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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:5408 | Paget's disease of bone | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:403 | Homo sapiens (human) | 224 | ALDH3A2 |
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| DOID:0110868 | congenital stationary night blindness 1D | HGNC:10975 | Homo sapiens (human) | 9187 | SLC24A1 |
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| DOID:0080312 | neurodevelopmental disorder with midbrain and hindbrain malformations | HGNC:682 | Homo sapiens (human) | 9181 | ARHGEF2 |
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| DOID:0110870 | congenital stationary night blindness 1A | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0112247 | congenital heart defects, dysmorphic facial features, and intellectual developmental disorder | HGNC:1733 | Homo sapiens (human) | 8621 | CDK13 |
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| DOID:0080886 | vitamin D-dependent rickets type 1A | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:0110644 | long QT syndrome 1 | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:10024 | Homo sapiens (human) | 6017 | RLBP1 |
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| DOID:9268 | glycine encephalopathy | HGNC:4313 | Homo sapiens (human) | 2731 | GLDC |
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| DOID:0111611 | autosomal recessive spinocerebellar ataxia 4 | HGNC:23595 | Homo sapiens (human) | 55187 | VPS13D |
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| DOID:3770 | pulmonary fibrosis | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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| DOID:0050679 | blue cone monochromacy | HGNC:9936 | Homo sapiens (human) | 5956 | OPN1LW |
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| DOID:0080572 | congenital disorder of glycosylation Iw | HGNC:6172 | Homo sapiens (human) | 3703 | STT3A |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:6501 | Homo sapiens (human) | 3920 | LAMP2 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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| DOID:4989 | pancreatitis | HGNC:9475 | Homo sapiens (human) | 5644 | PRSS1 |
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| DOID:0080336 | mitochondrial DNA depletion syndrome 14 | HGNC:8140 | Homo sapiens (human) | 4976 | OPA1 |
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| DOID:0060001 | withdrawal disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:14330 | Parkinson's disease | HGNC:14581 | Homo sapiens (human) | 65018 | PINK1 |
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| DOID:10763 | hypertension | HGNC:6307 | Homo sapiens (human) | 3791 | KDR |
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| DOID:0070514 | neurodevelopmental disorder with dysmorphic facies and distal limb anomalies | HGNC:3581 | Homo sapiens (human) | 2186 | BPTF |
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| DOID:0050816 | urofacial syndrome | HGNC:18374 | Homo sapiens (human) | 60495 | HPSE2 |
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| DOID:5408 | Paget's disease of bone | HGNC:11908 | Homo sapiens (human) | 8792 | TNFRSF11A |
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| DOID:0110277 | autosomal recessive limb-girdle muscular dystrophy type 2C | HGNC:10809 | Homo sapiens (human) | 6445 | SGCG |
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