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Alliance of Genome Resources

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
Alliance of Genome Resources July 29, 2024
Displaying entries 4001 - 4025 of 12216 in total
Disease ID Disease Name ▼ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9538 multiple myeloma FB:FBgn0020416 Drosophila melanogaster (fruit fly) 34978 Idgf1 CG4472
  • MGI:6194238
DOID:9538 multiple myeloma MGI:96103 Mus musculus (house mouse) 15275 Hk1
  • MGI:6194238
DOID:0070330 multiple mitochondrial dysfunctions syndrome HGNC:4208 Homo sapiens (human) 2653 GCSH
  • RGD:7240710
DOID:0070300 multiple epiphyseal dysplasia 4 HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:24598000
  • RGD:7240710
DOID:0070298 multiple epiphyseal dysplasia 2 HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • RGD:7240710
DOID:0070303 multiple epiphyseal dysplasia 1 FB:FBgn0031850 Drosophila melanogaster (fruit fly) 33941 Tsp CG11326
  • MGI:6194238
DOID:12721 multiple epiphyseal dysplasia FB:FBgn0031850 Drosophila melanogaster (fruit fly) 33941 Tsp CG11326
  • MGI:6194238
DOID:3125 multiple endocrine neoplasia HGNC:18129 Homo sapiens (human) 51738 GHRL
  • MGI:6194238
DOID:0112213 multiple congenital anomalies-hypotonia-seizures syndrome 4 HGNC:14135 Homo sapiens (human) 9091 PIGQ
  • RGD:7240710
DOID:0112213 multiple congenital anomalies-hypotonia-seizures syndrome 4 SGD:S000003448 Saccharomyces cerevisiae S288C 853130 GPI1
  • MGI:6194238
DOID:0080140 multiple congenital anomalies-hypotonia-seizures syndrome 3 HGNC:14938 Homo sapiens (human) 51604 PIGT
  • RGD:7240710
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 ZFIN:ZDB-GENE-040426-1086 Danio rerio (zebrafish) 791759 piga
  • MGI:6194238
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 HGNC:8957 Homo sapiens (human) 5277 PIGA
  • RGD:7240710
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 FB:FBgn0034270 Drosophila melanogaster (fruit fly) 37020 PIG-A
  • MGI:6194238
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 RGD:1589723 Rattus norvegicus (Norway rat) 363464 Piga
  • MGI:6194238
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 MGI:99461 Mus musculus (house mouse) 18700 Piga
  • MGI:6194238
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 Xenbase:XB-GENE-996765 Xenopus tropicalis (tropical clawed frog) 100158632 piga
  • MGI:6194238
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 SGD:S000006096 Saccharomyces cerevisiae S288C 855928 SPT14
  • MGI:6194238
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 WB:WBGene00008431 Caenorhabditis elegans 174386 piga-1
  • MGI:6194238
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 Xenbase:XB-GENE-6485976 Xenopus laevis (African clawed frog) 108707921 piga.L
  • MGI:6194238
DOID:0080138 multiple congenital anomalies-hypotonia-seizures syndrome 1 HGNC:8967 Homo sapiens (human) 23556 PIGN
  • RGD:7240710
DOID:4661 multiple chemical sensitivity HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:23936614
DOID:0050441 mucosulfatidosis HGNC:20376 Homo sapiens (human) 285362 SUMF1
  • MGI:6194238
  • RGD:7240710
DOID:0080178 mucositis MGI:97503 Mus musculus (house mouse) 18538 Pcna
  • MGI:6194238
DOID:0080178 mucositis HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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