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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:14701 | propionic acidemia | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
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| DOID:0060685 | autosomal dominant nocturnal frontal lobe epilepsy 4 | HGNC:1956 | Homo sapiens (human) | 1135 | CHRNA2 |
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| DOID:0110146 | Bartter disease type 4b | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:13533 | osteopetrosis | HGNC:29017 | Homo sapiens (human) | 9842 | PLEKHM1 |
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| DOID:10123 | pigmentation disease | HGNC:6929 | Homo sapiens (human) | 4157 | MC1R |
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| DOID:0080330 | cold-induced sweating syndrome 2 | HGNC:17412 | Homo sapiens (human) | 23529 | CLCF1 |
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| DOID:11830 | myopia | HGNC:26575 | Homo sapiens (human) | 201973 | PRIMPOL |
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| DOID:0110553 | autosomal dominant nonsyndromic deafness 23 | HGNC:10887 | Homo sapiens (human) | 6495 | SIX1 |
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| DOID:0112283 | spondyloepiphyseal dysplasia Kondo-Fu type | HGNC:15456 | Homo sapiens (human) | 8720 | MBTPS1 |
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| DOID:0070095 | oculocutaneous albinism type IB | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:0111998 | immunodeficiency 66 | HGNC:14334 | Homo sapiens (human) | 57591 | MRTFA |
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| DOID:0050589 | inflammatory bowel disease | HGNC:195 | Homo sapiens (human) | 6868 | ADAM17 |
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| DOID:0060936 | dystonia 28 childhood-onset | HGNC:15840 | Homo sapiens (human) | 9757 | KMT2B |
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| DOID:0080290 | familial erythrocytosis 5 | HGNC:3415 | Homo sapiens (human) | 2056 | EPO |
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| DOID:5684 | spondyloepimetaphyseal dysplasia, Sponastrime type | HGNC:7801 | Homo sapiens (human) | 4796 | TONSL |
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| DOID:1324 | lung cancer | HGNC:3236 | Homo sapiens (human) | 1956 | EGFR |
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| DOID:3347 | osteosarcoma | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:0070437 | hyperphosphatasia with impaired intellectual development syndrome 6 | HGNC:28213 | Homo sapiens (human) | 84992 | PIGY |
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| DOID:0070121 | Meckel syndrome 7 | HGNC:7907 | Homo sapiens (human) | 27031 | NPHP3 |
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| DOID:0111773 | 46,XY sex reversal 8 | HGNC:387 | Homo sapiens (human) | 1109 | AKR1C4 |
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| DOID:0110987 | Joubert syndrome 18 | HGNC:24519 | Homo sapiens (human) | 26123 | TCTN3 |
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| DOID:0060256 | Dowling-Degos disease | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:0070384 | developmental and epileptic encephalopathy 98 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:936 | brain disease | HGNC:15594 | Homo sapiens (human) | 51163 | DBR1 |
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| DOID:0111583 | carboxypeptidase N deficiency | HGNC:2312 | Homo sapiens (human) | 1369 | CPN1 |
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