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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 8201 - 8225 of 12216 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
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:0080140 multiple congenital anomalies-hypotonia-seizures syndrome 3 HGNC:14938 Homo sapiens (human) 51604 PIGT
  • RGD:7240710
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:3125 multiple endocrine neoplasia HGNC:18129 Homo sapiens (human) 51738 GHRL
  • MGI:6194238
DOID:12721 multiple epiphyseal dysplasia FB:FBgn0031850 Drosophila melanogaster (fruit fly) 33941 Tsp CG11326
  • MGI:6194238
DOID:0070303 multiple epiphyseal dysplasia 1 FB:FBgn0031850 Drosophila melanogaster (fruit fly) 33941 Tsp CG11326
  • MGI:6194238
DOID:0070298 multiple epiphyseal dysplasia 2 HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • RGD:7240710
DOID:0070300 multiple epiphyseal dysplasia 4 HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:24598000
  • RGD:7240710
DOID:0070330 multiple mitochondrial dysfunctions syndrome HGNC:4208 Homo sapiens (human) 2653 GCSH
  • RGD:7240710
DOID:9538 multiple myeloma FB:FBgn0004647 Drosophila melanogaster (fruit fly) 31293 N CG3936
  • MGI:6194238
DOID:9538 multiple myeloma HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:7686390
  • PMID:7834632
DOID:9538 multiple myeloma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:22345095
DOID:9538 multiple myeloma MGI:1340899 Mus musculus (house mouse) 12654 Chi3l1
  • MGI:6194238
DOID:9538 multiple myeloma RGD:620874 Rattus norvegicus (Norway rat) 89824 Chi3l1
  • MGI:6194238
DOID:9538 multiple myeloma FB:FBgn0020415 Drosophila melanogaster (fruit fly) 34979 Idgf2 CG4475
  • MGI:6194238
DOID:9538 multiple myeloma HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:29940770
DOID:9538 multiple myeloma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12200397
  • PMID:12815949
DOID:9538 multiple myeloma MGI:98834 Mus musculus (house mouse) 22059 Trp53
  • MGI:6194238
DOID:9538 multiple myeloma FB:FBgn0051072 Drosophila melanogaster (fruit fly) 43223 Lerp CG31072
  • MGI:6194238
DOID:9538 multiple myeloma RGD:2796 Rattus norvegicus (Norway rat) 25058 Hk1
  • 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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