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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:10591 | pre-eclampsia | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:0080988 | pretibial dystrophic epidermolysis bullosa | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:1596 | depressive disorder | HGNC:7941 | Homo sapiens (human) | 4880 | NPPC |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:2097 | Homo sapiens (human) | 1215 | CMA1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:2648 | Homo sapiens (human) | 11283 | CYP4F8 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:10632 | Homo sapiens (human) | 6352 | CCL5 |
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| DOID:0080465 | developmental and epileptic encephalopathy 30 | HGNC:11142 | Homo sapiens (human) | 150094 | SIK1 |
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| DOID:3068 | glioblastoma | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:5082 | liver cirrhosis | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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| DOID:0110014 | age related macular degeneration 1 | HGNC:4888 | Homo sapiens (human) | 3078 | CFHR1 |
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| DOID:3526 | cerebral infarction | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:0081342 | congenital myopathy 8 | HGNC:164 | Homo sapiens (human) | 88 | ACTN2 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:11849 | Homo sapiens (human) | 7098 | TLR3 |
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| DOID:13378 | Kawasaki disease | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:10591 | pre-eclampsia | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:11976 | Homo sapiens (human) | 7148 | TNXB |
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| DOID:0060564 | spinal disease | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:0090109 | autosomal dominant hypocalcemia | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0080621 | glucocorticoid deficiency 1 | HGNC:6930 | Homo sapiens (human) | 4158 | MC2R |
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| DOID:0112010 | pituitary adenoma 3 | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0090082 | hypogonadotropic hypogonadism 20 with or without anosmia | HGNC:3673 | Homo sapiens (human) | 8822 | FGF17 |
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| DOID:0111861 | Meester-Loeys syndrome | HGNC:1044 | Homo sapiens (human) | 633 | BGN |
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| DOID:0110401 | retinitis pigmentosa 74 | HGNC:967 | Homo sapiens (human) | 583 | BBS2 |
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| DOID:0070155 | hereditary sensory and autonomic neuropathy type 2A | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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