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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
LM-GlycoRepo
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:0110184 | Charcot-Marie-Tooth disease type 4J | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:9119 | acute myeloid leukemia | HGNC:2348 | Homo sapiens (human) | 1387 | CREBBP |
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| DOID:1407 | anterior uveitis | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:4272 | Homo sapiens (human) | 28964 | GIT1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:281 | Homo sapiens (human) | 150 | ADRA2A |
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| DOID:2841 | asthma | HGNC:10632 | Homo sapiens (human) | 6352 | CCL5 |
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| DOID:0110090 | short-rib thoracic dysplasia 7 with or without polydactyly | HGNC:29250 | Homo sapiens (human) | 57539 | WDR35 |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:3393 | coronary artery disease | HGNC:7176 | Homo sapiens (human) | 4318 | MMP9 |
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| DOID:0090016 | chromosome 5q deletion syndrome | HGNC:10387 | Homo sapiens (human) | 6208 | RPS14 |
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| DOID:0060275 | pontocerebellar hypoplasia type 6 | HGNC:21406 | Homo sapiens (human) | 57038 | RARS2 |
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| DOID:0050633 | ocular albinism 1 | HGNC:20145 | Homo sapiens (human) | 4935 | GPR143 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
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| DOID:3981 | pantothenate kinase-associated neurodegeneration | HGNC:15894 | Homo sapiens (human) | 80025 | PANK2 |
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| DOID:0060212 | amyotrophic lateral sclerosis type 21 | HGNC:6912 | Homo sapiens (human) | 9782 | MATR3 |
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| DOID:0080390 | nephrotic syndrome type 1 | HGNC:7908 | Homo sapiens (human) | 4868 | NPHS1 |
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| DOID:14452 | hypokalemic periodic paralysis | HGNC:1397 | Homo sapiens (human) | 779 | CACNA1S |
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| DOID:14694 | Johanson-Blizzard syndrome | HGNC:16808 | Homo sapiens (human) | 197131 | UBR1 |
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| DOID:0110480 | autosomal recessive nonsyndromic deafness 22 | HGNC:16378 | Homo sapiens (human) | 146183 | OTOA |
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| DOID:9248 | Pallister-Hall syndrome | HGNC:4319 | Homo sapiens (human) | 2737 | GLI3 |
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| DOID:9409 | diabetes insipidus | HGNC:894 | Homo sapiens (human) | 551 | AVP |
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| DOID:850 | lung disease | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0110081 | arrhythmogenic right ventricular dysplasia 10 | HGNC:3049 | Homo sapiens (human) | 1829 | DSG2 |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0112102 | Sotos syndrome 2 | HGNC:7788 | Homo sapiens (human) | 4784 | NFIX |
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