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:0050753 | cerebellar ataxia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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DOID:1432 | blindness | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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DOID:1289 | neurodegenerative disease | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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DOID:2476 | hereditary spastic paraplegia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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DOID:0110657 | congenital myasthenic syndrome 8 | HGNC:329 | Homo sapiens (human) | 375790 | AGRN |
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DOID:9351 | diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:10763 | hypertension | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:11716 | prediabetes syndrome | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:11446 | sciatic neuropathy | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:11832 | visual epilepsy | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:2018 | hyperinsulinism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:1824 | status epilepticus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:0080855 | Parkinsonism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:0111110 | maturity-onset diabetes of the young type 13 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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DOID:206 | hereditary multiple exostoses | FB:FBgn0029175 | Drosophila melanogaster (fruit fly) | 3772101 | sotv | CG8433 |
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DOID:14500 | fucosidosis | FB:FBgn0285958 | Drosophila melanogaster (fruit fly) | 3772574 | Fuca |
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DOID:9744 | type 1 diabetes mellitus | FB:FBgn0285958 | Drosophila melanogaster (fruit fly) | 3772574 | Fuca |
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DOID:8947 | diabetic retinopathy | FB:FBgn0285958 | Drosophila melanogaster (fruit fly) | 3772574 | Fuca |
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DOID:9352 | type 2 diabetes mellitus | FB:FBgn0285958 | Drosophila melanogaster (fruit fly) | 3772574 | Fuca |
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DOID:9351 | diabetes mellitus | FB:FBgn0285958 | Drosophila melanogaster (fruit fly) | 3772574 | Fuca |
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DOID:5212 | congenital disorder of glycosylation | FB:FBgn0011297 | Drosophila melanogaster (fruit fly) | 37754 | Alg3 | CG4084 |
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DOID:0080556 | congenital disorder of glycosylation Id | FB:FBgn0011297 | Drosophila melanogaster (fruit fly) | 37754 | Alg3 | CG4084 |
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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