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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 70401 - 70425 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
  • PMID:19034968
  • PMID:25219124
DOID:0110423 dilated cardiomyopathy 1C MGI:1344412 Mus musculus (house mouse) 24131 Ldb3
  • MGI:6194238
  • PMID:19028670
DOID:9775 diastolic heart failure HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:19021695
  • PMID:19752885
DOID:2841 asthma HGNC:1604 Homo sapiens (human) 1232 CCR3
  • MGI:6194238
  • PMID:19017998
  • PMID:20220260
DOID:5733 salpingitis RGD:2332 Rattus norvegicus (Norway rat) 24255 Cftr
  • MGI:6194238
  • PMID:19012687
DOID:5733 salpingitis HGNC:1884 Homo sapiens (human) 1080 CFTR
  • MGI:6194238
  • PMID:19012687
DOID:10763 hypertension HGNC:277 Homo sapiens (human) 148 ADRA1A
  • MGI:6194238
  • PMID:19011682
DOID:11726 Emery-Dreifuss muscular dystrophy MGI:1927152 Mus musculus (house mouse) 64009 Syne1
  • MGI:6194238
  • PMID:19008300
DOID:14694 Johanson-Blizzard syndrome HGNC:16808 Homo sapiens (human) 197131 UBR1
  • MGI:6194238
  • PMID:19006206
  • PMID:21711208
  • RGD:7240710
DOID:9975 cocaine dependence HGNC:2345 Homo sapiens (human) 1385 CREB1
  • MGI:6194238
  • PMID:19001277
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:6430 Homo sapiens (human) 3875 KRT18
  • MGI:6194238
  • PMID:18995215
  • PMID:19333204
  • PMID:19585618
  • PMID:21993925
  • PMID:24630506
DOID:0080052 acromesomelic dysplasia, Grebe type HGNC:4220 Homo sapiens (human) 8200 GDF5
  • MGI:6194238
  • PMID:18979166
  • PMID:19038017
  • PMID:23812741
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6091 Homo sapiens (human) 3643 INSR
  • MGI:6194238
  • PMID:18972094
DOID:6432 pulmonary hypertension HGNC:7876 Homo sapiens (human) 4846 NOS3
  • MGI:6194238
  • PMID:18953956
  • PMID:19912632
  • PMID:21111729
  • PMID:21144100
  • PMID:25699607
DOID:332 amyotrophic lateral sclerosis HGNC:11179 Homo sapiens (human) 6647 SOD1
  • MGI:6194238
  • PMID:18947433
  • PMID:23147550
  • PMID:26826269
DOID:9970 obesity RGD:2432 Rattus norvegicus (Norway rat) 25307 Cst3
  • MGI:6194238
  • PMID:18946178
DOID:0110248 cataract 30 MGI:98932 Mus musculus (house mouse) 22352 Vim
  • MGI:6194238
  • PMID:18940912
DOID:9351 diabetes mellitus HGNC:6091 Homo sapiens (human) 3643 INSR
  • MGI:6194238
  • PMID:18925540
DOID:3393 coronary artery disease HGNC:3176 Homo sapiens (human) 1906 EDN1
  • MGI:6194238
  • PMID:18923236
  • PMID:7968078
DOID:13533 osteopetrosis MGI:1339753 Mus musculus (house mouse) 12977 Csf1
  • MGI:6194238
  • PMID:1887865
DOID:1936 atherosclerosis HGNC:1514 Homo sapiens (human) 846 CASR
  • MGI:6194238
  • PMID:18852253
DOID:0110471 autosomal recessive nonsyndromic deafness 16 MGI:2153816 Mus musculus (house mouse) 140476 Strc
  • MGI:6194238
  • PMID:18849963
DOID:8947 diabetic retinopathy RGD:3186 Rattus norvegicus (Norway rat) 24600 Nos3
  • MGI:6194238
  • PMID:18840783
  • PMID:23059402
DOID:684 hepatocellular carcinoma HGNC:1748 Homo sapiens (human) 999 CDH1
  • MGI:6194238
  • PMID:18837082
  • PMID:30697077
DOID:8947 diabetic retinopathy HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
  • PMID:18834676
  • PMID:18942221

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Last updated: December 9, 2024