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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:12995 | conduct disorder | HGNC:5287 | Homo sapiens (human) | 3351 | HTR1B |
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| DOID:10283 | prostate cancer | HGNC:12669 | Homo sapiens (human) | 7416 | VDAC1 |
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| DOID:0110032 | autosomal dominant Alport syndrome | HGNC:7579 | Homo sapiens (human) | 4627 | MYH9 |
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| DOID:0111932 | severe congenital encephalopathy due to MECP2 mutation | HGNC:6990 | Homo sapiens (human) | 4204 | MECP2 |
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| DOID:627 | severe combined immunodeficiency | HGNC:6024 | Homo sapiens (human) | 3575 | IL7R |
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| DOID:0081312 | T-cell non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:10003 | sensorineural hearing loss | HGNC:7606 | Homo sapiens (human) | 4647 | MYO7A |
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| DOID:2959 | hyperimmunoglobulin syndrome | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
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| DOID:0070337 | epithelial recurrent erosion dystrophy | HGNC:2194 | Homo sapiens (human) | 1308 | COL17A1 |
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| DOID:0112045 | non-syndromic X-linked intellectual disability 93 | HGNC:17342 | Homo sapiens (human) | 254065 | BRWD3 |
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| DOID:0112021 | non-syndromic X-linked intellectual disability ARX-related | HGNC:18060 | Homo sapiens (human) | 170302 | ARX |
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| DOID:0081355 | congenital myopathy 22B | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:446 | primary hyperaldosteronism | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:14040 | autoimmune polyendocrine syndrome | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0050663 | Bethlem myopathy | HGNC:2188 | Homo sapiens (human) | 1303 | COL12A1 |
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| DOID:9562 | primary ciliary dyskinesia | HGNC:12760 | Homo sapiens (human) | 54014 | BRWD1 |
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| DOID:0070394 | developmental and epileptic encephalopathy 108 | HGNC:19036 | Homo sapiens (human) | 23031 | MAST3 |
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| DOID:13378 | Kawasaki disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:10801 | Homo sapiens (human) | 6439 | SFTPB |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0080267 | autosomal dominant nonsyndromic deafness 71 | HGNC:2938 | Homo sapiens (human) | 23312 | DMXL2 |
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| DOID:0112155 | inflammatory bowel disease 29 | HGNC:25599 | Homo sapiens (human) | 55765 | INAVA |
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| DOID:0060211 | amyotrophic lateral sclerosis type 20 | HGNC:5031 | Homo sapiens (human) | 3178 | HNRNPA1 |
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| DOID:0081234 | autosomal recessive intellectual developmental disorder 75 | HGNC:16491 | Homo sapiens (human) | 55367 | PIDD1 |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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