness 6 | HGNC:2208 | Homo sapiens (human) | 1288 | COL4A6 |
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| DOID:0080628 | alopecia-mental retardation syndrome 1 | HGNC:349 | Homo sapiens (human) | 197 | AHSG |
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| DOID:0080382 | nephrotic syndrome type 3 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:4428 | dyslexia | HGNC:21493 | Homo sapiens (human) | 161582 | DNAAF4 |
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| DOID:0112019 | non-syndromic X-linked intellectual disability 19 | HGNC:10432 | Homo sapiens (human) | 6197 | RPS6KA3 |
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| DOID:0090080 | hypogonadotropic hypogonadism 16 with or without anosmia | HGNC:10723 | Homo sapiens (human) | 10371 | SEMA3A |
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| DOID:0060939 | dystonia 32 | HGNC:14583 | Homo sapiens (human) | 55823 | VPS11 |
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| DOID:0111631 | familial erythrocytosis 7 | HGNC:4823 | Homo sapiens (human) | 3039 | HBA1 |
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| DOID:0060565 | Ritscher-Schinzel syndrome | HGNC:24641 | Homo sapiens (human) | 57020 | VPS35L |
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| DOID:0111545 | familial male-limited precocious puberty | HGNC:6585 | Homo sapiens (human) | 3973 | LHCGR |
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| DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:16980 | Homo sapiens (human) | 10878 | CFHR3 |
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