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 |
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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 |
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DOID:10652 | Alzheimer's disease | HGNC:8023 | Homo sapiens (human) | 4908 | NTF3 |
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DOID:9976 | heroin dependence | HGNC:4087 | Homo sapiens (human) | 2566 | GABRG2 |
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DOID:0080136 | multiple mitochondrial dysfunctions syndrome 4 | HGNC:19857 | Homo sapiens (human) | 122961 | ISCA2 |
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DOID:1580 | diffuse scleroderma | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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DOID:2394 | ovarian cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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DOID:3908 | lung non-small cell carcinoma | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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DOID:10534 | stomach cancer | HGNC:12637 | Homo sapiens (human) | 7403 | KDM6A |
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DOID:6498 | seborrheic keratosis | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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DOID:341 | peripheral vascular disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:9269 | maple syrup urine disease | HGNC:2898 | Homo sapiens (human) | 1738 | DLD |
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DOID:9743 | diabetic neuropathy | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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DOID:0111872 | nonphotosensitive trichothiodystrophy 6 | HGNC:4651 | Homo sapiens (human) | 2961 | GTF2E2 |
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DOID:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | HGNC:24464 | Homo sapiens (human) | 113189 | CHST14 |
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DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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DOID:12849 | autistic disorder | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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DOID:0050908 | myelodysplastic syndrome | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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DOID:1682 | congenital heart disease | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
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DOID:0050908 | myelodysplastic syndrome | HGNC:6973 | Homo sapiens (human) | 4193 | MDM2 |
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DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:25777 | Homo sapiens (human) | 64864 | RFX7 |
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DOID:0060704 | lymphoproliferative syndrome | HGNC:11364 | Homo sapiens (human) | 6774 | STAT3 |
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DOID:3070 | high grade glioma | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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DOID:0050646 | distal arthrogryposis | HGNC:16305 | Homo sapiens (human) | 170689 | ADAMTS15 |
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DOID:0080199 | colorectal carcinoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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DOID:0060468 | Holt-Oram syndrome | HGNC:15924 | Homo sapiens (human) | 57167 | SALL4 |
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DOID:10003 | sensorineural hearing loss | HGNC:4172 | Homo sapiens (human) | 2625 | GATA3 |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024