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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 69126 - 69150 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:13088 periventricular leukomalacia HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:8652010
DOID:0060350 adenine phosphoribosyltransferase deficiency MGI:88061 Mus musculus (house mouse) 11821 Aprt
  • MGI:6194238
  • PMID:8643571
  • PMID:8864750
DOID:1838 Menkes disease HGNC:6664 Homo sapiens (human) 4015 LOX
  • MGI:6194238
  • PMID:8638917
DOID:2750 glycogen storage disease IV HGNC:4180 Homo sapiens (human) 2632 GBE1
  • MGI:6194238
  • PMID:8613547
  • RGD:7240710
DOID:12308 Dubin-Johnson syndrome RGD:2366 Rattus norvegicus (Norway rat) 25303 Abcc2
  • MGI:6194238
  • PMID:8599091
DOID:3209 junctional epidermolysis bullosa HGNC:6483 Homo sapiens (human) 3909 LAMA3
  • MGI:6194238
  • PMID:8586427
  • RGD:7240710
DOID:11394 adult respiratory distress syndrome RGD:3747 Rattus norvegicus (Norway rat) 24795 Serpina3n
  • MGI:6194238
  • PMID:8574716
DOID:10763 hypertension HGNC:6664 Homo sapiens (human) 4015 LOX
  • MGI:6194238
  • PMID:8562290
DOID:289 endometriosis HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
  • PMID:8550748
DOID:0110666 congenital myasthenic syndrome 3A MGI:87893 Mus musculus (house mouse) 11447 Chrnd
  • MGI:6194238
  • PMID:8538674
DOID:10652 Alzheimer's disease HGNC:15917 Homo sapiens (human) 23236 PLCB1
  • MGI:6194238
  • PMID:8534418
DOID:9352 type 2 diabetes mellitus MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
  • PMID:8530440
DOID:0060870 isolated growth hormone deficiency HGNC:4266 Homo sapiens (human) 2692 GHRHR
  • MGI:6194238
  • PMID:8528260
DOID:0050470 Donohue syndrome MGI:96575 Mus musculus (house mouse) 16337 Insr
  • MGI:6194238
  • PMID:8528241
  • PMID:8612577
DOID:9280 carbamoyl phosphate synthetase I deficiency disease HGNC:2323 Homo sapiens (human) 1373 CPS1
  • MGI:6194238
  • PMID:8486760
  • RGD:7240710
DOID:2750 glycogen storage disease IV SGD:S000000737 Saccharomyces cerevisiae S288C 856705 GLC3
  • MGI:6194238
  • PMID:8463281
DOID:0110339 osteogenesis imperfecta type 3 MGI:88468 Mus musculus (house mouse) 12843 Col1a2
  • MGI:6194238
  • PMID:8446583
  • PMID:8968022
DOID:9252 amino acid metabolic disorder HGNC:5005 Homo sapiens (human) 3155 HMGCL
  • MGI:6194238
  • PMID:8440722
DOID:2861 congenital nonspherocytic hemolytic anemia MGI:95797 Mus musculus (house mouse) 14751 Gpi1
  • MGI:6194238
  • PMID:8417789
DOID:14761 Greig cephalopolysyndactyly syndrome MGI:95729 Mus musculus (house mouse) 14634 Gli3
  • MGI:6194238
  • PMID:8387379
DOID:3310 atopic dermatitis HGNC:6014 Homo sapiens (human) 3565 IL4
  • MGI:6194238
  • PMID:8363440
  • PMID:9643293
DOID:10763 hypertension HGNC:8583 Homo sapiens (human) 5054 SERPINE1
  • MGI:6194238
  • PMID:8355419
DOID:0050427 xeroderma pigmentosum HGNC:12816 Homo sapiens (human) 7508 XPC
  • MGI:6194238
  • PMID:8298653
DOID:11394 adult respiratory distress syndrome HGNC:3176 Homo sapiens (human) 1906 EDN1
  • MGI:6194238
  • PMID:8256914
DOID:2841 asthma HGNC:11526 Homo sapiens (human) 6869 TACR1
  • MGI:6194238
  • PMID:8240667

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

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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