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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070157 | hereditary sensory and autonomic neuropathy type 1C | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:8893 | psoriasis | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:162 | cancer | HGNC:11279 | Homo sapiens (human) | 6713 | SQLE |
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| DOID:9970 | obesity | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:10283 | prostate cancer | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:1459 | hypothyroidism | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:3459 | breast carcinoma | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:11132 | prostatic hypertrophy | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:12700 | hyperprolactinemia | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:12700 | hyperprolactinemia | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:9351 | diabetes mellitus | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:10283 | prostate cancer | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:10892 | hypospadias | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:3459 | breast carcinoma | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:1380 | endometrial cancer | HGNC:11377 | Homo sapiens (human) | 6783 | SULT1E1 |
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| DOID:1612 | breast cancer | HGNC:11377 | Homo sapiens (human) | 6783 | SULT1E1 |
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| DOID:1700 | X-linked ichthyosis | HGNC:11425 | Homo sapiens (human) | 412 | STS |
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| DOID:10763 | hypertension | HGNC:11425 | Homo sapiens (human) | 412 | STS |
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| DOID:11383 | cryptorchidism | HGNC:11425 | Homo sapiens (human) | 412 | STS |
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| DOID:0080124 | mitochondrial DNA depletion syndrome 5 | HGNC:11448 | Homo sapiens (human) | 8803 | SUCLA2 |
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| DOID:0080128 | mitochondrial DNA depletion syndrome 9 | HGNC:11449 | Homo sapiens (human) | 8802 | SUCLG1 |
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| DOID:0080258 | autosomal recessive congenital ichthyosis 14 | HGNC:11459 | Homo sapiens (human) | 6820 | SULT2B1 |
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| DOID:14250 | Down syndrome | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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