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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 70876 - 70900 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:9452 steatotic liver disease RGD:3369 Rattus norvegicus (Norway rat) 25747 Ppara
  • MGI:6194238
  • PMID:16393287
DOID:9452 steatotic liver disease HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
  • PMID:16393287
DOID:783 end stage renal disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:16385653
  • PMID:20149750
DOID:0090031 D-bifunctional protein deficiency HGNC:5213 Homo sapiens (human) 3295 HSD17B4
  • MGI:6194238
  • PMID:16385454
  • PMID:9345094
  • RGD:7240710
DOID:1935 Bardet-Biedl syndrome HGNC:30000 Homo sapiens (human) 27241 BBS9
  • MGI:6194238
  • PMID:16380913
DOID:0060747 Duane-radial ray syndrome MGI:2139360 Mus musculus (house mouse) 99377 Sall4
  • MGI:6194238
  • PMID:16380715
  • PMID:16790473
  • PMID:17216607
DOID:3633 beta-mannosidosis MGI:88175 Mus musculus (house mouse) 110173 Manba
  • MGI:6194238
  • PMID:16377659
DOID:10763 hypertension RGD:2055 Rattus norvegicus (Norway rat) 29412 Adra1a
  • MGI:6194238
  • PMID:16371063
DOID:10652 Alzheimer's disease HGNC:11180 Homo sapiens (human) 6648 SOD2
  • MGI:6194238
  • PMID:16369462
DOID:552 pneumonia HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • MGI:6194238
  • PMID:16369129
  • PMID:18838927
  • PMID:19900796
DOID:2843 long QT syndrome RGD:621503 Rattus norvegicus (Norway rat) 84020 Kcnq1
  • MGI:6194238
  • PMID:16368876
DOID:0050947 hereditary hypophosphatemic rickets with hypercalciuria HGNC:11019 Homo sapiens (human) 6569 SLC34A1
  • MGI:6194238
  • PMID:16358215
DOID:10763 hypertension RGD:3717 Rattus norvegicus (Norway rat) 29715 Slc8a1
  • MGI:6194238
  • PMID:16343576
DOID:6432 pulmonary hypertension HGNC:11050 Homo sapiens (human) 6532 SLC6A4
  • MGI:6194238
  • PMID:16339917
  • PMID:16399993
  • PMID:19556740
  • PMID:19736308
  • PMID:19886858
DOID:14330 Parkinson's disease HGNC:10935 Homo sapiens (human) 6571 SLC18A2
  • MGI:6194238
  • PMID:16339215
  • PMID:16421508
DOID:0050570 congenital disorder of glycosylation type I MGI:97075 Mus musculus (house mouse) 110119 Mpi
  • MGI:6194238
  • PMID:16339137
DOID:0110670 congenital myasthenic syndrome 9 MGI:103581 Mus musculus (house mouse) 18198 Musk
  • MGI:6194238
  • PMID:16337809
  • PMID:18718936
DOID:684 hepatocellular carcinoma HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • MGI:6194238
  • PMID:16331247
  • PMID:24673525
  • PMID:26823876
  • RGD:7240710
DOID:5688 Werner syndrome MGI:109635 Mus musculus (house mouse) 22427 Wrn
  • MGI:6194238
  • PMID:16330174
DOID:10283 prostate cancer HGNC:583 Homo sapiens (human) 324 APC
  • MGI:6194238
  • PMID:16322291
DOID:2349 arteriosclerosis RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9
  • MGI:6194238
  • PMID:16317521
DOID:1936 atherosclerosis RGD:708418 Rattus norvegicus (Norway rat) 84349 Cd40lg
  • MGI:6194238
  • PMID:16317521
  • PMID:23984971
  • PMID:26261622
DOID:0060316 orofaciodigital syndrome I MGI:1350328 Mus musculus (house mouse) 237222 Ofd1
  • MGI:6194238
  • PMID:16311594
DOID:3012 Li-Fraumeni syndrome HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:1631137
DOID:2316 brain ischemia HGNC:5981 Homo sapiens (human) 3605 IL17A
  • MGI:6194238
  • PMID:16305645

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Last updated: December 9, 2024