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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 126 - 150 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0050811 congenital adrenal hyperplasia HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
  • PMID:1430088
  • PMID:8964882
DOID:2671 transitional cell carcinoma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • MGI:6194238
  • PMID:14499677
DOID:9970 obesity MGI:104963 Mus musculus (house mouse) 18166 Npy1r
  • MGI:6194238
  • PMID:14525913
DOID:9452 steatotic liver disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
  • PMID:14606109
DOID:0050663 Bethlem myopathy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
  • PMID:14625552
  • PMID:9817932
DOID:0110635 muscular dystrophy-dystroglycanopathy type B5 HGNC:17997 Homo sapiens (human) 79147 FKRP
  • MGI:6194238
  • PMID:14652796
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus MGI:96545 Mus musculus (house mouse) 16177 Il1r1
  • MGI:6194238
  • PMID:14693705
DOID:9743 diabetic neuropathy HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
  • PMID:14693986
DOID:9273 citrullinemia MGI:1354721 Mus musculus (house mouse) 50799 Slc25a13
  • MGI:6194238
  • PMID:14701727
DOID:10763 hypertension RGD:2379 Rattus norvegicus (Norway rat) 24267 Comt
  • MGI:6194238
  • PMID:14714585
  • PMID:17510509
  • PMID:17978496
DOID:3323 Sandhoff disease MGI:96074 Mus musculus (house mouse) 15212 Hexb
  • MGI:6194238
  • PMID:14722612
  • PMID:23028353
  • PMID:31547903
  • PMID:7550345
  • PMID:8789434
DOID:3328 temporal lobe epilepsy HGNC:4341 Homo sapiens (human) 2752 GLUL
  • MGI:6194238
  • PMID:14723991
DOID:5419 schizophrenia HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
  • PMID:14745448
  • PMID:15254796
  • PMID:16397405
DOID:5419 schizophrenia HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:14745448
  • PMID:17825267
  • PMID:20214684
  • PMID:20921115
  • PMID:21049487
DOID:5419 schizophrenia MGI:87986 Mus musculus (house mouse) 11651 Akt1
  • MGI:6194238
  • PMID:14745448
DOID:2861 congenital nonspherocytic hemolytic anemia SGD:S000005185 Saccharomyces cerevisiae S288C 855480 ZWF1
  • MGI:6194238
  • PMID:14757426
DOID:10581 metachromatic leukodystrophy HGNC:713 Homo sapiens (human) 410 ARSA
  • MGI:6194238
  • PMID:15026521
  • PMID:15375602
  • RGD:7240710
DOID:0050770 polycystic liver disease HGNC:9411 Homo sapiens (human) 5589 PRKCSH
  • MGI:6194238
  • PMID:15057895
  • RGD:7240710
DOID:0050741 alcohol dependence RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a
  • MGI:6194238
  • PMID:15080502
  • PMID:8822536
DOID:0111100 maturity-onset diabetes of the young type 2 MGI:1270854 Mus musculus (house mouse) 103988 Gck
  • MGI:6194238
  • PMID:15102714
  • PMID:15161764
  • PMID:15569412
  • PMID:17353190
  • PMID:19952346
  • PMID:24447392
  • PMID:7553875
  • PMID:7665557
  • PMID:8530440
  • PMID:9867845
DOID:10763 hypertension HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:15106800
DOID:4483 rhinitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:15120189
DOID:9352 type 2 diabetes mellitus RGD:2670 Rattus norvegicus (Norway rat) 24385 Gck
  • MGI:6194238
  • PMID:15138155
  • PMID:22234649
DOID:9352 type 2 diabetes mellitus HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:15166380
  • PMID:18204829
  • PMID:18972094
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • MGI:6194238
  • PMID:15239085
  • PMID:18713296
  • PMID:22269154
  • PMID:26042596
  • PMID:27860427

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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: August 19, 2024