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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:0110143 | Bartter disease type 2 | HGNC:6255 | Homo sapiens (human) | 3758 | KCNJ1 |
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| DOID:0110376 | retinitis pigmentosa 41 | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
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| DOID:0111160 | camptodactyly-tall stature-scoliosis-hearing loss syndrome | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:4252 | Alexander disease | HGNC:4235 | Homo sapiens (human) | 2670 | GFAP |
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| DOID:0081007 | RNASET2-deficient cystic leukoencephalopathy | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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| DOID:0081301 | intellectual developmental disorder with ocular anomalies and distinctive facial features | HGNC:25094 | Homo sapiens (human) | 92154 | MTSS2 |
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| DOID:0060614 | ulnar-mammary syndrome | HGNC:11602 | Homo sapiens (human) | 6926 | TBX3 |
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| DOID:0050954 | spinocerebellar ataxia type 1 | HGNC:10548 | Homo sapiens (human) | 6310 | ATXN1 |
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| DOID:0111693 | familial adult myoclonic epilepsy 4 | HGNC:25489 | Homo sapiens (human) | 55689 | YEATS2 |
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| DOID:0080109 | infantile myofibromatosis | HGNC:8804 | Homo sapiens (human) | 5159 | PDGFRB |
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| DOID:0060929 | non-syndromic X-linked intellectual developmental disorder 111 | HGNC:13449 | Homo sapiens (human) | 84631 | SLITRK2 |
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| DOID:0112341 | hereditary spastic paraplegia 80 | HGNC:12461 | Homo sapiens (human) | 51271 | UBAP1 |
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| DOID:0110490 | autosomal recessive nonsyndromic deafness 31 | HGNC:16361 | Homo sapiens (human) | 25861 | WHRN |
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| DOID:0110703 | hypotrichosis 6 | HGNC:21307 | Homo sapiens (human) | 147409 | DSG4 |
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| DOID:0080240 | non-syndromic X-linked intellectual disability 106 | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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| DOID:0111072 | myostatin-related muscle hypertrophy | HGNC:4223 | Homo sapiens (human) | 2660 | MSTN |
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| DOID:0090030 | corticosteroid-binding globulin deficiency | HGNC:1540 | Homo sapiens (human) | 866 | SERPINA6 |
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| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | HGNC:30829 | Homo sapiens (human) | 347733 | TUBB2B |
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| DOID:0080991 | congenital myopathy 1B | HGNC:10483 | Homo sapiens (human) | 6261 | RYR1 |
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| DOID:0060812 | syndromic X-linked intellectual disability Siderius type | HGNC:20672 | Homo sapiens (human) | 23133 | PHF8 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | HGNC:7045 | Homo sapiens (human) | 4247 | MGAT2 |
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| DOID:0110766 | hereditary spastic paraplegia 13 | HGNC:5261 | Homo sapiens (human) | 3329 | HSPD1 |
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| DOID:988 | mitral valve prolapse | HGNC:20908 | Homo sapiens (human) | 22873 | DZIP1 |
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| DOID:0111628 | high myopia-sensorineural deafness syndrome | HGNC:23503 | Homo sapiens (human) | 84189 | SLITRK6 |
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| DOID:0111128 | focal segmental glomerulosclerosis 1 | HGNC:166 | Homo sapiens (human) | 81 | ACTN4 |
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