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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:11832 | visual epilepsy | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:399 | tuberculosis | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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| DOID:1059 | intellectual disability | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:0080982 | X-linked mental retardation-hypotonic facies syndrome-1 | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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| DOID:0080410 | familial adenomatous polyposis 2 | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:4621 | holoprosencephaly | HGNC:29185 | Homo sapiens (human) | 23007 | PLCH1 |
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| DOID:0050587 | trichotillomania | HGNC:20297 | Homo sapiens (human) | 114798 | SLITRK1 |
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| DOID:3651 | pyruvate carboxylase deficiency disease | HGNC:8636 | Homo sapiens (human) | 5091 | PC |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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| DOID:0111805 | syndromic microphthalmia 6 | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:12361 | Graves' disease | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:8501 | fundus dystrophy | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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| DOID:1883 | hepatitis C | HGNC:4964 | Homo sapiens (human) | 3135 | HLA-G |
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| DOID:8986 | narcolepsy | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0080365 | endometrial hyperplasia | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:612 | primary immunodeficiency disease | HGNC:30227 | Homo sapiens (human) | 84888 | SPPL2A |
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| DOID:10123 | pigmentation disease | HGNC:745 | Homo sapiens (human) | 434 | ASIP |
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| DOID:1070 | primary open angle glaucoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8692 | myeloid leukemia | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:5419 | schizophrenia | HGNC:5232 | Homo sapiens (human) | 3303 | HSPA1A |
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| DOID:0060903 | thrombosis | HGNC:5181 | Homo sapiens (human) | 3273 | HRG |
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| DOID:7147 | ankylosing spondylitis | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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