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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 3851 - 3875 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:9452 steatotic liver disease MGI:109354 Mus musculus (house mouse) 22228 Ucp2
  • MGI:6194238
DOID:0111103 maturity-onset diabetes of the young type 4 RGD:62387 Rattus norvegicus (Norway rat) 29535 Pdx1
  • MGI:6194238
DOID:10605 short bowel syndrome MGI:104993 Mus musculus (house mouse) 16847 Lepr
  • MGI:6194238
DOID:9884 muscular dystrophy Xenbase:XB-GENE-6489079 Xenopus laevis (African clawed frog) 108698684 pomt2.L
  • MGI:6194238
DOID:583 hemolytic anemia Xenbase:XB-GENE-5962599 Xenopus tropicalis (tropical clawed frog) 549437 abo.3
  • MGI:6194238
DOID:0050642 hypochromic microcytic anemia RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:783 end stage renal disease HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:0080178 mucositis HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:2316 brain ischemia HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:3525 middle cerebral artery infarction HGNC:6783 Homo sapiens (human) 4099 MAG
  • MGI:6194238
DOID:8515 Cor pulmonale RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:8725 vascular dementia RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:0070256 congenital disorder of glycosylation type IId MGI:95705 Mus musculus (house mouse) 14595 B4galt1
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:224 transient cerebral ischemia MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:4762 vasculogenic impotence MGI:88056 Mus musculus (house mouse) 11815 Apod
  • MGI:6194238
DOID:9970 obesity HGNC:9055 Homo sapiens (human) 5330 PLCB2
  • MGI:6194238
DOID:670 amphetamine abuse MGI:88470 Mus musculus (house mouse) 12846 Comt
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma FB:FBgn0064237 Drosophila melanogaster (fruit fly) 37104 Idgf5
  • MGI:6194238
DOID:10763 hypertension SGD:S000002924 Saccharomyces cerevisiae S288C 852128 EMI2
  • MGI:6194238
DOID:2237 hepatitis MGI:2135738 Mus musculus (house mouse) 80908 Abo
  • MGI:6194238
DOID:13550 angle-closure glaucoma HGNC:11743 Homo sapiens (human) 7021 TFAP2B
  • MGI:6194238
DOID:0060462 Desbuquois dysplasia Xenbase:XB-GENE-949402 Xenopus laevis (African clawed frog) 444363 xylt1.L
  • MGI:6194238
DOID:811 lipodystrophy HGNC:13345 Homo sapiens (human) 23175 LPIN1
  • MGI:6194238
DOID:1826 epilepsy HGNC:26899 Homo sapiens (human) 160418 TMTC3
  • 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: August 19, 2024