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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:12849 | autistic disorder | HGNC:18541 | Homo sapiens (human) | 55904 | KMT2E |
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| DOID:1883 | hepatitis C | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
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| DOID:3145 | hyperlipoproteinemia type III | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:11981 | morbid obesity | HGNC:4479 | Homo sapiens (human) | 2847 | MCHR1 |
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| DOID:705 | Leber hereditary optic neuropathy | HGNC:7461 | Homo sapiens (human) | 4540 | MT-ND5 |
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| DOID:0081124 | craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1 | HGNC:18188 | Homo sapiens (human) | 54499 | TMCO1 |
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| DOID:2893 | cervix carcinoma | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:4947 | cholangiocarcinoma | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:3382 | liposarcoma | HGNC:4010 | Homo sapiens (human) | 2521 | FUS |
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| DOID:5419 | schizophrenia | HGNC:6700 | Homo sapiens (human) | 7804 | LRP8 |
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| DOID:2921 | glomerulonephritis | HGNC:1241 | Homo sapiens (human) | 712 | C1QA |
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| DOID:0060645 | chronic recurrent multifocal osteomyelitis | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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| DOID:2048 | autoimmune hepatitis | HGNC:4940 | Homo sapiens (human) | 3115 | HLA-DPB1 |
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| DOID:0111210 | autosomal dominant distal hereditary motor neuronopathy 6 | HGNC:28844 | Homo sapiens (human) | 81545 | FBXO38 |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:33914 | Homo sapiens (human) | 100127206 | MINAR2 |
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| DOID:0080160 | Cytomegalovirus retinitis | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:0112263 | hypoinsulinemic hypoglycemia with hemihypertrophy | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:0110976 | brachydactyly type E2 | HGNC:9607 | Homo sapiens (human) | 5744 | PTHLH |
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| DOID:3307 | teratoma | HGNC:7850 | Homo sapiens (human) | 4831 | NME2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:0111353 | arthrogryposis, renal dysfunction, and cholestasis 1 | HGNC:12712 | Homo sapiens (human) | 26276 | VPS33B |
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| DOID:13141 | uveitis | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:5409 | lung small cell carcinoma | HGNC:172 | Homo sapiens (human) | 91 | ACVR1B |
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| DOID:4621 | holoprosencephaly | HGNC:9585 | Homo sapiens (human) | 5727 | PTCH1 |
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