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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 October 9, 2024
Displaying entries 69576 - 69600 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence Code Names References
DOID:0080046 Stickler syndrome HGNC:2219 Homo sapiens (human) 1299 COL9A3
  • RGD:7240710
DOID:3827 congenital diaphragmatic hernia HGNC:11179 Homo sapiens (human) 6647 SOD1
  • MGI:6194238
DOID:0060072 benign neoplasm HGNC:6515 Homo sapiens (human) 26524 LATS2
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma RGD:2581 Rattus norvegicus (Norway rat) 24890 Esr1
  • MGI:6194238
DOID:684 hepatocellular carcinoma MGI:102496 Mus musculus (house mouse) 17721 ND5
  • MGI:6194238
DOID:1390 hypobetalipoproteinemia RGD:2129 Rattus norvegicus (Norway rat) 54225 Apob
  • MGI:6194238
DOID:0080162 lupus nephritis HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:20538031
DOID:0060041 autism spectrum disorder MGI:1914047 Mus musculus (house mouse) 66797 Cntnap2
  • MGI:6194238
  • PMID:21962519
  • PMID:26647347
DOID:14504 Niemann-Pick disease WB:WBGene00003562 Caenorhabditis elegans 176165 ncr-2
  • MGI:6194238
  • PMID:10801441
  • PMID:15509773
DOID:12894 Sjogren's syndrome HGNC:11929 Homo sapiens (human) 10673 TNFSF13B
  • MGI:6194238
DOID:8398 osteoarthritis HGNC:1076 Homo sapiens (human) 657 BMPR1A
  • MGI:6194238
DOID:5154 borna disease FB:FBgn0023216 Drosophila melanogaster (fruit fly) 31329 Parg
  • MGI:6194238
DOID:12361 Graves' disease WB:WBGene00000898 Caenorhabditis elegans 175410 daf-2
  • MGI:6194238
DOID:0081317 multiple synostoses syndrome 1 RGD:3183 Rattus norvegicus (Norway rat) 25495 Nog
  • MGI:6194238
DOID:9538 multiple myeloma HGNC:4888 Homo sapiens (human) 3078 CFHR1
  • PMID:22348216
DOID:0060180 colitis MGI:98475 Mus musculus (house mouse) 21336 Tacr1
  • MGI:6194238
DOID:0050852 limb ischemia MGI:95407 Mus musculus (house mouse) 13856 Epo
  • MGI:6194238
DOID:11832 visual epilepsy MGI:95753 Mus musculus (house mouse) 14661 Glud1
  • MGI:6194238
DOID:1168 familial hyperlipidemia WB:WBGene00001099 Caenorhabditis elegans 176852 dsc-4
  • MGI:6194238
DOID:5419 schizophrenia MGI:88470 Mus musculus (house mouse) 12846 Comt
  • MGI:6194238
DOID:0060374 orofaciodigital syndrome IV HGNC:24519 Homo sapiens (human) 26123 TCTN3
  • RGD:7240710
DOID:8577 ulcerative colitis RGD:3880 Rattus norvegicus (Norway rat) 25385 Faslg
  • PMID:30122878
DOID:1826 epilepsy FB:FBgn0264975 Drosophila melanogaster (fruit fly) 31792 Nrg
  • PMID:36582832
DOID:10933 obsessive-compulsive disorder HGNC:4232 Homo sapiens (human) 2668 GDNF
  • MGI:6194238
DOID:1168 familial hyperlipidemia RGD:2840 Rattus norvegicus (Norway rat) 24472 Hspa1b
  • 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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Last updated: December 9, 2024