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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 70076 - 70100 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:9976 heroin dependence RGD:620218 Rattus norvegicus (Norway rat) 81646 Creb1
  • MGI:6194238
  • PMID:21362452
  • PMID:23062870
DOID:0060869 late-onset retinal degeneration MGI:2385958 Mus musculus (house mouse) 235312 C1qtnf5
  • MGI:6194238
  • PMID:21349921
  • PMID:22110650
DOID:0111253 neurofibromatosis 1 HGNC:7765 Homo sapiens (human) 4763 NF1
  • MGI:6194238
  • PMID:2134734
  • PMID:32575496
  • RGD:7240710
DOID:12466 secondary hyperparathyroidism RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2
  • MGI:6194238
  • PMID:21335517
DOID:12466 secondary hyperparathyroidism HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:21335517
DOID:5844 myocardial infarction RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
  • PMID:21329947
DOID:83 cataract HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:21329682
  • PMID:24360973
DOID:1612 breast cancer MGI:1206581 Mus musculus (house mouse) 18706 Pik3ca
  • MGI:6194238
  • PMID:21324922
  • PMID:22370636
  • PMID:22666336
DOID:2841 asthma HGNC:14900 Homo sapiens (human) 50616 IL22
  • MGI:6194238
  • PMID:21297073
  • PMID:21535180
DOID:9352 type 2 diabetes mellitus HGNC:24678 Homo sapiens (human) 79068 FTO
  • MGI:6194238
  • PMID:21294771
  • PMID:25303482
  • PMID:28890888
  • PMID:29154870
  • PMID:29410390
  • PMID:32061761
DOID:1852 intrahepatic cholestasis MGI:97569 Mus musculus (house mouse) 18670 Abcb4
  • MGI:6194238
  • PMID:21292027
DOID:11612 polycystic ovary syndrome HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
  • PMID:21282199
DOID:7693 abdominal aortic aneurysm RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9
  • MGI:6194238
  • PMID:21256058
DOID:0050800 cerebral creatine deficiency syndrome 1 MGI:2147834 Mus musculus (house mouse) 102857 Slc6a8
  • MGI:6194238
  • PMID:21249153
  • PMID:22751104
  • PMID:25485098
  • PMID:27466184
  • PMID:30013483
DOID:0110083 arrhythmogenic right ventricular dysplasia 12 MGI:96650 Mus musculus (house mouse) 16480 Jup
  • MGI:6194238
  • PMID:21245375
  • PMID:21880664
  • PMID:22021931
DOID:5844 myocardial infarction RGD:61914 Rattus norvegicus (Norway rat) 29436 Tfpi
  • MGI:6194238
  • PMID:21229253
DOID:14219 renal tubular acidosis MGI:1927555 Mus musculus (house mouse) 54403 Slc4a4
  • MGI:6194238
  • PMID:21228764
DOID:3969 thyroid gland papillary carcinoma MGI:88190 Mus musculus (house mouse) 109880 Braf
  • MGI:6194238
  • PMID:21220306
  • PMID:21512141
DOID:9970 obesity HGNC:3535 Homo sapiens (human) 2147 F2
  • MGI:6194238
  • PMID:21210148
DOID:14789 spondyloepiphyseal dysplasia congenita HGNC:2200 Homo sapiens (human) 1280 COL2A1
  • MGI:6194238
  • PMID:21204228
  • PMID:23079993
  • RGD:7240710
DOID:12930 dilated cardiomyopathy MGI:98352 Mus musculus (house mouse) 20656 Sod2
  • MGI:6194238
  • PMID:21195081
DOID:0060861 microphthalmia with limb anomalies MGI:1929878 Mus musculus (house mouse) 64075 Smoc1
  • MGI:6194238
  • PMID:21194678
  • PMID:21750680
DOID:5844 myocardial infarction RGD:2069 Rattus norvegicus (Norway rat) 24179 Agt
  • MGI:6194238
  • PMID:21167013
DOID:10652 Alzheimer's disease MGI:96828 Mus musculus (house mouse) 16971 Lrp1
  • MGI:6194238
  • PMID:21159977
DOID:850 lung disease HGNC:2438 Homo sapiens (human) 1440 CSF3
  • MGI:6194238
  • PMID:21155037

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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