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:0060856 | right atrial isomerism | MGI:106676 | Mus musculus (house mouse) | 22773 | Zic3 |
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DOID:0060856 | right atrial isomerism | HGNC:33983 | Homo sapiens (human) | 653275 | CFC1B |
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DOID:0060856 | right atrial isomerism | RGD:2028 | Rattus norvegicus (Norway rat) | 25366 | Acvr2b |
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DOID:0060856 | right atrial isomerism | WB:WBGene00000900 | Caenorhabditis elegans | 175781 | daf-4 |
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DOID:0060856 | right atrial isomerism | MGI:109448 | Mus musculus (house mouse) | 12627 | Cfc1 |
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DOID:0060855 | autosomal dominant pseudohypoaldosteronism type 1 | HGNC:7979 | Homo sapiens (human) | 4306 | NR3C2 |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | WB:WBGene00000950 | Caenorhabditis elegans | 181035 | deg-1 |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | WB:WBGene00003174 | Caenorhabditis elegans | 181101 | mec-10 |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | RGD:3640 | Rattus norvegicus (Norway rat) | 24767 | Scnn1b |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | MGI:104695 | Mus musculus (house mouse) | 20278 | Scnn1g |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | WB:WBGene00006748 | Caenorhabditis elegans | 177494 | unc-8 |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | WB:WBGene00022815 | Caenorhabditis elegans | 191422 | asic-1 |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | WB:WBGene00006832 | Caenorhabditis elegans | 174306 | unc-105 |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | WB:WBGene00003168 | Caenorhabditis elegans | 181728 | mec-4 |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | MGI:104696 | Mus musculus (house mouse) | 20277 | Scnn1b |
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DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | RGD:3641 | Rattus norvegicus (Norway rat) | 24768 | Scnn1g |
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DOID:0060853 | Potocki-Lupski syndrome | HGNC:9834 | Homo sapiens (human) | 10743 | RAI1 |
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DOID:0060853 | Potocki-Lupski syndrome | MGI:103291 | Mus musculus (house mouse) | 19377 | Rai1 |
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DOID:0060852 | Pierson syndrome | MGI:2387586 | Mus musculus (house mouse) | 209039 | Tns2 |
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DOID:0060852 | Pierson syndrome | HGNC:19737 | Homo sapiens (human) | 23371 | TNS2 |
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DOID:0060852 | Pierson syndrome | HGNC:6487 | Homo sapiens (human) | 3913 | LAMB2 |
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DOID:0060852 | Pierson syndrome | MGI:99916 | Mus musculus (house mouse) | 16779 | Lamb2 |
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DOID:0060852 | Pierson syndrome | FB:FBgn0000244 | Drosophila melanogaster (fruit fly) | 41144 | by |
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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