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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 11701 - 11725 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:11204 allergic conjunctivitis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:8766745
DOID:285 hairy cell leukemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:8843970
DOID:2978 carbohydrate metabolic disorder HGNC:8527 Homo sapiens (human) 5019 OXCT1
  • PMID:8844009
DOID:2377 multiple sclerosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:8887999
  • PMID:8964914
  • PMID:9270614
DOID:3892 insulinoma HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:8972754
DOID:28 endocrine system disease MGI:95705 Mus musculus (house mouse) 14595 B4galt1
  • PMID:9013935
DOID:13406 pulmonary sarcoidosis HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:9036208
DOID:653 purine-pyrimidine metabolic disorder HGNC:12563 Homo sapiens (human) 7372 UMPS
  • PMID:9042911
DOID:0060643 primary sclerosing cholangitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9047083
DOID:12549 hepatitis A HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9047083
DOID:2048 autoimmune hepatitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9047083
DOID:4001 ovarian carcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:9066601
DOID:2154 nephroblastoma HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:9070652
DOID:3070 high grade glioma HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:9090379
  • RGD:7240710
DOID:10763 hypertension RGD:2916 Rattus norvegicus (Norway rat) 24506 Ins2
  • PMID:9095092
DOID:11212 hydrophthalmos HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:9097971
DOID:4195 hyperglycemia RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a
  • PMID:9128844
DOID:2871 endometrial carcinoma HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:9221798
DOID:0080365 endometrial hyperplasia HGNC:11755 Homo sapiens (human) 7031 TFF1
  • PMID:9221798
DOID:4947 cholangiocarcinoma HGNC:12541 Homo sapiens (human) 54600 UGT1A9
  • PMID:9230212
DOID:1338 congenital dyserythropoietic anemia MGI:104669 Mus musculus (house mouse) 17158 Man2a1
  • PMID:9230311
DOID:11984 hypertrophic cardiomyopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:9270088
DOID:12930 dilated cardiomyopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:9270088
DOID:783 end stage renal disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:9294834
DOID:0060074 ductal carcinoma in situ HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:9306962

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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