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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:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0050774 | rapadilino syndrome | HGNC:9949 | Homo sapiens (human) | 9401 | RECQL4 |
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| DOID:0112377 | muscular dystrophy-dystroglycanopathy type B14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0111683 | neurofibromatosis-Noonan syndrome | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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| DOID:0080448 | developmental and epileptic encephalopathy 48 | HGNC:567 | Homo sapiens (human) | 8120 | AP3B2 |
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| DOID:0080943 | 46,XX sex reversal 5 | HGNC:7976 | Homo sapiens (human) | 7026 | NR2F2 |
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| DOID:612 | primary immunodeficiency disease | HGNC:25941 | Homo sapiens (human) | 54790 | TET2 |
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| DOID:0111696 | familial adult myoclonic epilepsy 6 | HGNC:11969 | Homo sapiens (human) | 27327 | TNRC6A |
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| DOID:0110989 | Joubert syndrome 20 | HGNC:37234 | Homo sapiens (human) | 79583 | TMEM231 |
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| DOID:0081216 | autosomal recessive intellectual developmental disorder 54 | HGNC:30765 | Homo sapiens (human) | 23043 | TNIK |
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| DOID:0081440 | Peroxisome biogenesis disorder 10B | HGNC:8858 | Homo sapiens (human) | 8504 | PEX3 |
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| DOID:0070526 | PLACK syndrome | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:0080079 | nonsyndromic congenital nail disorder 1 | HGNC:4044 | Homo sapiens (human) | 8323 | FZD6 |
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| DOID:0080348 | Alzheimer's disease 1 | HGNC:7218 | Homo sapiens (human) | 4353 | MPO |
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| DOID:0110749 | type 1 diabetes mellitus 10 | HGNC:6008 | Homo sapiens (human) | 3559 | IL2RA |
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| DOID:0110212 | Charcot-Marie-Tooth disease X-linked recessive 4 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0111247 | hypertension and brachydactyly syndrome | HGNC:8778 | Homo sapiens (human) | 5139 | PDE3A |
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| DOID:9212 | pityriasis rubra pilaris | HGNC:16446 | Homo sapiens (human) | 79092 | CARD14 |
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| DOID:0080754 | X-linked keratosis follicularis spinulosa decalvans | HGNC:15455 | Homo sapiens (human) | 51360 | MBTPS2 |
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| DOID:0111592 | plasminogen deficiency type I | HGNC:9071 | Homo sapiens (human) | 5340 | PLG |
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| DOID:0080728 | Ehlers-Danlos syndrome arthrochalasia type 2 | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0050773 | paraganglioma | HGNC:26034 | Homo sapiens (human) | 54949 | SDHAF2 |
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| DOID:0110136 | Bardet-Biedl syndrome 14 | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0111933 | phosphoglycerate kinase 1 deficiency | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:0081225 | autosomal recessive intellectual developmental disorder 64 | HGNC:21205 | Homo sapiens (human) | 84894 | LINGO1 |
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