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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 68826 - 68850 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0060309 syndromic X-linked intellectual disability HGNC:29873 Homo sapiens (human) 79576 NKAP
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:11021356
DOID:12306 vitiligo HGNC:1323 Homo sapiens (human) 720 C4A
  • PMID:21943165
DOID:14757 Ehlers-Danlos syndrome hypermobility type HGNC:2201 Homo sapiens (human) 1281 COL3A1
  • PMID:7833919
DOID:9256 colorectal cancer HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:30489355
DOID:1067 open-angle glaucoma HGNC:43 Homo sapiens (human) 6890 TAP1
  • PMID:15887980
DOID:3905 lung carcinoma RGD:70487 Rattus norvegicus (Norway rat) 84353 Ctnnb1
  • PMID:17639448
DOID:9352 type 2 diabetes mellitus HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:18771471
DOID:0050565 autosomal recessive nonsyndromic deafness HGNC:33914 Homo sapiens (human) 100127206 MINAR2
  • RGD:7240710
DOID:10211 cholelithiasis HGNC:12530 Homo sapiens (human) 54658 UGT1A1
  • PMID:10498597
  • PMID:17593033
  • PMID:18081723
DOID:0110196 Charcot-Marie-Tooth disease type 4G HGNC:4922 Homo sapiens (human) 3098 HK1
  • RGD:7240710
DOID:670 amphetamine abuse HGNC:4087 Homo sapiens (human) 2566 GABRG2
  • PMID:14569258
DOID:0090056 dystonia 12 HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:19087156
DOID:9744 type 1 diabetes mellitus HGNC:11588 Homo sapiens (human) 6908 TBP
  • PMID:15381080
  • PMID:15850778
DOID:9974 drug dependence HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:24455721
DOID:13375 temporal arteritis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:16846526
  • PMID:20064872
DOID:13001 carotid stenosis HGNC:7406 Homo sapiens (human) 4502 MT2A
  • PMID:17622311
DOID:2986 IgA glomerulonephritis HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:12220450
DOID:0060645 chronic recurrent multifocal osteomyelitis HGNC:14450 Homo sapiens (human) 9663 LPIN2
  • RGD:7240710
DOID:0112008 pituitary adenoma 5 HGNC:13733 Homo sapiens (human) 64072 CDH23
  • RGD:7240710
DOID:10873 Kuhnt-Junius degeneration HGNC:12680 Homo sapiens (human) 7422 VEGFA
  • PMID:23149126
  • PMID:23745581
DOID:0060708 lymphoproliferative syndrome 2 HGNC:11922 Homo sapiens (human) 939 CD27
  • RGD:7240710
DOID:0080822 aspirin-induced respiratory disease HGNC:11608 Homo sapiens (human) 6915 TBXA2R
  • PMID:15898979
DOID:0112313 brain small vessel disease HGNC:3661 Homo sapiens (human) 2243 FGA
  • PMID:17951283
DOID:0111183 familial hemiplegic migraine 3 HGNC:10585 Homo sapiens (human) 6323 SCN1A
  • 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