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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 69051 - 69075 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0090120 hereditary neutrophilia MGI:1339755 Mus musculus (house mouse) 12986 Csf3r
  • MGI:6194238
  • PMID:9639496
DOID:10652 Alzheimer's disease HGNC:6692 Homo sapiens (human) 4035 LRP1
  • MGI:6194238
  • PMID:9635959
DOID:2746 glycogen storage disease V HGNC:9726 Homo sapiens (human) 5837 PYGM
  • MGI:6194238
  • PMID:9633816
  • RGD:7240710
DOID:0060639 permanent neonatal diabetes mellitus MGI:96573 Mus musculus (house mouse) 16334 Ins2
  • MGI:6194238
  • PMID:9593767
DOID:0050328 congenital hypothyroidism HGNC:8622 Homo sapiens (human) 7849 PAX8
  • MGI:6194238
  • PMID:9590296
DOID:684 hepatocellular carcinoma HGNC:11283 Homo sapiens (human) 6714 SRC
  • MGI:6194238
  • PMID:9581679
DOID:6000 congestive heart failure MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
  • PMID:9577949
DOID:0050947 hereditary hypophosphatemic rickets with hypercalciuria MGI:1345284 Mus musculus (house mouse) 20505 Slc34a1
  • MGI:6194238
  • PMID:9560283
DOID:3393 coronary artery disease HGNC:10618 Homo sapiens (human) 6347 CCL2
  • MGI:6194238
  • PMID:9537339
DOID:10283 prostate cancer RGD:2611 Rattus norvegicus (Norway rat) 25022 Fgfr2
  • MGI:6194238
  • PMID:9537256
DOID:9970 obesity RGD:2289 Rattus norvegicus (Norway rat) 24889 Cckar
  • MGI:6194238
  • PMID:9530226
DOID:2229 factor XI deficiency MGI:99481 Mus musculus (house mouse) 109821 F11
  • MGI:6194238
  • PMID:9518045
DOID:1596 depressive disorder HGNC:3023 Homo sapiens (human) 1813 DRD2
  • MGI:6194238
  • PMID:9513185
DOID:9743 diabetic neuropathy HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:9489533
DOID:10609 rickets HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
  • PMID:9486994
DOID:12716 newborn respiratory distress syndrome HGNC:10799 Homo sapiens (human) 729238 SFTPA2
  • MGI:6194238
  • PMID:9475280
DOID:0111272 occipital horn syndrome HGNC:869 Homo sapiens (human) 538 ATP7A
  • MGI:6194238
  • PMID:9467005
  • RGD:7240710
DOID:850 lung disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:9462189
DOID:11759 hypochromic anemia RGD:3684 Rattus norvegicus (Norway rat) 25715 Slc11a2
  • MGI:6194238
  • PMID:9448300
DOID:0060540 Hermansky-Pudlak syndrome 2 MGI:1333879 Mus musculus (house mouse) 11774 Ap3b1
  • MGI:6194238
  • PMID:9434937
DOID:11247 disseminated intravascular coagulation RGD:61914 Rattus norvegicus (Norway rat) 29436 Tfpi
  • MGI:6194238
  • PMID:9426395
DOID:0081267 graft-versus-host disease HGNC:11936 Homo sapiens (human) 356 FASLG
  • MGI:6194238
  • PMID:9404931
DOID:1407 anterior uveitis RGD:3645 Rattus norvegicus (Norway rat) 24770 Ccl2
  • MGI:6194238
  • PMID:9404715
DOID:684 hepatocellular carcinoma RGD:61888 Rattus norvegicus (Norway rat) 58960 Map2k2
  • MGI:6194238
  • PMID:9397988
DOID:0090017 epidermolysis bullosa simplex with muscular dystrophy MGI:1277961 Mus musculus (house mouse) 18810 Plec
  • MGI:6194238
  • PMID:9389647

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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