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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 66876 - 66900 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:3008 invasive ductal carcinoma HGNC:16806 Homo sapiens (human) 51366 UBR5
  • PMID:14871824
DOID:10584 retinitis pigmentosa HGNC:29253 Homo sapiens (human) 57545 CC2D2A
  • RGD:7240710
DOID:1612 breast cancer HGNC:2095 Homo sapiens (human) 1191 CLU
  • PMID:22037783
DOID:0070482 spinal neurofibromatosis HGNC:7765 Homo sapiens (human) 4763 NF1
  • RGD:7240710
DOID:3324 mood disorder HGNC:240 Homo sapiens (human) 115 ADCY9
  • PMID:11840511
DOID:1596 depressive disorder HGNC:4079 Homo sapiens (human) 2558 GABRA5
  • PMID:9267853
DOID:676 juvenile rheumatoid arthritis HGNC:5991 Homo sapiens (human) 3552 IL1A
  • PMID:8162643
DOID:0070405 hypomyelinating leukodystrophy 16 HGNC:22407 Homo sapiens (human) 54664 TMEM106B
  • RGD:7240710
DOID:6039 uveal melanoma HGNC:6919 Homo sapiens (human) 8930 MBD4
  • RGD:7240710
DOID:8924 autoimmune thrombocytopenic purpura HGNC:3619 Homo sapiens (human) 2214 FCGR3A
  • PMID:11380443
  • PMID:22123287
  • PMID:23484707
DOID:11984 hypertrophic cardiomyopathy HGNC:7551 Homo sapiens (human) 4607 MYBPC3
  • PMID:15519027
  • PMID:15737656
DOID:9351 diabetes mellitus HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:16303885
  • PMID:16788382
DOID:0112238 X-linked lissencephaly 2 HGNC:18060 Homo sapiens (human) 170302 ARX
  • PMID:12379852
  • RGD:7240710
DOID:2583 agammaglobulinemia HGNC:19027 Homo sapiens (human) 56262 LRRC8A
  • PMID:14660746
DOID:8791 breast carcinoma in situ HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:8649861
DOID:3083 chronic obstructive pulmonary disease HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • PMID:28900078
DOID:0112026 non-syndromic X-linked intellectual disability 99 HGNC:12632 Homo sapiens (human) 8239 USP9X
  • RGD:7240710
DOID:0111916 spermatogenic failure 28 HGNC:23168 Homo sapiens (human) 57697 FANCM
  • RGD:7240710
DOID:0080663 atrial standstill 2 HGNC:7939 Homo sapiens (human) 4878 NPPA
  • RGD:7240710
DOID:1070 primary open angle glaucoma HGNC:9204 Homo sapiens (human) 5444 PON1
  • PMID:22553514
DOID:0111854 primary ciliary dyskinesia 39 HGNC:25430 Homo sapiens (human) 115399 LRRC56
  • RGD:7240710
DOID:0070296 primary autosomal recessive microcephaly HGNC:24054 Homo sapiens (human) 57082 KNL1
  • PMID:22983954
DOID:1070 primary open angle glaucoma HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:22831837
DOID:2986 IgA glomerulonephritis HGNC:244 Homo sapiens (human) 119 ADD2
  • PMID:19838659
DOID:5426 primary ovarian insufficiency HGNC:26520 Homo sapiens (human) 147872 KASH5
  • RGD:7240710

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International Collaboration

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