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:0080313 | cleft palate-lateral synechia syndrome | MGI:88180 | Mus musculus (house mouse) | 12159 | Bmp4 |
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DOID:0080313 | cleft palate-lateral synechia syndrome | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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DOID:0080313 | cleft palate-lateral synechia syndrome | WB:WBGene00000936 | Caenorhabditis elegans | 179068 | dbl-1 |
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DOID:0080312 | neurodevelopmental disorder with midbrain and hindbrain malformations | MGI:103264 | Mus musculus (house mouse) | 16800 | Arhgef2 |
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DOID:0080312 | neurodevelopmental disorder with midbrain and hindbrain malformations | HGNC:682 | Homo sapiens (human) | 9181 | ARHGEF2 |
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DOID:0080311 | X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance | HGNC:17073 | Homo sapiens (human) | 23092 | ARHGAP26 |
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DOID:0080311 | X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance | MGI:1918552 | Mus musculus (house mouse) | 71302 | Arhgap26 |
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DOID:0080311 | X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance | HGNC:8148 | Homo sapiens (human) | 4983 | OPHN1 |
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DOID:0080309 | fatal infantile hypertonic myofibrillar myopathy | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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DOID:0080309 | fatal infantile hypertonic myofibrillar myopathy | RGD:2414 | Rattus norvegicus (Norway rat) | 25420 | Cryab |
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DOID:0080309 | fatal infantile hypertonic myofibrillar myopathy | MGI:88516 | Mus musculus (house mouse) | 12955 | Cryab |
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DOID:0080301 | atypical hemolytic-uremic syndrome | MGI:1203290 | Mus musculus (house mouse) | 17221 | Cd46 |
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DOID:0080301 | atypical hemolytic-uremic syndrome | MGI:2138169 | Mus musculus (house mouse) | 50702 | Cfhr1 |
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DOID:0080301 | atypical hemolytic-uremic syndrome | MGI:105975 | Mus musculus (house mouse) | 14962 | Cfb |
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DOID:0080301 | atypical hemolytic-uremic syndrome | RGD:2232 | Rattus norvegicus (Norway rat) | 24232 | C3 |
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DOID:0080301 | atypical hemolytic-uremic syndrome | RGD:620429 | Rattus norvegicus (Norway rat) | 79126 | Cfi |
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DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:6953 | Homo sapiens (human) | 4179 | CD46 |
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DOID:0080301 | atypical hemolytic-uremic syndrome | MGI:105937 | Mus musculus (house mouse) | 12630 | Cfi |
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DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:5394 | Homo sapiens (human) | 3426 | CFI |
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DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:4888 | Homo sapiens (human) | 3078 | CFHR1 |
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DOID:0080301 | atypical hemolytic-uremic syndrome | MGI:3646434 | Mus musculus (house mouse) | 214403 | Cfhr4 |
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DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:16980 | Homo sapiens (human) | 10878 | CFHR3 |
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DOID:0080301 | atypical hemolytic-uremic syndrome | MGI:98736 | Mus musculus (house mouse) | 21824 | Thbd |
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DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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DOID:0080301 | atypical hemolytic-uremic syndrome | MGI:88227 | Mus musculus (house mouse) | 12266 | C3 |
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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