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:10595 | Charcot-Marie-Tooth disease | HGNC:16825 | Homo sapiens (human) | 55613 | MTMR8 |
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DOID:1459 | hypothyroidism | ZFIN:ZDB-GENE-021031-4 | Danio rerio (zebrafish) | 556077 | plod3 |
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DOID:684 | hepatocellular carcinoma | ZFIN:ZDB-GENE-021031-4 | Danio rerio (zebrafish) | 556077 | plod3 |
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DOID:0060050 | autoimmune disease of blood | ZFIN:ZDB-GENE-060503-810 | Danio rerio (zebrafish) | 555344 | c1galt1a |
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DOID:12140 | Chagas disease | HGNC:9362 | Homo sapiens (human) | 5553 | PRG2 |
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DOID:2841 | asthma | HGNC:9362 | Homo sapiens (human) | 5553 | PRG2 |
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DOID:1725 | peritoneum cancer | HGNC:9362 | Homo sapiens (human) | 5553 | PRG2 |
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DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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DOID:3083 | chronic obstructive pulmonary disease | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:0110339 | osteogenesis imperfecta type 3 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:9675 | pulmonary emphysema | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:12347 | osteogenesis imperfecta | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:6432 | pulmonary hypertension | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:9406 | hypopituitarism | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:224 | transient cerebral ischemia | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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DOID:10763 | hypertension | HGNC:17423 | Homo sapiens (human) | 55501 | CHST12 |
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DOID:10907 | microcephaly | HGNC:24649 | Homo sapiens (human) | 55500 | ETNK1 |
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DOID:10273 | heart conduction disease | HGNC:24649 | Homo sapiens (human) | 55500 | ETNK1 |
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DOID:1826 | epilepsy | HGNC:24649 | Homo sapiens (human) | 55500 | ETNK1 |
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DOID:10763 | hypertension | ZFIN:ZDB-GENE-030131-9885 | Danio rerio (zebrafish) | 553944 | ugcg |
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DOID:14503 | neuronal ceroid lipofuscinosis | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
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DOID:0110721 | neuronal ceroid lipofuscinosis 1 | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
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DOID:0110731 | neuronal ceroid lipofuscinosis 3 | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
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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