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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 70876 - 70900 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050560 Walker-Warburg syndrome HGNC:13530 Homo sapiens (human) 10329 RXYLT1
  • MGI:6194238
DOID:3910 lung adenocarcinoma HGNC:380 Homo sapiens (human) 10327 AKR1A1
  • PMID:30727821
DOID:1612 breast cancer HGNC:380 Homo sapiens (human) 10327 AKR1A1
  • PMID:25526449
DOID:3910 lung adenocarcinoma HGNC:13176 Homo sapiens (human) 10320 IKZF1
  • PMID:32787735
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:13176 Homo sapiens (human) 10320 IKZF1
  • PMID:22699455
DOID:9256 colorectal cancer HGNC:13176 Homo sapiens (human) 10320 IKZF1
  • PMID:21737484
  • PMID:25928810
  • PMID:27726312
  • PMID:29780264
  • PMID:29796114
  • PMID:29992492
  • PMID:31010820
  • PMID:31320627
  • PMID:31909823
  • PMID:32958500
  • PMID:33478584
  • PMID:33723131
DOID:9952 acute lymphoblastic leukemia HGNC:13176 Homo sapiens (human) 10320 IKZF1
  • PMID:24786325
DOID:684 hepatocellular carcinoma HGNC:13176 Homo sapiens (human) 10320 IKZF1
  • PMID:25301737
DOID:0081155 common variable immunodeficiency 13 HGNC:13176 Homo sapiens (human) 10320 IKZF1
  • RGD:7240710
DOID:0060041 autism spectrum disorder HGNC:6494 Homo sapiens (human) 10319 LAMC3
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:920 Homo sapiens (human) 10317 B3GALT5
  • PMID:14555842
DOID:9970 obesity HGNC:4518 Homo sapiens (human) 10316 NMUR1
  • MGI:6194238
DOID:0110765 hereditary spastic paraplegia 12 HGNC:10469 Homo sapiens (human) 10313 RTN3
  • MGI:6194238
DOID:2476 hereditary spastic paraplegia HGNC:10469 Homo sapiens (human) 10313 RTN3
  • MGI:6194238
DOID:0112236 lissencephaly 6 HGNC:6217 Homo sapiens (human) 10300 KATNB1
  • RGD:7240710
DOID:10907 microcephaly HGNC:6217 Homo sapiens (human) 10300 KATNB1
  • MGI:6194238
DOID:0060250 idiopathic scoliosis HGNC:6217 Homo sapiens (human) 10300 KATNB1
  • MGI:6194238
DOID:0060257 dyschromatosis symmetrica hereditaria HGNC:225 Homo sapiens (human) 103 ADAR
  • PMID:12916015
  • PMID:15955093
  • RGD:7240710
DOID:5082 liver cirrhosis HGNC:225 Homo sapiens (human) 103 ADAR
  • PMID:29018269
DOID:11166 Human papillomavirus infectious disease HGNC:225 Homo sapiens (human) 103 ADAR
  • PMID:31882741
DOID:0050629 Aicardi-Goutieres syndrome HGNC:225 Homo sapiens (human) 103 ADAR
  • MGI:6194238
  • PMID:23001123
  • RGD:7240710
DOID:10534 stomach cancer HGNC:225 Homo sapiens (human) 103 ADAR
  • PMID:30563560
DOID:3744 cervical squamous cell carcinoma HGNC:225 Homo sapiens (human) 103 ADAR
  • PMID:28109322
DOID:14330 Parkinson's disease HGNC:16059 Homo sapiens (human) 10298 PAK4
  • MGI:6194238
DOID:4467 clear cell renal cell carcinoma HGNC:16059 Homo sapiens (human) 10298 PAK4
  • PMID:25744653

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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