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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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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:0111129 | focal segmental glomerulosclerosis 2 | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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| DOID:0080133 | multiple mitochondrial dysfunctions syndrome 1 | HGNC:16287 | Homo sapiens (human) | 27247 | NFU1 |
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| DOID:0111814 | methylmalonic acidemia and homocysteinemia cblX type | HGNC:4839 | Homo sapiens (human) | 3054 | HCFC1 |
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| DOID:0110500 | autosomal recessive nonsyndromic deafness 42 | HGNC:28741 | Homo sapiens (human) | 286676 | ILDR1 |
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| DOID:0110567 | autosomal dominant nonsyndromic deafness 41 | HGNC:15459 | Homo sapiens (human) | 22953 | P2RX2 |
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| DOID:0110626 | primary ciliary dyskinesia 2 | HGNC:30492 | Homo sapiens (human) | 352909 | DNAAF3 |
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| DOID:13543 | hyperparathyroidism | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0050723 | PSAT deficiency | HGNC:19129 | Homo sapiens (human) | 29968 | PSAT1 |
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| DOID:0080181 | PHARC syndrome | HGNC:15868 | Homo sapiens (human) | 26090 | ABHD12 |
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| DOID:0112207 | developmental and epileptic encephalopathy 71 | HGNC:4331 | Homo sapiens (human) | 2744 | GLS |
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| DOID:0060337 | CEDNIK syndrome | HGNC:11133 | Homo sapiens (human) | 9342 | SNAP29 |
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| DOID:0110377 | retinitis pigmentosa 49 | HGNC:2148 | Homo sapiens (human) | 1259 | CNGA1 |
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| DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:0111580 | Behr syndrome | HGNC:8140 | Homo sapiens (human) | 4976 | OPA1 |
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| DOID:0060728 | NGLY1-deficiency | HGNC:17646 | Homo sapiens (human) | 55768 | NGLY1 |
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| DOID:0080257 | autosomal recessive congenital ichthyosis 13 | HGNC:29958 | Homo sapiens (human) | 121214 | SDR9C7 |
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| DOID:0110436 | dilated cardiomyopathy 1L | HGNC:10807 | Homo sapiens (human) | 6444 | SGCD |
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| DOID:0080141 | mosaic variegated aneuploidy syndrome 1 | HGNC:1149 | Homo sapiens (human) | 701 | BUB1B |
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| DOID:0090145 | dopamine beta-hydroxylase deficiency | HGNC:2689 | Homo sapiens (human) | 1621 | DBH |
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| DOID:0081361 | spastic quadriplegic cerebral palsy 3 | HGNC:245 | Homo sapiens (human) | 120 | ADD3 |
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| DOID:0060649 | congenital hereditary endothelial dystrophy of cornea | HGNC:16438 | Homo sapiens (human) | 83959 | SLC4A11 |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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| DOID:0110456 | dilated cardiomyopathy 1R | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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| DOID:0110713 | Oguchi disease-2 | HGNC:10013 | Homo sapiens (human) | 6011 | GRK1 |
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| DOID:0070332 | multiple mitochondrial dysfunctions syndrome 6 | HGNC:9119 | Homo sapiens (human) | 9512 | PMPCB |
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