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:0050431 | arrhythmogenic right ventricular cardiomyopathy | RGD:620314 | Rattus norvegicus (Norway rat) | 689560 | Ryr2 |
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DOID:0060675 | catecholaminergic polymorphic ventricular tachycardia 1 | RGD:620314 | Rattus norvegicus (Norway rat) | 689560 | Ryr2 |
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DOID:1574 | alcohol use disorder | RGD:620314 | Rattus norvegicus (Norway rat) | 689560 | Ryr2 |
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DOID:6000 | congestive heart failure | RGD:620314 | Rattus norvegicus (Norway rat) | 689560 | Ryr2 |
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DOID:6432 | pulmonary hypertension | RGD:620314 | Rattus norvegicus (Norway rat) | 689560 | Ryr2 |
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DOID:8545 | malignant hyperthermia | RGD:620314 | Rattus norvegicus (Norway rat) | 689560 | Ryr2 |
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DOID:11714 | gestational diabetes | RGD:620314 | Rattus norvegicus (Norway rat) | 689560 | Ryr2 |
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DOID:5082 | liver cirrhosis | MGI:1916211 | Mus musculus (house mouse) | 68961 | Phkg2 |
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DOID:2747 | glycogen storage disease | MGI:1916211 | Mus musculus (house mouse) | 68961 | Phkg2 |
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DOID:0111043 | glycogen storage disease IXc | MGI:1916211 | Mus musculus (house mouse) | 68961 | Phkg2 |
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DOID:0111396 | congenital dyserythropoietic anemia type I | MGI:1916218 | Mus musculus (house mouse) | 68968 | Cdan1 |
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DOID:0111398 | congenital dyserythropoietic anemia type Ia | MGI:1916218 | Mus musculus (house mouse) | 68968 | Cdan1 |
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DOID:1338 | congenital dyserythropoietic anemia | MGI:1916218 | Mus musculus (house mouse) | 68968 | Cdan1 |
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DOID:0111870 | nonphotosensitive trichothiodystrophy 7 | HGNC:11572 | Homo sapiens (human) | 6897 | TARS1 |
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DOID:0111867 | nonphotosensitive trichothiodystrophy | HGNC:11572 | Homo sapiens (human) | 6897 | TARS1 |
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DOID:9252 | amino acid metabolic disorder | HGNC:11572 | Homo sapiens (human) | 6897 | TARS1 |
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DOID:0080201 | Peters plus syndrome | RGD:1588723 | Rattus norvegicus (Norway rat) | 689765 | B3glct |
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DOID:0070122 | Meckel syndrome 8 | RGD:1591895 | Rattus norvegicus (Norway rat) | 689779 | Tctn2 |
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DOID:0110993 | Joubert syndrome 24 | RGD:1591895 | Rattus norvegicus (Norway rat) | 689779 | Tctn2 |
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DOID:14227 | azoospermia | MGI:1916231 | Mus musculus (house mouse) | 68981 | Snrpa1 |
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DOID:65 | connective tissue disease | MGI:1916231 | Mus musculus (house mouse) | 68981 | Snrpa1 |
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DOID:5602 | T-cell adult acute lymphocytic leukemia | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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DOID:0111691 | familial adult myoclonic epilepsy 5 | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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DOID:3070 | high grade glioma | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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DOID:850 | lung disease | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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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