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:5408 | Paget's disease of bone | HGNC:6079 | Homo sapiens (human) | 3635 | INPP5D |
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DOID:0111843 | Paganini-Miozzo syndrome | HGNC:19133 | Homo sapiens (human) | 90161 | HS6ST2 |
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DOID:0111843 | Paganini-Miozzo syndrome | Xenbase:XB-GENE-6039291 | Xenopus tropicalis (tropical clawed frog) | 100496603 | hs6st2 |
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DOID:0111843 | Paganini-Miozzo syndrome | FB:FBgn0038755 | Drosophila melanogaster (fruit fly) | 42380 | Hs6st | CG4451 |
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DOID:0111843 | Paganini-Miozzo syndrome | RGD:1564397 | Rattus norvegicus (Norway rat) | 302489 | Hs6st2 |
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DOID:0111843 | Paganini-Miozzo syndrome | MGI:1354959 | Mus musculus (house mouse) | 50786 | Hs6st2 |
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DOID:0111843 | Paganini-Miozzo syndrome | ZFIN:ZDB-GENE-030909-14 | Danio rerio (zebrafish) | 378450 | hs6st2 |
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DOID:0080191 | PTEN hamartoma tumor syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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DOID:0111271 | Oliver-McFarlane syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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DOID:1391 | Norum disease | HGNC:6522 | Homo sapiens (human) | 3931 | LCAT |
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DOID:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | SGD:S000000935 | Saccharomyces cerevisiae S288C | 856870 | GLC7 |
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DOID:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | MGI:104871 | Mus musculus (house mouse) | 19046 | Ppp1cb |
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DOID:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | Xenbase:XB-GENE-961670 | Xenopus tropicalis (tropical clawed frog) | 496958 | ppp1cb |
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DOID:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | Xenbase:XB-GENE-17344746 | Xenopus laevis (African clawed frog) | 108717671 | ppp1cb.S |
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DOID:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | RGD:3376 | Rattus norvegicus (Norway rat) | 25594 | Ppp1cb |
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DOID:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | Xenbase:XB-GENE-961676 | Xenopus laevis (African clawed frog) | 443852 | ppp1cb.L |
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DOID:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | HGNC:9282 | Homo sapiens (human) | 5500 | PPP1CB |
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DOID:0080550 | Noonan syndrome with multiple lentigines 3 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:0080550 | Noonan syndrome with multiple lentigines 3 | MGI:88190 | Mus musculus (house mouse) | 109880 | Braf |
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DOID:0060585 | Noonan syndrome 7 | MGI:88190 | Mus musculus (house mouse) | 109880 | Braf |
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DOID:0060585 | Noonan syndrome 7 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:0070113 | Niemann-Pick disease type C1 | MGI:1097712 | Mus musculus (house mouse) | 18145 | Npc1 |
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DOID:0070113 | Niemann-Pick disease type C1 | HGNC:7897 | Homo sapiens (human) | 4864 | NPC1 |
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DOID:0070112 | Niemann-Pick disease type B | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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DOID:0070112 | Niemann-Pick disease type B | WB:WBGene00000211 | Caenorhabditis elegans | 174131 | asm-1 |
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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