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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:9952 | acute lymphoblastic leukemia | HGNC:7652 | Homo sapiens (human) | 4683 | NBN |
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| DOID:0060686 | autosomal dominant nocturnal frontal lobe epilepsy 5 | HGNC:18865 | Homo sapiens (human) | 57582 | KCNT1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:0070478 | diphthamide deficiency syndrome 2 | HGNC:3004 | Homo sapiens (human) | 1802 | DPH2 |
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| DOID:0111526 | Mullerian aplasia and hyperandrogenism | HGNC:12783 | Homo sapiens (human) | 54361 | WNT4 |
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| DOID:0111556 | steatocystoma multiplex | HGNC:6427 | Homo sapiens (human) | 3872 | KRT17 |
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| DOID:0050981 | spinocerebellar ataxia type 34 | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0111892 | Diamond-Blackfan anemia 11 | HGNC:10327 | Homo sapiens (human) | 6154 | RPL26 |
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| DOID:0111571 | Weyers acrofacial dysostosis | HGNC:19747 | Homo sapiens (human) | 132884 | EVC2 |
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| DOID:0110327 | hypertrophic cardiomyopathy 26 | HGNC:3756 | Homo sapiens (human) | 2318 | FLNC |
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| DOID:0111968 | immunodeficiency 41 | HGNC:6008 | Homo sapiens (human) | 3559 | IL2RA |
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| DOID:0112062 | immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia | HGNC:9802 | Homo sapiens (human) | 5880 | RAC2 |
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| DOID:0060717 | autosomal recessive congenital ichthyosis 8 | HGNC:23452 | Homo sapiens (human) | 643418 | LIPN |
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| DOID:0081426 | autosomal recessive distal hereditary motor neuronopathy 7 | HGNC:30910 | Homo sapiens (human) | 64856 | VWA1 |
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| DOID:0081147 | common variable immunodeficiency 4 | HGNC:17755 | Homo sapiens (human) | 115650 | TNFRSF13C |
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| DOID:0110092 | short-rib thoracic dysplasia 6 with or without polydactyly | HGNC:7744 | Homo sapiens (human) | 4750 | NEK1 |
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| DOID:0080730 | Ehlers-Danlos syndrome cardiac valvular type | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0060874 | isolated growth hormone deficiency type IB | HGNC:4266 | Homo sapiens (human) | 2692 | GHRHR |
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| DOID:0060822 | syndromic X-linked intellectual disability Cabezas type | HGNC:2555 | Homo sapiens (human) | 8450 | CUL4B |
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| DOID:0080317 | megalencephalic leukoencephalopathy with subcortical cysts 2B | HGNC:26361 | Homo sapiens (human) | 220296 | HEPACAM |
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| DOID:0050792 | multiple cutaneous and mucosal venous malformations | HGNC:11724 | Homo sapiens (human) | 7010 | TEK |
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| DOID:0090131 | complex cortical dysplasia with other brain malformations | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:0080913 | cerebrooculofacioskeletal syndrome 3 | HGNC:3437 | Homo sapiens (human) | 2073 | ERCC5 |
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| DOID:0111911 | spermatogenic failure 34 | HGNC:21675 | Homo sapiens (human) | 401024 | FSIP2 |
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| DOID:0110705 | hypotrichosis 8 | HGNC:15520 | Homo sapiens (human) | 10161 | LPAR6 |
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