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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 64726 - 64750 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:1909 melanoma HGNC:6929 Homo sapiens (human) 4157 MC1R
  • PMID:17434924
  • PMID:8894704
DOID:6000 congestive heart failure HGNC:3522 Homo sapiens (human) 2070 EYA4
  • PMID:15735644
DOID:2377 multiple sclerosis HGNC:7067 Homo sapiens (human) 4261 CIITA
  • PMID:15821736
  • PMID:16426246
  • PMID:21653641
DOID:0060821 syndromic X-linked intellectual disability 14 HGNC:20439 Homo sapiens (human) 65109 UPF3B
  • RGD:7240710
DOID:0050589 inflammatory bowel disease HGNC:5472 Homo sapiens (human) 3486 IGFBP3
  • PMID:15844718
DOID:9352 type 2 diabetes mellitus HGNC:4242 Homo sapiens (human) 9945 GFPT2
  • PMID:14764791
DOID:1588 thrombocytopenia HGNC:7579 Homo sapiens (human) 4627 MYH9
  • PMID:10973259
DOID:3369 Ewing sarcoma HGNC:3508 Homo sapiens (human) 2130 EWSR1
  • PMID:1522903
  • RGD:7240710
DOID:0081015 congenital fibrosis of the extraocular muscles 1 HGNC:19349 Homo sapiens (human) 55605 KIF21A
  • PMID:14595441
  • RGD:7240710
DOID:0060060 non-Hodgkin lymphoma HGNC:20185 Homo sapiens (human) 54916 TMEM260
  • PMID:24831772
DOID:2987 familial mediterranean fever HGNC:8583 Homo sapiens (human) 5054 SERPINE1
  • PMID:22736074
DOID:1883 hepatitis C HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:21535077
DOID:0080589 Klippel-Feil syndrome 1 HGNC:4221 Homo sapiens (human) 392255 GDF6
  • RGD:7240710
DOID:3146 lipid metabolism disorder HGNC:2859 Homo sapiens (human) 1718 DHCR24
  • PMID:11519011
DOID:4186 articulation disorder HGNC:13875 Homo sapiens (human) 93986 FOXP2
  • PMID:20923434
DOID:2747 glycogen storage disease HGNC:4699 Homo sapiens (human) 2992 GYG1
  • RGD:7240710
DOID:0050697 chorioamnionitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15128916
DOID:9256 colorectal cancer HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • PMID:29804528
DOID:9352 type 2 diabetes mellitus HGNC:6636 Homo sapiens (human) 4000 LMNA
  • PMID:17327437
  • PMID:17327461
DOID:12399 pathological gambling HGNC:3025 Homo sapiens (human) 1815 DRD4
  • PMID:10402503
DOID:12960 acrocephalosyndactylia HGNC:12428 Homo sapiens (human) 7291 TWIST1
  • PMID:8988166
DOID:0080924 bilateral perisylvian polymicrogyria HGNC:4512 Homo sapiens (human) 9289 ADGRG1
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:17675 Homo sapiens (human) 57510 XPO5
  • PMID:24676133
DOID:2859 hemoglobin C disease HGNC:4827 Homo sapiens (human) 3043 HBB
  • PMID:2239966

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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