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GlyTouCan
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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0050961 | spinocerebellar ataxia type 11 | HGNC:19141 | Homo sapiens (human) | 146057 | TTBK2 |
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| DOID:0080266 | primary ciliary dyskinesia 37 | HGNC:2940 | Homo sapiens (human) | 25981 | DNAH1 |
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| DOID:0110026 | age related macular degeneration 14 | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:0060826 | syndromic X-linked intellectual disability Shashi type | HGNC:9910 | Homo sapiens (human) | 27316 | RBMX |
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| DOID:0050741 | alcohol dependence | HGNC:250 | Homo sapiens (human) | 125 | ADH1B |
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| DOID:0070036 | autosomal dominant intellectual developmental disorder 6 | HGNC:4586 | Homo sapiens (human) | 2904 | GRIN2B |
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| DOID:9206 | Barrett's esophagus | HGNC:18831 | Homo sapiens (human) | 115908 | CTHRC1 |
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| DOID:0070395 | developmental and epileptic encephalopathy 110 | HGNC:1399 | Homo sapiens (human) | 781 | CACNA2D1 |
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| DOID:0081063 | DICER1 syndrome | HGNC:17098 | Homo sapiens (human) | 23405 | DICER1 |
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| DOID:446 | primary hyperaldosteronism | HGNC:1395 | Homo sapiens (human) | 8912 | CACNA1H |
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| DOID:0050489 | multinodular goiter | HGNC:17098 | Homo sapiens (human) | 23405 | DICER1 |
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| DOID:0111981 | immunodeficiency 43 | HGNC:914 | Homo sapiens (human) | 567 | B2M |
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| DOID:0060480 | left ventricular noncompaction | HGNC:3057 | Homo sapiens (human) | 1837 | DTNA |
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| DOID:0110590 | autosomal dominant nonsyndromic deafness 69 | HGNC:6343 | Homo sapiens (human) | 4254 | KITLG |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:6836 | Homo sapiens (human) | 4131 | MAP1B |
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| DOID:0112162 | autosomal recessive nonsyndromic deafness 116 | HGNC:2051 | Homo sapiens (human) | 9080 | CLDN9 |
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| DOID:0080931 | primary localized cutaneous amyloidosis 2 | HGNC:18969 | Homo sapiens (human) | 133396 | IL31RA |
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| DOID:0111834 | X-linked reticulate pigmentary disorder | HGNC:9173 | Homo sapiens (human) | 5422 | POLA1 |
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| DOID:0080218 | primary spontaneous pneumothorax | HGNC:27310 | Homo sapiens (human) | 201163 | FLCN |
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| DOID:0080559 | congenital disorder of glycosylation Ig | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:5585 | Ferguson-Smith tumor | HGNC:11772 | Homo sapiens (human) | 7046 | TGFBR1 |
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| DOID:0080380 | nephrotic syndrome type 5 | HGNC:6487 | Homo sapiens (human) | 3913 | LAMB2 |
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| DOID:0060464 | Feingold syndrome | HGNC:7559 | Homo sapiens (human) | 4613 | MYCN |
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| DOID:0050656 | pseudo-TORCH syndrome 1 | HGNC:8104 | Homo sapiens (human) | 100506658 | OCLN |
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| DOID:10123 | pigmentation disease | HGNC:20820 | Homo sapiens (human) | 219931 | TPCN2 |
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