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:0050565 | autosomal recessive nonsyndromic deafness | Xenbase:XB-GENE-6488174 | Xenopus laevis (African clawed frog) | 108708472 | tmtc4.L |
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DOID:0050565 | autosomal recessive nonsyndromic deafness | FB:FBgn0038324 | Drosophila melanogaster (fruit fly) | 41867 | Tmtc4 |
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DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:25904 | Homo sapiens (human) | 84899 | TMTC4 |
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DOID:0050565 | autosomal recessive nonsyndromic deafness | ZFIN:ZDB-GENE-070912-148 | Danio rerio (zebrafish) | 560605 | tmtc4 |
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DOID:0050565 | autosomal recessive nonsyndromic deafness | Xenbase:XB-GENE-5771787 | Xenopus tropicalis (tropical clawed frog) | 100158586 | tmtc4 |
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DOID:0110474 | autosomal recessive nonsyndromic deafness 18B | HGNC:8516 | Homo sapiens (human) | 340990 | OTOG |
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DOID:0110474 | autosomal recessive nonsyndromic deafness 18B | MGI:1202064 | Mus musculus (house mouse) | 18419 | Otog |
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DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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DOID:0110480 | autosomal recessive nonsyndromic deafness 22 | HGNC:16378 | Homo sapiens (human) | 146183 | OTOA |
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DOID:0110515 | autosomal recessive nonsyndromic deafness 63 | HGNC:25033 | Homo sapiens (human) | 220074 | LRTOMT |
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DOID:0110530 | autosomal recessive nonsyndromic deafness 84B | MGI:3647600 | Mus musculus (house mouse) | 628870 | Otogl |
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DOID:0110942 | autosomal recessive osteopetrosis 1 | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | RGD:620916 | Rattus norvegicus (Norway rat) | 170911 | Pik3ca |
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DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:20575 | Homo sapiens (human) | 284541 | CYP4A22 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:2642 | Homo sapiens (human) | 1579 | CYP4A11 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | RGD:2081 | Rattus norvegicus (Norway rat) | 24185 | Akt1 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | MGI:87986 | Mus musculus (house mouse) | 11651 | Akt1 |
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DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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DOID:0110861 | autosomal recessive polycystic kidney disease | MGI:1206581 | Mus musculus (house mouse) | 18706 | Pik3ca |
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DOID:4492 | avian influenza | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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DOID:14227 | azoospermia | HGNC:20779 | Homo sapiens (human) | 64579 | NDST4 |
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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