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:11054 | urinary bladder cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:0080562 | congenital disorder of glycosylation Ij | ZFIN:ZDB-GENE-060526-18 | Danio rerio (zebrafish) | 566539 | dpagt1 |
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DOID:479 | angiokeratoma | RGD:1306025 | Rattus norvegicus (Norway rat) | 315165 | Naga |
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DOID:9111 | cutaneous leishmaniasis | MGI:96824 | Mus musculus (house mouse) | 21898 | Tlr4 |
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DOID:2316 | brain ischemia | SGD:S000001568 | Saccharomyces cerevisiae S288C | 853777 | MDH1 |
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DOID:9952 | acute lymphoblastic leukemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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DOID:2738 | pseudoxanthoma elasticum | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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DOID:417 | autoimmune disease | MGI:104803 | Mus musculus (house mouse) | 22619 | Siae |
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DOID:10283 | prostate cancer | RGD:2554 | Rattus norvegicus (Norway rat) | 24334 | Eno2 |
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DOID:219 | colon cancer | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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DOID:0112160 | autosomal dominant nonsyndromic deafness 79 | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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DOID:1485 | cystic fibrosis | RGD:3000 | Rattus norvegicus (Norway rat) | 25608 | Lep |
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DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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DOID:0050730 | coenzyme Q10 deficiency disease | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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DOID:589 | congenital hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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DOID:9744 | type 1 diabetes mellitus | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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DOID:3594 | choriocarcinoma | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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DOID:3454 | brain infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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DOID:13948 | bladder neck obstruction | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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DOID:1312 | focal segmental glomerulosclerosis | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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DOID:5381 | bile duct adenoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:0050570 | congenital disorder of glycosylation type I | RGD:1304826 | Rattus norvegicus (Norway rat) | 315212 | Alg12 |
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DOID:10652 | Alzheimer's disease | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:1287 | cardiovascular system disease | MGI:97370 | Mus musculus (house mouse) | 18605 | Enpp1 |
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DOID:12449 | aplastic anemia | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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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