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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 69051 - 69075 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:1287 cardiovascular system disease HGNC:333 Homo sapiens (human) 183 AGT
  • PMID:8523390
DOID:0080055 achondrogenesis type IB HGNC:10994 Homo sapiens (human) 1836 SLC26A2
  • PMID:8528239
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • PMID:8528240
DOID:10652 Alzheimer's disease HGNC:9060 Homo sapiens (human) 5333 PLCD1
  • PMID:8534418
DOID:10652 Alzheimer's disease HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:8534418
DOID:13316 exocrine pancreatic insufficiency HGNC:1884 Homo sapiens (human) 1080 CFTR
  • PMID:8535440
  • PMID:9254853
DOID:2256 osteochondrodysplasia MGI:109349 Mus musculus (house mouse) 11909 Atf2
  • PMID:8538792
DOID:10763 hypertension RGD:3783 Rattus norvegicus (Norway rat) 24800 Sts
  • PMID:8539776
DOID:1520 colon carcinoma HGNC:12458 Homo sapiens (human) 7311 UBA52
  • PMID:8541345
DOID:1909 melanoma HGNC:11180 Homo sapiens (human) 6648 SOD2
  • PMID:8541726
DOID:552 pneumonia HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • PMID:8542113
DOID:0060074 ductal carcinoma in situ HGNC:651 Homo sapiens (human) 374 AREG
  • PMID:8543395
DOID:635 acquired immunodeficiency syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:8548330
DOID:635 acquired immunodeficiency syndrome HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:8548330
DOID:635 acquired immunodeficiency syndrome HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A
  • PMID:8548330
DOID:12236 primary biliary cholangitis HGNC:6518 Homo sapiens (human) 3930 LBR
  • PMID:8550049
DOID:2224 essential thrombocythemia HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:8555064
DOID:8997 polycythemia vera HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:8555064
DOID:8552 chronic myeloid leukemia HGNC:1663 Homo sapiens (human) 948 CD36
  • PMID:8555064
DOID:10964 cholesteatoma of middle ear HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:8562031
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:3765 Homo sapiens (human) 2322 FLT3
  • PMID:8562934
DOID:9952 acute lymphoblastic leukemia HGNC:2466 Homo sapiens (human) 1464 CSPG4
  • PMID:8562939
DOID:3393 coronary artery disease HGNC:3662 Homo sapiens (human) 2244 FGB
  • PMID:8565160
DOID:12930 dilated cardiomyopathy HGNC:6180 Homo sapiens (human) 3708 ITPR1
  • PMID:8567977
DOID:11372 megacolon RGD:2536 Rattus norvegicus (Norway rat) 50672 Ednrb
  • PMID:8570650

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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