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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 69801 - 69825 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:10873 Kuhnt-Junius degeneration HGNC:5394 Homo sapiens (human) 3426 CFI
  • PMID:23900096
DOID:1205 allergic disease HGNC:17451 Homo sapiens (human) 10800 CYSLTR1
  • PMID:16776674
DOID:2841 asthma HGNC:16711 Homo sapiens (human) 10333 TLR6
  • PMID:15266299
  • PMID:18547625
DOID:0050776 non-syndromic X-linked intellectual disability HGNC:2484 Homo sapiens (human) 1478 CSTF2
  • RGD:7240710
DOID:13139 crescentic glomerulonephritis RGD:71069 Rattus norvegicus (Norway rat) 116591 Fcgr2a
  • PMID:16482158
DOID:0111260 phosphoribosylpyrophosphate synthetase superactivity HGNC:9462 Homo sapiens (human) 5631 PRPS1
  • RGD:7240710
DOID:7693 abdominal aortic aneurysm HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:16879749
DOID:0080205 CAKUT HGNC:1071 Homo sapiens (human) 652 BMP4
  • PMID:24131739
DOID:0070033 autosomal dominant intellectual developmental disorder 3 HGNC:1754 Homo sapiens (human) 1013 CDH15
  • RGD:7240710
DOID:8029 sporadic breast cancer HGNC:8912 Homo sapiens (human) 5245 PHB1
  • PMID:1540973
DOID:2747 glycogen storage disease HGNC:9725 Homo sapiens (human) 5836 PYGL
  • PMID:9536091
DOID:526 human immunodeficiency virus infectious disease HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • PMID:18096355
DOID:0081337 congenital myopathy HGNC:9639 Homo sapiens (human) 9200 HACD1
  • RGD:7240710
DOID:0050671 female breast cancer HGNC:26144 Homo sapiens (human) 79728 PALB2
  • PMID:30303537
DOID:9256 colorectal cancer HGNC:14897 Homo sapiens (human) 80271 ITPKC
  • PMID:33470690
DOID:705 Leber hereditary optic neuropathy HGNC:7461 Homo sapiens (human) 4540 MT-ND5
  • PMID:16240359
  • PMID:16816025
  • PMID:1732158
  • PMID:19022198
  • PMID:21131053
DOID:4988 alcoholic pancreatitis HGNC:12539 Homo sapiens (human) 54577 UGT1A7
  • PMID:12806614
DOID:4483 rhinitis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:16950285
  • PMID:20109306
DOID:2513 basal cell carcinoma HGNC:13723 Homo sapiens (human) 10664 CTCF
  • PMID:27974201
DOID:0080232 autosomal dominant intellectual developmental disorder 51 HGNC:24283 Homo sapiens (human) 51111 KMT5B
  • RGD:7240710
DOID:8947 diabetic retinopathy HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1
  • PMID:23837223
DOID:0080076 Neu-Laxova syndrome 1 HGNC:8923 Homo sapiens (human) 26227 PHGDH
  • RGD:7240710
DOID:3482 plague RGD:620596 Rattus norvegicus (Norway rat) 117029 Ccr5
  • PMID:18703167
DOID:9952 acute lymphoblastic leukemia HGNC:1014 Homo sapiens (human) 613 BCR
  • RGD:7240710
DOID:0070182 spermatogenic failure 13 HGNC:11538 Homo sapiens (human) 6875 TAF4B
  • 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