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 | July 29, 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:9266 | cystinuria | SGD:S000003757 | Saccharomyces cerevisiae S288C | 853235 | IMA4 |
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DOID:9266 | cystinuria | SGD:S000003752 | Saccharomyces cerevisiae S288C | 853214 | IMA5 |
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DOID:1059 | intellectual disability | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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DOID:0081221 | autosomal recessive intellectual developmental disorder 59 | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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DOID:3312 | bipolar disorder | HGNC:6051 | Homo sapiens (human) | 3613 | IMPA2 |
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DOID:5419 | schizophrenia | HGNC:6051 | Homo sapiens (human) | 3613 | IMPA2 |
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DOID:5408 | Paget's disease of bone | HGNC:6079 | Homo sapiens (human) | 3635 | INPP5D |
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DOID:9074 | systemic lupus erythematosus | HGNC:6079 | Homo sapiens (human) | 3635 | INPP5D |
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DOID:0110980 | Joubert syndrome 1 | FB:FBgn0036273 | Drosophila melanogaster (fruit fly) | 39404 | INPP5E |
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DOID:0050777 | Joubert syndrome | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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DOID:0050777 | Joubert syndrome | FB:FBgn0036273 | Drosophila melanogaster (fruit fly) | 39404 | INPP5E |
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DOID:9970 | obesity | FB:FBgn0036273 | Drosophila melanogaster (fruit fly) | 39404 | INPP5E |
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DOID:0110980 | Joubert syndrome 1 | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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DOID:9970 | obesity | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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DOID:0080197 | congenital muscular dystrophy with cataracts and intellectual disability | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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DOID:10763 | hypertension | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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DOID:9970 | obesity | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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DOID:11717 | neonatal diabetes | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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DOID:0050524 | maturity-onset diabetes of the young | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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DOID:0110741 | type 1 diabetes mellitus 2 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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DOID:3892 | insulinoma | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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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 v4.0.0
Last updated: August 19, 2024