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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 July 29, 2024
Displaying entries 3401 - 3425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence Code Names References
DOID:0060001 withdrawal disorder HGNC:4092 Homo sapiens (human) 2571 GAD1
  • MGI:6194238
  • PMID:19111404
DOID:12894 Sjogren's syndrome HGNC:1119 Homo sapiens (human) 684 BST2
  • PMID:30249485
DOID:0110297 autosomal recessive limb-girdle muscular dystrophy type 2K Xenbase:XB-GENE-6488680 Xenopus laevis (African clawed frog) 108699937 pomt1.S
  • MGI:6194238
DOID:7148 rheumatoid arthritis HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:12739037
DOID:0050696 fetal alcohol spectrum disorder HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
DOID:3770 pulmonary fibrosis FB:FBgn0064237 Drosophila melanogaster (fruit fly) 37104 Idgf5
  • MGI:6194238
DOID:12716 newborn respiratory distress syndrome HGNC:10799 Homo sapiens (human) 729238 SFTPA2
  • MGI:6194238
  • PMID:9475280
DOID:2747 glycogen storage disease ZFIN:ZDB-GENE-030826-31 Danio rerio (zebrafish) 373082 gys2
  • MGI:6194238
DOID:0080101 Compton-North congenital myopathy HGNC:2171 Homo sapiens (human) 1272 CNTN1
  • MGI:6194238
  • RGD:7240710
DOID:3083 chronic obstructive pulmonary disease MGI:104993 Mus musculus (house mouse) 16847 Lepr
  • MGI:6194238
DOID:12217 Lewy body dementia HGNC:8729 Homo sapiens (human) 5111 PCNA
  • PMID:20665591
DOID:0111042 glycogen storage disease IXa HGNC:8926 Homo sapiens (human) 5256 PHKA2
  • MGI:6194238
  • PMID:28283841
  • PMID:28627441
  • PMID:8733134
  • RGD:7240710
DOID:0081139 agammaglobulinemia 7 RGD:3329 Rattus norvegicus (Norway rat) 25513 Pik3r1
  • MGI:6194238
DOID:0112343 hereditary spastic paraplegia 82 HGNC:8756 Homo sapiens (human) 5833 PCYT2
  • RGD:7240710
DOID:0050127 sinusitis FB:FBgn0262473 Drosophila melanogaster (fruit fly) 43222 Tl
  • MGI:6194238
DOID:1380 endometrial cancer HGNC:8905 Homo sapiens (human) 5236 PGM1
  • PMID:508567
DOID:557 kidney disease HGNC:6530 Homo sapiens (human) 3938 LCT
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 SGD:S000000208 Saccharomyces cerevisiae S288C 852289 GPI18
  • MGI:6194238
DOID:12801 mucopolysaccharidosis III HGNC:4422 Homo sapiens (human) 2799 GNS
  • MGI:6194238
  • PMID:12573255
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q FB:FBgn0039827 Drosophila melanogaster (fruit fly) 43689 CG1544
  • MGI:6194238
DOID:11151 cholecystolithiasis FB:FBgn0040260 Drosophila melanogaster (fruit fly) 53511 Ugt37D1
  • MGI:6194238
DOID:0080470 developmental and epileptic encephalopathy 36 ZFIN:ZDB-GENE-060307-1 Danio rerio (zebrafish) 557181 alg13
  • MGI:6194238
DOID:10247 pleurisy HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
DOID:1580 diffuse scleroderma HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:21905008
DOID:12361 Graves' disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15219383
  • PMID:17348243
  • PMID:19732761

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Supported by JST NBDC Grant Number JPMJND2204

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