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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 11251 - 11275 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:0090129 carnitine palmitoyltransferase I deficiency MGI:1098296 Mus musculus (house mouse) 12894 Cpt1a
  • MGI:6194238
  • PMID:16169268
DOID:12351 alcoholic hepatitis RGD:3369 Rattus norvegicus (Norway rat) 25747 Ppara
  • PMID:27939985
DOID:6000 congestive heart failure HGNC:288 Homo sapiens (human) 155 ADRB3
  • MGI:6194238
  • PMID:11273992
DOID:5844 myocardial infarction RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b
  • PMID:16565311
DOID:0080554 congenital disorder of glycosylation Ib MGI:97075 Mus musculus (house mouse) 110119 Mpi
  • MGI:6194238
DOID:0060350 adenine phosphoribosyltransferase deficiency SGD:S000004484 Saccharomyces cerevisiae S288C 854986 APT1
  • MGI:6194238
DOID:206 hereditary multiple exostoses Xenbase:XB-GENE-867525 Xenopus tropicalis (tropical clawed frog) 448393 ext1
  • MGI:6194238
DOID:0110296 autosomal recessive limb-girdle muscular dystrophy type 2M MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus RGD:68396 Rattus norvegicus (Norway rat) 65038 Inppl1
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation Xenbase:XB-GENE-6485822 Xenopus laevis (African clawed frog) 108706812 b4galt1.1.S
  • MGI:6194238
DOID:0060222 Scheie syndrome HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:4195 hyperglycemia HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:17597710
DOID:10223 dermatomyositis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:19953283
DOID:14330 Parkinson's disease HGNC:8999 Homo sapiens (human) 23761 PISD
  • MGI:6194238
DOID:12236 primary biliary cholangitis RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
DOID:2300 spondylolysis HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:26077908
DOID:1459 hypothyroidism RGD:3932 Rattus norvegicus (Norway rat) 54315 Ucp2
  • PMID:21190599
DOID:3371 chondrosarcoma FB:FBgn0064237 Drosophila melanogaster (fruit fly) 37104 Idgf5
  • MGI:6194238
DOID:2741 bilirubin metabolic disorder FB:FBgn0015663 Drosophila melanogaster (fruit fly) 44058 Ugt36A1
  • MGI:6194238
DOID:0014667 disease of metabolism MGI:96572 Mus musculus (house mouse) 16333 Ins1
  • MGI:6194238
DOID:4362 cervical cancer RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:10682 Homo sapiens (human) 6391 SDHC
  • PMID:25576295
DOID:9352 type 2 diabetes mellitus MGI:97370 Mus musculus (house mouse) 18605 Enpp1
  • MGI:6194238
DOID:418 systemic scleroderma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17360781

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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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Last updated: August 19, 2024