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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:11168 | anogenital venereal wart | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:13575 | Homo sapiens (human) | 23476 | BRD4 |
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| DOID:3069 | malignant astrocytoma | HGNC:943 | Homo sapiens (human) | 575 | ADGRB1 |
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| DOID:0050696 | fetal alcohol spectrum disorder | RGD:3075 | Rattus norvegicus (Norway rat) | 29386 | Mecp2 |
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| DOID:0050696 | fetal alcohol spectrum disorder | RGD:2651 | Rattus norvegicus (Norway rat) | 24922 | Gabrb3 |
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| DOID:10652 | Alzheimer's disease | HGNC:9298 | Homo sapiens (human) | 84687 | PPP1R9B |
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| DOID:3069 | malignant astrocytoma | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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| DOID:1682 | congenital heart disease | HGNC:3823 | Homo sapiens (human) | 27086 | FOXP1 |
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| DOID:12577 | urethral obstruction | RGD:3184 | Rattus norvegicus (Norway rat) | 24598 | Nos1 |
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| DOID:0050563 | nonsyndromic deafness | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:0050572 | cone-rod dystrophy | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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| DOID:10283 | prostate cancer | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:6150 | Homo sapiens (human) | 3685 | ITGAV |
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| DOID:9119 | acute myeloid leukemia | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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| DOID:2729 | dyskeratosis congenita | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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| DOID:5082 | liver cirrhosis | HGNC:7553 | Homo sapiens (human) | 4609 | MYC |
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| DOID:3371 | chondrosarcoma | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:1324 | lung cancer | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:8692 | myeloid leukemia | HGNC:8823 | Homo sapiens (human) | 5175 | PECAM1 |
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| DOID:2513 | basal cell carcinoma | HGNC:15762 | Homo sapiens (human) | 51340 | CRNKL1 |
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| DOID:0080188 | chronic myelomonocytic leukemia | HGNC:2439 | Homo sapiens (human) | 1441 | CSF3R |
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| DOID:5773 | oral submucous fibrosis | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:12306 | vitiligo | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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