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:3459 | breast carcinoma | HGNC:1052 | Homo sapiens (human) | 274 | BIN1 |
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DOID:2526 | prostate adenocarcinoma | HGNC:1052 | Homo sapiens (human) | 274 | BIN1 |
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DOID:0111220 | centronuclear myopathy 2 | HGNC:1052 | Homo sapiens (human) | 274 | BIN1 |
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DOID:1925 | Coffin-Siris syndrome | HGNC:21111 | Homo sapiens (human) | 23506 | BICRAL |
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DOID:0112370 | Coffin-Siris syndrome 12 | HGNC:4332 | Homo sapiens (human) | 29998 | BICRA |
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DOID:0050545 | visceral heterotaxy | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
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DOID:2975 | cystic kidney disease | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
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DOID:898 | autosomal dominant polycystic kidney disease | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
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DOID:0111682 | diffuse cystic renal dysplasia | HGNC:19351 | Homo sapiens (human) | 80114 | BICC1 |
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DOID:10534 | stomach cancer | HGNC:1044 | Homo sapiens (human) | 633 | BGN |
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DOID:0112150 | X-linked spondyloepimetaphyseal dysplasia | HGNC:1044 | Homo sapiens (human) | 633 | BGN |
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DOID:0111861 | Meester-Loeys syndrome | HGNC:1044 | Homo sapiens (human) | 633 | BGN |
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DOID:0110264 | cataract 33 | HGNC:1040 | Homo sapiens (human) | 631 | BFSP1 |
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DOID:0111637 | autosomal recessive nonsyndromic deafness 112 | HGNC:13652 | Homo sapiens (human) | 55814 | BDP1 |
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DOID:1679 | cystitis | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:9470 | bacterial meningitis | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:2559 | opiate dependence | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:4483 | rhinitis | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:14330 | Parkinson's disease | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:0050741 | alcohol dependence | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:12894 | Sjogren's syndrome | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:418 | systemic scleroderma | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:12689 | acoustic neuroma | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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DOID:13544 | low tension glaucoma | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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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