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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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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:3512 | neurofibrosarcoma | HGNC:7534 | Homo sapiens (human) | 4601 | MXI1 |
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| DOID:0111434 | optic atrophy 10 | HGNC:18647 | Homo sapiens (human) | 84816 | RTN4IP1 |
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| DOID:12557 | Duane retraction syndrome | HGNC:15924 | Homo sapiens (human) | 57167 | SALL4 |
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| DOID:10584 | retinitis pigmentosa | HGNC:9990 | Homo sapiens (human) | 5995 | RGR |
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| DOID:0060766 | autosomal dominant Robinow syndrome 1 | HGNC:12784 | Homo sapiens (human) | 7474 | WNT5A |
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| DOID:1612 | breast cancer | HGNC:15574 | Homo sapiens (human) | 9821 | RB1CC1 |
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| DOID:5768 | Nager acrofacial dysostosis | HGNC:10771 | Homo sapiens (human) | 10262 | SF3B4 |
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| DOID:11335 | sarcoidosis | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:2187 | amelogenesis imperfecta | HGNC:22140 | Homo sapiens (human) | 56975 | FAM20C |
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| DOID:0070016 | autosomal dominant dyskeratosis congenita 2 | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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| DOID:11383 | cryptorchidism | HGNC:17318 | Homo sapiens (human) | 122042 | RXFP2 |
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| DOID:0050440 | familial partial lipodystrophy | HGNC:281 | Homo sapiens (human) | 150 | ADRA2A |
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| DOID:853 | polymyalgia rheumatica | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:612 | primary immunodeficiency disease | HGNC:16422 | Homo sapiens (human) | 29775 | CARD10 |
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| DOID:4428 | dyslexia | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:0050671 | female breast cancer | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:14115 | toxic shock syndrome | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0090092 | hypogonadotropic hypogonadism 3 with or without anosmia | HGNC:15836 | Homo sapiens (human) | 128674 | PROKR2 |
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| DOID:0060704 | lymphoproliferative syndrome | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:14768 | Saethre-Chotzen syndrome | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:0111039 | hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | HGNC:343 | Homo sapiens (human) | 191 | AHCY |
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| DOID:0081398 | holoprosencephaly 12 | HGNC:7877 | Homo sapiens (human) | 23019 | CNOT1 |
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| DOID:3756 | protein C deficiency | HGNC:9451 | Homo sapiens (human) | 5624 | PROC |
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| DOID:9675 | pulmonary emphysema | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:3526 | cerebral infarction | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
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