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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:0111415 | trichohepatoenteric syndrome 1 | HGNC:23639 | Homo sapiens (human) | 9652 | SKIC3 |
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| DOID:612 | primary immunodeficiency disease | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:0060836 | isolated microphthalmia 4 | HGNC:4221 | Homo sapiens (human) | 392255 | GDF6 |
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| DOID:1930 | Laurence-Moon syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0070133 | autosomal recessive cutis laxa type IB | HGNC:3219 | Homo sapiens (human) | 30008 | EFEMP2 |
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| DOID:4465 | papillary renal cell carcinoma | HGNC:9343 | Homo sapiens (human) | 5546 | PRCC |
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| DOID:0050580 | hereditary lymphedema | HGNC:17754 | Homo sapiens (human) | 55901 | THSD1 |
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| DOID:0112242 | congenital symmetric circumferential skin creases 1 | HGNC:20778 | Homo sapiens (human) | 203068 | TUBB |
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| DOID:0111302 | generalized epilepsy with febrile seizures plus 1 | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0111806 | syndromic microphthalmia 5 | HGNC:8522 | Homo sapiens (human) | 5015 | OTX2 |
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| DOID:0050654 | Baller-Gerold syndrome | HGNC:9949 | Homo sapiens (human) | 9401 | RECQL4 |
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| DOID:0050602 | triple-A syndrome | HGNC:13666 | Homo sapiens (human) | 8086 | AAAS |
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| DOID:0111370 | apolipoprotein C-III deficiency | HGNC:610 | Homo sapiens (human) | 345 | APOC3 |
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| DOID:0070282 | primary autosomal recessive microcephaly 8 | HGNC:29086 | Homo sapiens (human) | 9662 | CEP135 |
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| DOID:0081140 | agammaglobulinemia 8A | HGNC:11633 | Homo sapiens (human) | 6929 | TCF3 |
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| DOID:9562 | primary ciliary dyskinesia | HGNC:18661 | Homo sapiens (human) | 56171 | DNAH7 |
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| DOID:0060848 | developmental and epileptic encephalopathy 9 | HGNC:14270 | Homo sapiens (human) | 57526 | PCDH19 |
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| DOID:0111866 | trichothiodystrophy | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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| DOID:2340 | craniosynostosis | HGNC:11623 | Homo sapiens (human) | 6938 | TCF12 |
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| DOID:0070250 | autosomal dominant Emery-Dreifuss muscular dystrophy 5 | HGNC:17084 | Homo sapiens (human) | 23224 | SYNE2 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:17649 | Homo sapiens (human) | 64208 | POPDC3 |
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| DOID:0110539 | autosomal recessive nonsyndromic deafness 97 | HGNC:7029 | Homo sapiens (human) | 4233 | MET |
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| DOID:0090124 | neurogenic-type arthrogryposis multiplex congenita-2 | HGNC:29205 | Homo sapiens (human) | 57222 | ERGIC1 |
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| DOID:0111957 | immunodeficiency 11A | HGNC:16393 | Homo sapiens (human) | 84433 | CARD11 |
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| DOID:0081228 | autosomal recessive intellectual developmental disorder 67 | HGNC:3275 | Homo sapiens (human) | 8665 | EIF3F |
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