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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:3312 | bipolar disorder | HGNC:10934 | Homo sapiens (human) | 6570 | SLC18A1 |
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| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | HGNC:26031 | Homo sapiens (human) | 55650 | PIGV |
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| DOID:11830 | myopia | HGNC:20502 | Homo sapiens (human) | 283375 | SLC39A5 |
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| DOID:10941 | intracranial aneurysm | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:1682 | congenital heart disease | HGNC:3823 | Homo sapiens (human) | 27086 | FOXP1 |
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| DOID:3526 | cerebral infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:14784 | olivopontocerebellar atrophy | HGNC:15984 | Homo sapiens (human) | 54840 | APTX |
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| DOID:1849 | cannabis dependence | HGNC:7997 | Homo sapiens (human) | 3084 | NRG1 |
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| DOID:0080962 | anauxetic dysplasia 2 | HGNC:30129 | Homo sapiens (human) | 10940 | POP1 |
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| DOID:4989 | pancreatitis | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:1586 | rheumatic fever | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0070316 | Miura type epiphyseal chondrodysplasia | HGNC:7944 | Homo sapiens (human) | 4882 | NPR2 |
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| DOID:1883 | hepatitis C | HGNC:18363 | Homo sapiens (human) | 282618 | IFNL1 |
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| DOID:8947 | diabetic retinopathy | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:0111578 | Gillespie syndrome | HGNC:6180 | Homo sapiens (human) | 3708 | ITPR1 |
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| DOID:8986 | narcolepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:0110019 | age related macular degeneration 7 | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:9976 | heroin dependence | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0112214 | developmental and epileptic encephalopathy 78 | HGNC:4076 | Homo sapiens (human) | 2555 | GABRA2 |
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| DOID:0110433 | dilated cardiomyopathy 1E | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0081358 | epidermolytic hyperkeratosis 1 | HGNC:6412 | Homo sapiens (human) | 3848 | KRT1 |
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| DOID:10941 | intracranial aneurysm | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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| DOID:0070277 | primary autosomal recessive microcephaly 15 | HGNC:25897 | Homo sapiens (human) | 84879 | MFSD2A |
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| DOID:10283 | prostate cancer | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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