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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:0110815 | hereditary spastic paraplegia 64 | HGNC:3363 | Homo sapiens (human) | 953 | ENTPD1 |
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| DOID:0080291 | developmental and epileptic encephalopathy 59 | HGNC:4507 | Homo sapiens (human) | 9568 | GABBR2 |
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| DOID:0070111 | Niemann-Pick disease type A | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:0080986 | Ehlers-Danlos syndrome periodontal type 1 | HGNC:1246 | Homo sapiens (human) | 715 | C1R |
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| DOID:0070254 | congenital disorder of glycosylation type IIb | HGNC:24862 | Homo sapiens (human) | 7841 | MOGS |
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| DOID:0080219 | dystransthyretinemic hyperthyroxinemia | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:0081399 | autosomal dominant distal hereditary motor neuronopathy 10 | HGNC:19880 | Homo sapiens (human) | 11117 | EMILIN1 |
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| DOID:0060827 | X-linked intellectual disability-psychosis-macroorchidism syndrome | HGNC:6990 | Homo sapiens (human) | 4204 | MECP2 |
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| DOID:0070399 | hypomyelinating leukodystrophy 18 | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:4644 | epidermolysis bullosa simplex | HGNC:1090 | Homo sapiens (human) | 667 | DST |
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| DOID:0110665 | congenital myasthenic syndrome 3B | HGNC:1965 | Homo sapiens (human) | 1144 | CHRND |
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| DOID:0111051 | platelet-type bleeding disorder 18 | HGNC:9879 | Homo sapiens (human) | 10235 | RASGRP2 |
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| DOID:0112275 | developmental and epileptic encephalopathy 93 | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:3805 | porokeratosis | HGNC:7530 | Homo sapiens (human) | 4598 | MVK |
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| DOID:0080520 | Tn polyagglutination syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:0050545 | visceral heterotaxy | HGNC:18053 | Homo sapiens (human) | 168507 | PKD1L1 |
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| DOID:0080472 | developmental and epileptic encephalopathy 91 | HGNC:9314 | Homo sapiens (human) | 5530 | PPP3CA |
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| DOID:0080573 | congenital disorder of glycosylation Ix | HGNC:30611 | Homo sapiens (human) | 201595 | STT3B |
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| DOID:0081143 | agammaglobulinemia 8B | HGNC:11633 | Homo sapiens (human) | 6929 | TCF3 |
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| DOID:0111727 | geleophysic dysplasia 3 | HGNC:6716 | Homo sapiens (human) | 4054 | LTBP3 |
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| DOID:0080930 | primary localized cutaneous amyloidosis 1 | HGNC:8507 | Homo sapiens (human) | 9180 | OSMR |
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| DOID:3590 | gestational trophoblastic neoplasm | HGNC:28613 | Homo sapiens (human) | 150365 | MEI1 |
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| DOID:0080414 | developmental and epileptic encephalopathy 15 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:0060193 | amyotrophic lateral sclerosis type 1 | HGNC:7737 | Homo sapiens (human) | 4744 | NEFH |
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| DOID:0110345 | osteogenesis imperfecta type 16 | HGNC:18856 | Homo sapiens (human) | 90993 | CREB3L1 |
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