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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:4448 | macular degeneration | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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| DOID:0112019 | non-syndromic X-linked intellectual disability 19 | HGNC:10432 | Homo sapiens (human) | 6197 | RPS6KA3 |
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| DOID:0090080 | hypogonadotropic hypogonadism 16 with or without anosmia | HGNC:10723 | Homo sapiens (human) | 10371 | SEMA3A |
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| DOID:0060939 | dystonia 32 | HGNC:14583 | Homo sapiens (human) | 55823 | VPS11 |
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| DOID:0111631 | familial erythrocytosis 7 | HGNC:4823 | Homo sapiens (human) | 3039 | HBA1 |
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| DOID:0060565 | Ritscher-Schinzel syndrome | HGNC:24641 | Homo sapiens (human) | 57020 | VPS35L |
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| DOID:0111545 | familial male-limited precocious puberty | HGNC:6585 | Homo sapiens (human) | 3973 | LHCGR |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:16980 | Homo sapiens (human) | 10878 | CFHR3 |
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| DOID:4154 | dentinogenesis imperfecta | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:9744 | type 1 diabetes mellitus | RGD:2184 | Rattus norvegicus (Norway rat) | 24221 | Avp |
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| DOID:520 | aortic disease | HGNC:6770 | Homo sapiens (human) | 4089 | SMAD4 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:3121 | gallbladder cancer | HGNC:4317 | Homo sapiens (human) | 2735 | GLI1 |
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| DOID:0112125 | alpha-thalassemia myelodysplasia syndrome | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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| DOID:0110289 | autosomal recessive limb-girdle muscular dystrophy type 2Y | HGNC:29456 | Homo sapiens (human) | 26092 | TOR1AIP1 |
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| DOID:0110414 | retinitis pigmentosa 3 | HGNC:29168 | Homo sapiens (human) | 23322 | RPGRIP1L |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0060244 | specific language impairment | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:2732 | Rothmund-Thomson syndrome | HGNC:19988 | Homo sapiens (human) | 64682 | ANAPC1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:30064 | Homo sapiens (human) | 55193 | PBRM1 |
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| DOID:0112075 | nuclear type mitochondrial complex I deficiency 10 | HGNC:28086 | Homo sapiens (human) | 91942 | NDUFAF2 |
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| DOID:399 | tuberculosis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:1067 | open-angle glaucoma | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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| DOID:1324 | lung cancer | HGNC:15936 | Homo sapiens (human) | 23054 | NCOA6 |
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