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:12361 | Graves' disease | HGNC:10986 | Homo sapiens (human) | 8034 | SLC25A16 |
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DOID:0110782 | hereditary spastic paraplegia 31 | HGNC:26176 | Homo sapiens (human) | 80346 | REEP4 |
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DOID:0080690 | RASopathy | HGNC:15454 | Homo sapiens (human) | 8036 | SHOC2 |
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DOID:3310 | atopic dermatitis | HGNC:15454 | Homo sapiens (human) | 8036 | SHOC2 |
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DOID:0080692 | Noonan syndrome-like disorder with loose anagen hair 1 | HGNC:15454 | Homo sapiens (human) | 8036 | SHOC2 |
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DOID:0080691 | Noonan syndrome-like disorder with loose anagen hair | HGNC:15454 | Homo sapiens (human) | 8036 | SHOC2 |
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DOID:8398 | osteoarthritis | HGNC:190 | Homo sapiens (human) | 8038 | ADAM12 |
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DOID:2957 | pulmonary tuberculosis | HGNC:18731 | Homo sapiens (human) | 80380 | PDCD1LG2 |
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DOID:1115 | sarcoma | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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DOID:3649 | pyruvate decarboxylase deficiency | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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DOID:0050659 | biotin-responsive basal ganglia disease | HGNC:16266 | Homo sapiens (human) | 80704 | SLC19A3 |
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DOID:784 | chronic kidney disease | HGNC:16266 | Homo sapiens (human) | 80704 | SLC19A3 |
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DOID:0050659 | biotin-responsive basal ganglia disease | MGI:1931307 | Mus musculus (house mouse) | 80721 | Slc19a3 |
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DOID:784 | chronic kidney disease | MGI:1931307 | Mus musculus (house mouse) | 80721 | Slc19a3 |
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DOID:0060251 | sclerosteosis | RGD:69358 | Rattus norvegicus (Norway rat) | 80722 | Sost |
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DOID:0080036 | SOST-related sclerosing bone dysplasia | RGD:69358 | Rattus norvegicus (Norway rat) | 80722 | Sost |
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DOID:0060756 | sclerosteosis 1 | RGD:69358 | Rattus norvegicus (Norway rat) | 80722 | Sost |
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DOID:0080807 | autosomal dominant craniodiaphyseal dysplasia | RGD:69358 | Rattus norvegicus (Norway rat) | 80722 | Sost |
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DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | HGNC:13941 | Homo sapiens (human) | 80736 | SLC44A4 |
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DOID:10003 | sensorineural hearing loss | HGNC:13941 | Homo sapiens (human) | 80736 | SLC44A4 |
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DOID:784 | chronic kidney disease | HGNC:3680 | Homo sapiens (human) | 8074 | FGF23 |
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DOID:0050589 | inflammatory bowel disease | HGNC:3680 | Homo sapiens (human) | 8074 | FGF23 |
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DOID:0050948 | autosomal dominant hypophosphatemic rickets | HGNC:3680 | Homo sapiens (human) | 8074 | FGF23 |
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DOID:4676 | uremia | HGNC:3680 | Homo sapiens (human) | 8074 | FGF23 |
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DOID:2187 | amelogenesis imperfecta | MGI:2136853 | Mus musculus (house mouse) | 80752 | Fam20c |
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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
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024