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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 70826 - 70850 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:10763 hypertension HGNC:259 Homo sapiens (human) 133 ADM
  • MGI:6194238
  • PMID:16625237
DOID:0080652 calcium oxalate nephrolithiasis HGNC:453 Homo sapiens (human) 259 AMBP
  • MGI:6194238
  • PMID:16622176
DOID:9352 type 2 diabetes mellitus HGNC:8724 Homo sapiens (human) 5105 PCK1
  • MGI:6194238
  • PMID:16620271
  • PMID:16978381
  • PMID:19070910
DOID:4989 pancreatitis HGNC:10632 Homo sapiens (human) 6352 CCL5
  • MGI:6194238
  • PMID:16614115
DOID:0090003 agenesis of the corpus callosum with peripheral neuropathy HGNC:10914 Homo sapiens (human) 9990 SLC12A6
  • MGI:6194238
  • PMID:16606917
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:428 Homo sapiens (human) 7840 ALMS1
  • MGI:6194238
  • PMID:16601972
DOID:0090125 brain small vessel disease 1 MGI:88454 Mus musculus (house mouse) 12826 Col4a1
  • MGI:6194238
  • PMID:16598045
DOID:9744 type 1 diabetes mellitus MGI:107474 Mus musculus (house mouse) 12494 Cd38
  • MGI:6194238
  • PMID:16585549
DOID:14330 Parkinson's disease HGNC:5244 Homo sapiens (human) 3313 HSPA9
  • MGI:6194238
  • PMID:16565515
  • PMID:18219256
  • PMID:19657588
  • PMID:20817635
DOID:9970 obesity RGD:2797 Rattus norvegicus (Norway rat) 25059 Hk2
  • MGI:6194238
  • PMID:16555472
DOID:5419 schizophrenia HGNC:4586 Homo sapiens (human) 2904 GRIN2B
  • MGI:6194238
  • PMID:16549338
  • PMID:17224684
DOID:5844 myocardial infarction HGNC:11766 Homo sapiens (human) 7040 TGFB1
  • MGI:6194238
  • PMID:16543493
DOID:1561 cognitive disorder HGNC:2228 Homo sapiens (human) 1312 COMT
  • MGI:6194238
  • PMID:16542182
  • PMID:31301644
DOID:3672 rhabdoid cancer HGNC:11103 Homo sapiens (human) 6598 SMARCB1
  • MGI:6194238
  • PMID:16528370
  • PMID:9671307
DOID:4603 epidermolytic hyperkeratosis MGI:96698 Mus musculus (house mouse) 16678 Krt1
  • MGI:6194238
  • PMID:16528356
DOID:10763 hypertension HGNC:336 Homo sapiens (human) 185 AGTR1
  • MGI:6194238
  • PMID:16519598
  • PMID:9456365
DOID:11247 disseminated intravascular coagulation HGNC:6018 Homo sapiens (human) 3569 IL6
  • MGI:6194238
  • PMID:16518755
  • PMID:16613997
DOID:3526 cerebral infarction RGD:2865 Rattus norvegicus (Norway rat) 24481 Ifnb1
  • MGI:6194238
  • PMID:16514094
DOID:0111441 optic atrophy 1 HGNC:8140 Homo sapiens (human) 4976 OPA1
  • MGI:6194238
  • PMID:16513463
  • PMID:16617242
  • PMID:17306754
  • PMID:19112530
  • PMID:20546606
  • PMID:23401657
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
  • PMID:16505242
DOID:10763 hypertension HGNC:244 Homo sapiens (human) 119 ADD2
  • MGI:6194238
  • PMID:16497648
  • PMID:24652215
DOID:6000 congestive heart failure RGD:2956 Rattus norvegicus (Norway rat) 25471 Kcne1
  • MGI:6194238
  • PMID:16497176
DOID:0050540 Charcot-Marie-Tooth disease type 3 MGI:103177 Mus musculus (house mouse) 17528 Mpz
  • MGI:6194238
  • PMID:16495463
  • PMID:7581451
DOID:3393 coronary artery disease HGNC:11935 Homo sapiens (human) 959 CD40LG
  • MGI:6194238
  • PMID:16494885
  • PMID:17635572
  • PMID:22645426
DOID:9970 obesity HGNC:6018 Homo sapiens (human) 3569 IL6
  • MGI:6194238
  • PMID:16493118
  • PMID:19228869

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Last updated: December 9, 2024