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:5409 | lung small cell carcinoma | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:2999 | granulosa cell tumor | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:4450 | renal cell carcinoma | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:962 | neurofibroma | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:684 | hepatocellular carcinoma | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:0060669 | cerebral cavernous malformation | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:13207 | proliferative diabetic retinopathy | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:2154 | nephroblastoma | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:1115 | sarcoma | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:11132 | prostatic hypertrophy | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:1289 | neurodegenerative disease | WB:WBGene00010755 | Caenorhabditis elegans | 176441 | vglu-2 |
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DOID:11446 | sciatic neuropathy | WB:WBGene00010755 | Caenorhabditis elegans | 176441 | vglu-2 |
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DOID:0110555 | autosomal dominant nonsyndromic deafness 25 | WB:WBGene00010755 | Caenorhabditis elegans | 176441 | vglu-2 |
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DOID:14330 | Parkinson's disease | WB:WBGene00010755 | Caenorhabditis elegans | 176441 | vglu-2 |
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DOID:224 | transient cerebral ischemia | WB:WBGene00010755 | Caenorhabditis elegans | 176441 | vglu-2 |
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DOID:1289 | neurodegenerative disease | WB:WBGene00011556 | Caenorhabditis elegans | 176442 | vglu-3 |
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DOID:0110555 | autosomal dominant nonsyndromic deafness 25 | WB:WBGene00011556 | Caenorhabditis elegans | 176442 | vglu-3 |
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DOID:11446 | sciatic neuropathy | WB:WBGene00011556 | Caenorhabditis elegans | 176442 | vglu-3 |
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DOID:14330 | Parkinson's disease | WB:WBGene00011556 | Caenorhabditis elegans | 176442 | vglu-3 |
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DOID:224 | transient cerebral ischemia | WB:WBGene00011556 | Caenorhabditis elegans | 176442 | vglu-3 |
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DOID:0112002 | immunodeficiency 47 | WB:WBGene00021952 | Caenorhabditis elegans | 177103 | vha-19 |
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DOID:0070134 | autosomal recessive cutis laxa type IIA | WB:WBGene00006914 | Caenorhabditis elegans | 177626 | vha-5 |
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DOID:14219 | renal tubular acidosis | WB:WBGene00006914 | Caenorhabditis elegans | 177626 | vha-5 |
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DOID:0112171 | wrinkly skin syndrome | WB:WBGene00006914 | Caenorhabditis elegans | 177626 | vha-5 |
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DOID:0110942 | autosomal recessive osteopetrosis 1 | WB:WBGene00006914 | Caenorhabditis elegans | 177626 | vha-5 |
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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