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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 70001 - 70025 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:1324 lung cancer HGNC:9801 Homo sapiens (human) 5879 RAC1
  • PMID:27299748
DOID:5419 schizophrenia HGNC:5234 Homo sapiens (human) 3305 HSPA1L
  • PMID:18299791
DOID:1612 breast cancer HGNC:7173 Homo sapiens (human) 4314 MMP3
  • PMID:17058024
DOID:10283 prostate cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • PMID:22815832
DOID:0060299 complement component 6 deficiency HGNC:1339 Homo sapiens (human) 729 C6
  • RGD:7240710
DOID:0050830 peripheral artery disease HGNC:18124 Homo sapiens (human) 64805 P2RY12
  • PMID:14662702
DOID:409 liver disease HGNC:4886 Homo sapiens (human) 3077 HFE
  • PMID:30651232
DOID:4186 articulation disorder HGNC:13830 Homo sapiens (human) 26047 CNTNAP2
  • PMID:25895914
DOID:9253 gastrointestinal stromal tumor HGNC:10681 Homo sapiens (human) 6390 SDHB
  • RGD:7240710
DOID:0111798 X-linked nephrolithiasis type I HGNC:2023 Homo sapiens (human) 1184 CLCN5
  • RGD:7240710
DOID:0080242 syndromic X-linked mental retardation Hough type HGNC:19701 Homo sapiens (human) 22866 CNKSR2
  • RGD:7240710
DOID:1612 breast cancer HGNC:17675 Homo sapiens (human) 57510 XPO5
  • PMID:21552306
DOID:4006 bladder urothelial carcinoma HGNC:12637 Homo sapiens (human) 7403 KDM6A
  • PMID:30352907
DOID:2917 cryoglobulinemia HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:28453396
DOID:0060875 isolated growth hormone deficiency type III HGNC:1133 Homo sapiens (human) 695 BTK
  • RGD:7240710
DOID:4448 macular degeneration HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:15829498
  • PMID:18172114
  • PMID:19628747
DOID:10534 stomach cancer HGNC:11726 Homo sapiens (human) 7011 TEP1
  • PMID:27305982
DOID:13078 eumycotic mycetoma HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:20184498
DOID:848 arthritis HGNC:3619 Homo sapiens (human) 2214 FCGR3A
  • PMID:19005160
  • PMID:19026120
DOID:10763 hypertension HGNC:2095 Homo sapiens (human) 1191 CLU
  • PMID:15925890
DOID:11830 myopia HGNC:7166 Homo sapiens (human) 4313 MMP2
  • PMID:20484597
DOID:10873 Kuhnt-Junius degeneration HGNC:7876 Homo sapiens (human) 4846 NOS3
  • PMID:23276910
DOID:9993 hypoglycemia HGNC:9291 Homo sapiens (human) 5506 PPP1R3A
  • PMID:9814479
DOID:0110975 brachydactyly type B2 HGNC:7866 Homo sapiens (human) 9241 NOG
  • PMID:17668388
  • PMID:22529972
  • RGD:7240710
DOID:0110285 autosomal recessive limb-girdle muscular dystrophy type 2Q HGNC:9069 Homo sapiens (human) 5339 PLEC
  • RGD:7240710

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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