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:6688 | autoimmune lymphoproliferative syndrome | MGI:95484 | Mus musculus (house mouse) | 14102 | Fas |
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DOID:0050947 | hereditary hypophosphatemic rickets with hypercalciuria | MGI:1345284 | Mus musculus (house mouse) | 20505 | Slc34a1 |
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DOID:0112051 | non-syndromic X-linked intellectual disability 30 | MGI:1339656 | Mus musculus (house mouse) | 18481 | Pak3 |
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DOID:13884 | sick sinus syndrome | MGI:98251 | Mus musculus (house mouse) | 20271 | Scn5a |
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DOID:0060849 | osteoporosis-pseudoglioma syndrome | MGI:1278315 | Mus musculus (house mouse) | 16973 | Lrp5 |
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DOID:0111046 | platelet-type bleeding disorder 10 | MGI:107899 | Mus musculus (house mouse) | 12491 | Cd36 |
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DOID:0080351 | CLOVES syndrome | MGI:1206581 | Mus musculus (house mouse) | 18706 | Pik3ca |
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DOID:0110107 | atrial heart septal defect 2 | MGI:95664 | Mus musculus (house mouse) | 14463 | Gata4 |
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DOID:1094 | attention deficit hyperactivity disorder | MGI:2441950 | Mus musculus (house mouse) | 319387 | Adgrl3 |
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DOID:0110336 | osteogenesis imperfecta type 8 | MGI:1888921 | Mus musculus (house mouse) | 56401 | P3h1 |
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DOID:0110030 | alpha thalassemia-X-linked intellectual disability syndrome | MGI:103067 | Mus musculus (house mouse) | 22589 | Atrx |
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DOID:0110862 | congenital stationary night blindness autosomal dominant 1 | MGI:97914 | Mus musculus (house mouse) | 212541 | Rho |
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DOID:0110670 | congenital myasthenic syndrome 9 | MGI:103581 | Mus musculus (house mouse) | 18198 | Musk |
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DOID:9970 | obesity | MGI:97511 | Mus musculus (house mouse) | 18548 | Pcsk1 |
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DOID:13544 | low tension glaucoma | MGI:98351 | Mus musculus (house mouse) | 20655 | Sod1 |
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DOID:14264 | benign neonatal seizures | MGI:1309503 | Mus musculus (house mouse) | 16536 | Kcnq2 |
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DOID:0050473 | Alstrom syndrome | MGI:1934606 | Mus musculus (house mouse) | 236266 | Alms1 |
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DOID:0050659 | biotin-responsive basal ganglia disease | MGI:1931307 | Mus musculus (house mouse) | 80721 | Slc19a3 |
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DOID:0110646 | long QT syndrome 3 | MGI:98251 | Mus musculus (house mouse) | 20271 | Scn5a |
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DOID:0110448 | dilated cardiomyopathy 1HH | MGI:1352493 | Mus musculus (house mouse) | 29810 | Bag3 |
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DOID:0112245 | focal segmental glomerulosclerosis 3 | MGI:1330281 | Mus musculus (house mouse) | 12488 | Cd2ap |
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DOID:0060639 | permanent neonatal diabetes mellitus | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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DOID:14452 | hypokalemic periodic paralysis | MGI:88294 | Mus musculus (house mouse) | 12292 | Cacna1s |
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DOID:0060651 | MYH-9 related disease | MGI:107717 | Mus musculus (house mouse) | 17886 | Myh9 |
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DOID:0080201 | Peters plus syndrome | MGI:2685903 | Mus musculus (house mouse) | 381694 | B3glct |
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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