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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:6000 | congestive heart failure | HGNC:11281 | Homo sapiens (human) | 10011 | SRA1 |
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| DOID:0081363 | distal myopathy with rimmed vacuoles | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:0081364 | neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:10763 | hypertension | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:1686 | glaucoma | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:0110068 | frontotemporal dementia and/or amyotrophic lateral sclerosis 3 | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:0081366 | Paget's disease of bone 3 | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:5408 | Paget's disease of bone | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:162 | cancer | HGNC:11279 | Homo sapiens (human) | 6713 | SQLE |
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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: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:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0070152 | hereditary sensory and autonomic neuropathy type 1A | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:0050882 | spinocerebellar ataxia type 5 | HGNC:11276 | Homo sapiens (human) | 6712 | SPTBN2 |
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| DOID:0080058 | autosomal recessive spinocerebellar ataxia 14 | HGNC:11276 | Homo sapiens (human) | 6712 | SPTBN2 |
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| DOID:5572 | Beckwith-Wiedemann syndrome | HGNC:11275 | Homo sapiens (human) | 6711 | SPTBN1 |
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| DOID:0050882 | spinocerebellar ataxia type 5 | HGNC:11275 | Homo sapiens (human) | 6711 | SPTBN1 |
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| DOID:0110917 | hereditary spherocytosis type 2 | HGNC:11274 | Homo sapiens (human) | 6710 | SPTB |
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| DOID:0050882 | spinocerebellar ataxia type 5 | HGNC:11274 | Homo sapiens (human) | 6710 | SPTB |
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| DOID:12971 | hereditary spherocytosis | HGNC:11274 | Homo sapiens (human) | 6710 | SPTB |
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| DOID:0080438 | developmental and epileptic encephalopathy 5 | HGNC:11273 | Homo sapiens (human) | 6709 | SPTAN1 |
|
