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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:2349 | arteriosclerosis | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:162 | cancer | HGNC:16467 | Homo sapiens (human) | 9744 | ACAP1 |
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| DOID:0112136 | severe congenital neutropenia 4 | HGNC:24861 | Homo sapiens (human) | 92579 | G6PC3 |
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| DOID:0111997 | immunodeficiency 63 | HGNC:6009 | Homo sapiens (human) | 3560 | IL2RB |
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| DOID:3571 | liver cancer | HGNC:1974 | Homo sapiens (human) | 1147 | CHUK |
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| DOID:9351 | diabetes mellitus | HGNC:5141 | Homo sapiens (human) | 3240 | HP |
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| DOID:7148 | rheumatoid arthritis | HGNC:3374 | Homo sapiens (human) | 2034 | EPAS1 |
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| DOID:784 | chronic kidney disease | HGNC:10524 | Homo sapiens (human) | 6299 | SALL1 |
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| DOID:4751 | striatonigral degeneration | HGNC:8066 | Homo sapiens (human) | 23636 | NUP62 |
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| DOID:0110945 | autosomal recessive osteopetrosis 6 | HGNC:29017 | Homo sapiens (human) | 9842 | PLEKHM1 |
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| DOID:1240 | leukemia | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:2870 | endometrial adenocarcinoma | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:14213 | hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:6543 | acne | HGNC:11917 | Homo sapiens (human) | 7133 | TNFRSF1B |
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| DOID:0111181 | familial hemiplegic migraine 1 | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:1826 | epilepsy | HGNC:17565 | Homo sapiens (human) | 50488 | MINK1 |
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| DOID:4450 | renal cell carcinoma | HGNC:3236 | Homo sapiens (human) | 1956 | EGFR |
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| DOID:0110824 | hereditary spastic paraplegia 9A | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:10763 | hypertension | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:2671 | transitional cell carcinoma | HGNC:600 | Homo sapiens (human) | 335 | APOA1 |
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| DOID:0112358 | short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | HGNC:13655 | Homo sapiens (human) | 222663 | SCUBE3 |
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| DOID:0111668 | Kohlschutter-Tonz syndrome | HGNC:10916 | Homo sapiens (human) | 6561 | SLC13A1 |
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| DOID:9296 | cleft lip | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:299 | adenocarcinoma | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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| DOID:0050451 | Brugada syndrome | HGNC:4634 | Homo sapiens (human) | 2946 | GSTM2 |
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