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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 68251 - 68275 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:1883 hepatitis C HGNC:6338 Homo sapiens (human) 3811 KIR3DL1
  • PMID:28225833
DOID:409 liver disease HGNC:2321 Homo sapiens (human) 1371 CPOX
  • PMID:7849704
DOID:10247 pleurisy HGNC:8583 Homo sapiens (human) 5054 SERPINE1
  • PMID:23052617
DOID:2394 ovarian cancer HGNC:952 Homo sapiens (human) 580 BARD1
  • PMID:16152612
DOID:0110131 Bardet-Biedl syndrome 9 HGNC:30000 Homo sapiens (human) 27241 BBS9
  • RGD:7240710
DOID:0070234 Loeys-Dietz syndrome 2 HGNC:11773 Homo sapiens (human) 7048 TGFBR2
  • RGD:7240710
DOID:0060807 syndromic X-linked intellectual disability Najm type HGNC:1497 Homo sapiens (human) 8573 CASK
  • RGD:7240710
DOID:0110440 dilated cardiomyopathy 1J HGNC:3522 Homo sapiens (human) 2070 EYA4
  • RGD:7240710
DOID:0110681 congenital myasthenic syndrome 2A HGNC:1961 Homo sapiens (human) 1140 CHRNB1
  • RGD:7240710
DOID:0050745 diffuse large B-cell lymphoma HGNC:7562 Homo sapiens (human) 4615 MYD88
  • PMID:25347427
  • PMID:28803429
  • PMID:31609782
DOID:0110820 hereditary spastic paraplegia 75 HGNC:6783 Homo sapiens (human) 4099 MAG
  • RGD:7240710
DOID:0110098 atopic dermatitis 2 HGNC:3748 Homo sapiens (human) 2312 FLG
  • RGD:7240710
DOID:5327 retinal detachment HGNC:2200 Homo sapiens (human) 1280 COL2A1
  • PMID:22574936
DOID:0090102 autosomal dominant macrothrombocytopenia TUBB1-related HGNC:16257 Homo sapiens (human) 81027 TUBB1
  • RGD:7240710
DOID:2841 asthma HGNC:4932 Homo sapiens (human) 3106 HLA-B
  • PMID:28380482
DOID:10534 stomach cancer HGNC:3438 Homo sapiens (human) 2074 ERCC6
  • PMID:27340861
DOID:0070139 autosomal recessive cutis laxa type IC HGNC:6717 Homo sapiens (human) 8425 LTBP4
  • RGD:7240710
DOID:2452 thrombophilia HGNC:3661 Homo sapiens (human) 2243 FGA
  • PMID:10910940
DOID:0111130 focal segmental glomerulosclerosis 5 HGNC:23791 Homo sapiens (human) 64423 INF2
  • RGD:7240710
DOID:10283 prostate cancer HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:26788504
DOID:0080301 atypical hemolytic-uremic syndrome HGNC:4888 Homo sapiens (human) 3078 CFHR1
  • PMID:23243267
  • RGD:7240710
DOID:0050589 inflammatory bowel disease HGNC:25240 Homo sapiens (human) 196527 ANO6
  • PMID:23308121
DOID:0060901 lymphoplasmacytic lymphoma HGNC:5962 Homo sapiens (human) 3586 IL10
  • PMID:19573080
DOID:9970 obesity HGNC:29849 Homo sapiens (human) 253559 CADM2
  • PMID:31341224
DOID:8398 osteoarthritis HGNC:190 Homo sapiens (human) 8038 ADAM12
  • PMID:15334463

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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