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:0070091 | schizophrenia 15 | MGI:1930016 | Mus musculus (house mouse) | 58234 | Shank3 |
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DOID:0070082 | schizophrenia 6 | FB:FBgn0003984 | Drosophila melanogaster (fruit fly) | 38657 | vn |
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DOID:0070082 | schizophrenia 6 | HGNC:7997 | Homo sapiens (human) | 3084 | NRG1 |
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DOID:0070074 | autosomal dominant intellectual developmental disorder 44 | MGI:1927230 | Mus musculus (house mouse) | 223435 | Trio |
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DOID:0070074 | autosomal dominant intellectual developmental disorder 44 | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
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DOID:0070073 | autosomal dominant intellectual developmental disorder 43 | MGI:1338076 | Mus musculus (house mouse) | 15273 | Hivep2 |
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DOID:0070073 | autosomal dominant intellectual developmental disorder 43 | RGD:61988 | Rattus norvegicus (Norway rat) | 29721 | Hivep2 |
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DOID:0070073 | autosomal dominant intellectual developmental disorder 43 | HGNC:4921 | Homo sapiens (human) | 3097 | HIVEP2 |
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DOID:0070072 | autosomal dominant intellectual developmental disorder 42 | MGI:95781 | Mus musculus (house mouse) | 14688 | Gnb1 |
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DOID:0070072 | autosomal dominant intellectual developmental disorder 42 | HGNC:4396 | Homo sapiens (human) | 2782 | GNB1 |
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DOID:0070070 | autosomal dominant intellectual developmental disorder 40 | MGI:1196398 | Mus musculus (house mouse) | 101994 | Champ1 |
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DOID:0070070 | autosomal dominant intellectual developmental disorder 40 | HGNC:20311 | Homo sapiens (human) | 283489 | CHAMP1 |
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DOID:0070069 | autosomal dominant intellectual developmental disorder 39 | MGI:1100511 | Mus musculus (house mouse) | 17933 | Myt1l |
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DOID:0070068 | autosomal dominant intellectual developmental disorder 38 | HGNC:3192 | Homo sapiens (human) | 1917 | EEF1A2 |
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DOID:0070068 | autosomal dominant intellectual developmental disorder 38 | MGI:1096317 | Mus musculus (house mouse) | 13628 | Eef1a2 |
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DOID:0070068 | autosomal dominant intellectual developmental disorder 38 | WB:WBGene00001169 | Caenorhabditis elegans | 181044 | eef-1A.2 |
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DOID:0070068 | autosomal dominant intellectual developmental disorder 38 | WB:WBGene00001168 | Caenorhabditis elegans | 175975 | eef-1A.1 |
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DOID:0070067 | White-Sutton syndrome | HGNC:18801 | Homo sapiens (human) | 23126 | POGZ |
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DOID:0070067 | White-Sutton syndrome | MGI:2442117 | Mus musculus (house mouse) | 229584 | Pogz |
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DOID:0070067 | White-Sutton syndrome | RGD:1309980 | Rattus norvegicus (Norway rat) | 310658 | Pogz |
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DOID:0070066 | autosomal dominant intellectual developmental disorder 36 | HGNC:9302 | Homo sapiens (human) | 5518 | PPP2R1A |
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DOID:0070065 | autosomal dominant intellectual developmental disorder 35 | HGNC:9312 | Homo sapiens (human) | 5528 | PPP2R5D |
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DOID:0070063 | autosomal dominant intellectual developmental disorder 33 | SGD:S000005745 | Saccharomyces cerevisiae S288C | 854394 | STE13 |
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DOID:0070063 | autosomal dominant intellectual developmental disorder 33 | WB:WBGene00001054 | Caenorhabditis elegans | 180042 | dpf-1 |
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DOID:0070063 | autosomal dominant intellectual developmental disorder 33 | HGNC:3010 | Homo sapiens (human) | 1804 | DPP6 |
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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