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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:0112145 | retinitis pigmentosa 88 | HGNC:15946 | Homo sapiens (human) | 94137 | RP1L1 |
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| DOID:7148 | rheumatoid arthritis | HGNC:18171 | Homo sapiens (human) | 51744 | CD244 |
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| DOID:0081111 | osteosclerotic metaphyseal dysplasia | HGNC:18608 | Homo sapiens (human) | 79705 | LRRK1 |
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| DOID:0080520 | Tn polyagglutination syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:0112040 | non-syndromic X-linked intellectual disability 100 | HGNC:13339 | Homo sapiens (human) | 24137 | KIF4A |
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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:0081151 | common variable immunodeficiency 8 | HGNC:1742 | Homo sapiens (human) | 987 | LRBA |
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| DOID:0110015 | age related macular degeneration 2 | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:0070292 | primary autosomal recessive microcephaly 9 | HGNC:29298 | Homo sapiens (human) | 22995 | CEP152 |
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| DOID:0070287 | primary autosomal recessive microcephaly 11 | HGNC:3182 | Homo sapiens (human) | 1911 | PHC1 |
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| DOID:0110438 | dilated cardiomyopathy 1JJ | HGNC:6484 | Homo sapiens (human) | 3910 | LAMA4 |
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| DOID:0111315 | idiopathic generalized epilepsy 14 | HGNC:13818 | Homo sapiens (human) | 57468 | SLC12A5 |
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| DOID:0112376 | muscular dystrophy-dystroglycanopathy type B15 | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:0060209 | amyotrophic lateral sclerosis type 18 | HGNC:8881 | Homo sapiens (human) | 5216 | PFN1 |
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| DOID:5683 | hereditary breast ovarian cancer syndrome | HGNC:9820 | Homo sapiens (human) | 5889 | RAD51C |
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| DOID:2590 | familial nephrotic syndrome | HGNC:6485 | Homo sapiens (human) | 3911 | LAMA5 |
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| DOID:0110917 | hereditary spherocytosis type 2 | HGNC:11274 | Homo sapiens (human) | 6710 | SPTB |
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| DOID:0112310 | central precocious puberty 1 | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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| DOID:0112378 | muscular dystrophy-dystroglycanopathy type B3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0111202 | autosomal dominant distal hereditary motor neuronopathy 14 | HGNC:2711 | Homo sapiens (human) | 1639 | DCTN1 |
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| DOID:0111481 | combined oxidative phosphorylation deficiency 11 | HGNC:21176 | Homo sapiens (human) | 55005 | RMND1 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:7939 | Homo sapiens (human) | 4878 | NPPA |
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| DOID:0080716 | infantile liver failure syndrome | HGNC:15625 | Homo sapiens (human) | 51594 | NBAS |
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| DOID:0081319 | multiple synostoses syndrome 3 | HGNC:3687 | Homo sapiens (human) | 2254 | FGF9 |
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