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:10825 | essential hypertension | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:4450 | renal cell carcinoma | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:557 | kidney disease | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:2378 | relapsing-remitting multiple sclerosis | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:0060180 | colitis | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:2527 | nephrosis | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:3021 | acute kidney failure | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:2986 | IgA glomerulonephritis | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:1591 | renovascular hypertension | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:3310 | atopic dermatitis | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:684 | hepatocellular carcinoma | HGNC:17866 | Homo sapiens (human) | 26762 | HAVCR1 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:17869 | Homo sapiens (human) | 27125 | AFF4 |
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DOID:8923 | skin melanoma | HGNC:17869 | Homo sapiens (human) | 27125 | AFF4 |
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DOID:9256 | colorectal cancer | HGNC:17869 | Homo sapiens (human) | 27125 | AFF4 |
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DOID:0111113 | nephronophthisis 2 | HGNC:17870 | Homo sapiens (human) | 27130 | INVS |
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DOID:0060340 | ciliopathy | HGNC:17870 | Homo sapiens (human) | 27130 | INVS |
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DOID:10763 | hypertension | HGNC:17870 | Homo sapiens (human) | 27130 | INVS |
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DOID:6419 | tetralogy of Fallot | HGNC:17870 | Homo sapiens (human) | 27130 | INVS |
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DOID:0070435 | hyperphosphatasia with impaired intellectual development syndrome 3 | HGNC:17893 | Homo sapiens (human) | 27315 | PGAP2 |
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DOID:0050888 | syndromic intellectual disability | HGNC:17896 | Homo sapiens (human) | 27339 | PRPF19 |
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DOID:224 | transient cerebral ischemia | HGNC:17909 | Homo sapiens (human) | 80824 | DUSP16 |
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DOID:9744 | type 1 diabetes mellitus | HGNC:17927 | Homo sapiens (human) | 29843 | SENP1 |
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DOID:1612 | breast cancer | HGNC:17933 | Homo sapiens (human) | 84148 | KAT8 |
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DOID:4467 | clear cell renal cell carcinoma | HGNC:17933 | Homo sapiens (human) | 84148 | KAT8 |
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DOID:1094 | attention deficit hyperactivity disorder | HGNC:17938 | Homo sapiens (human) | 50632 | CALY |
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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 v4.1.1
Last updated: February 17, 2025