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:0090120 | hereditary neutrophilia | MGI:1339755 | Mus musculus (house mouse) | 12986 | Csf3r |
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DOID:10652 | Alzheimer's disease | HGNC:6692 | Homo sapiens (human) | 4035 | LRP1 |
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DOID:2746 | glycogen storage disease V | HGNC:9726 | Homo sapiens (human) | 5837 | PYGM |
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DOID:0060639 | permanent neonatal diabetes mellitus | MGI:96573 | Mus musculus (house mouse) | 16334 | Ins2 |
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DOID:0050328 | congenital hypothyroidism | HGNC:8622 | Homo sapiens (human) | 7849 | PAX8 |
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DOID:684 | hepatocellular carcinoma | HGNC:11283 | Homo sapiens (human) | 6714 | SRC |
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DOID:6000 | congestive heart failure | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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DOID:0050947 | hereditary hypophosphatemic rickets with hypercalciuria | MGI:1345284 | Mus musculus (house mouse) | 20505 | Slc34a1 |
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DOID:3393 | coronary artery disease | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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DOID:10283 | prostate cancer | RGD:2611 | Rattus norvegicus (Norway rat) | 25022 | Fgfr2 |
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DOID:9970 | obesity | RGD:2289 | Rattus norvegicus (Norway rat) | 24889 | Cckar |
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DOID:2229 | factor XI deficiency | MGI:99481 | Mus musculus (house mouse) | 109821 | F11 |
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DOID:1596 | depressive disorder | HGNC:3023 | Homo sapiens (human) | 1813 | DRD2 |
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DOID:9743 | diabetic neuropathy | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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DOID:10609 | rickets | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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DOID:12716 | newborn respiratory distress syndrome | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
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DOID:0111272 | occipital horn syndrome | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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DOID:850 | lung disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:11759 | hypochromic anemia | RGD:3684 | Rattus norvegicus (Norway rat) | 25715 | Slc11a2 |
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DOID:0060540 | Hermansky-Pudlak syndrome 2 | MGI:1333879 | Mus musculus (house mouse) | 11774 | Ap3b1 |
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DOID:11247 | disseminated intravascular coagulation | RGD:61914 | Rattus norvegicus (Norway rat) | 29436 | Tfpi |
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DOID:0081267 | graft-versus-host disease | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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DOID:1407 | anterior uveitis | RGD:3645 | Rattus norvegicus (Norway rat) | 24770 | Ccl2 |
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DOID:684 | hepatocellular carcinoma | RGD:61888 | Rattus norvegicus (Norway rat) | 58960 | Map2k2 |
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DOID:0090017 | epidermolysis bullosa simplex with muscular dystrophy | MGI:1277961 | Mus musculus (house mouse) | 18810 | Plec |
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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