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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0080665 | warfarin resistance | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:0070382 | developmental and epileptic encephalopathy 95 | HGNC:14937 | Homo sapiens (human) | 94005 | PIGS |
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| DOID:0110196 | Charcot-Marie-Tooth disease type 4G | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:0070259 | congenital disorder of glycosylation type IIg | HGNC:6545 | Homo sapiens (human) | 9382 | COG1 |
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| DOID:0080737 | Ehlers-Danlos syndrome musculocontractural type 2 | HGNC:21144 | Homo sapiens (human) | 29940 | DSE |
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| DOID:0081183 | autosomal recessive intellectual developmental disorder 7 | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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| DOID:0050981 | spinocerebellar ataxia type 34 | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0110980 | Joubert syndrome 1 | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:0080932 | primary localized cutaneous amyloidosis 3 | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:417 | autoimmune disease | HGNC:18187 | Homo sapiens (human) | 54414 | SIAE |
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| DOID:13564 | aspergillosis | HGNC:24355 | Homo sapiens (human) | 51267 | CLEC1A |
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| DOID:0081331 | glycogen storage disease Ic | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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| DOID:0112222 | developmental and epileptic encephalopathy 88 | HGNC:6970 | Homo sapiens (human) | 4190 | MDH1 |
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| DOID:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0112349 | hereditary spastic paraplegia 81 | HGNC:29361 | Homo sapiens (human) | 85465 | SELENOI |
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| DOID:0080459 | developmental and epileptic encephalopathy 12 | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:0110444 | dilated cardiomyopathy 1X | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0112237 | lissencephaly 1 | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:10933 | obsessive-compulsive disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0110961 | atypical Gaucher's disease due to saposin c deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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