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:9452 | steatotic liver disease | RGD:3369 | Rattus norvegicus (Norway rat) | 25747 | Ppara |
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DOID:9452 | steatotic liver disease | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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DOID:783 | end stage renal disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:0090031 | D-bifunctional protein deficiency | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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DOID:1935 | Bardet-Biedl syndrome | HGNC:30000 | Homo sapiens (human) | 27241 | BBS9 |
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DOID:0060747 | Duane-radial ray syndrome | MGI:2139360 | Mus musculus (house mouse) | 99377 | Sall4 |
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DOID:3633 | beta-mannosidosis | MGI:88175 | Mus musculus (house mouse) | 110173 | Manba |
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DOID:10763 | hypertension | RGD:2055 | Rattus norvegicus (Norway rat) | 29412 | Adra1a |
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DOID:10652 | Alzheimer's disease | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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DOID:552 | pneumonia | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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DOID:2843 | long QT syndrome | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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DOID:0050947 | hereditary hypophosphatemic rickets with hypercalciuria | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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DOID:10763 | hypertension | RGD:3717 | Rattus norvegicus (Norway rat) | 29715 | Slc8a1 |
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DOID:6432 | pulmonary hypertension | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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DOID:14330 | Parkinson's disease | HGNC:10935 | Homo sapiens (human) | 6571 | SLC18A2 |
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DOID:0050570 | congenital disorder of glycosylation type I | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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DOID:0110670 | congenital myasthenic syndrome 9 | MGI:103581 | Mus musculus (house mouse) | 18198 | Musk |
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DOID:684 | hepatocellular carcinoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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DOID:5688 | Werner syndrome | MGI:109635 | Mus musculus (house mouse) | 22427 | Wrn |
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DOID:10283 | prostate cancer | HGNC:583 | Homo sapiens (human) | 324 | APC |
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DOID:2349 | arteriosclerosis | RGD:621320 | Rattus norvegicus (Norway rat) | 81687 | Mmp9 |
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DOID:1936 | atherosclerosis | RGD:708418 | Rattus norvegicus (Norway rat) | 84349 | Cd40lg |
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DOID:0060316 | orofaciodigital syndrome I | MGI:1350328 | Mus musculus (house mouse) | 237222 | Ofd1 |
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DOID:3012 | Li-Fraumeni syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:2316 | brain ischemia | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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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