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:1612 | breast cancer | HGNC:11100 | Homo sapiens (human) | 6597 | SMARCA4 |
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DOID:3672 | rhabdoid cancer | HGNC:11100 | Homo sapiens (human) | 6597 | SMARCA4 |
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DOID:1574 | alcohol use disorder | HGNC:11100 | Homo sapiens (human) | 6597 | SMARCA4 |
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DOID:684 | hepatocellular carcinoma | HGNC:11100 | Homo sapiens (human) | 6597 | SMARCA4 |
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DOID:10283 | prostate cancer | HGNC:11098 | Homo sapiens (human) | 6595 | SMARCA2 |
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DOID:162 | cancer | HGNC:11098 | Homo sapiens (human) | 6595 | SMARCA2 |
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DOID:0081442 | blepharophimosis-impaired intellectual development syndrome | HGNC:11098 | Homo sapiens (human) | 6595 | SMARCA2 |
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DOID:0050340 | opportunistic bacterial infectious disease | HGNC:11098 | Homo sapiens (human) | 6595 | SMARCA2 |
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DOID:1574 | alcohol use disorder | HGNC:11098 | Homo sapiens (human) | 6595 | SMARCA2 |
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DOID:0081441 | Nicolaides-Baraitser syndrome | HGNC:11098 | Homo sapiens (human) | 6595 | SMARCA2 |
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DOID:331 | central nervous system disease | HGNC:11097 | Homo sapiens (human) | 6594 | SMARCA1 |
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DOID:3827 | congenital diaphragmatic hernia | HGNC:11087 | Homo sapiens (human) | 6586 | SLIT3 |
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DOID:9562 | primary ciliary dyskinesia | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:0050144 | Kartagener syndrome | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:0050545 | visceral heterotaxy | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:3827 | congenital diaphragmatic hernia | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:0060224 | atrial fibrillation | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:2975 | cystic kidney disease | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:13207 | proliferative diabetic retinopathy | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:8947 | diabetic retinopathy | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:224 | transient cerebral ischemia | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:0080745 | polymyositis | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:10223 | dermatomyositis | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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DOID:0060825 | Christianson syndrome | HGNC:11079 | Homo sapiens (human) | 10479 | SLC9A6 |
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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