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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 67526 - 67550 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:5426 primary ovarian insufficiency HGNC:17675 Homo sapiens (human) 57510 XPO5
  • PMID:23549446
DOID:0112251 Ghosal hematodiaphyseal syndrome HGNC:11609 Homo sapiens (human) 6916 TBXAS1
  • RGD:7240710
DOID:9669 senile cataract HGNC:5233 Homo sapiens (human) 3304 HSPA1B
  • PMID:23666708
DOID:9993 hypoglycemia HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:9435328
DOID:0070296 primary autosomal recessive microcephaly HGNC:6637 Homo sapiens (human) 4001 LMNB1
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:9645 Homo sapiens (human) 5782 PTPN12
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:18437 Homo sapiens (human) 84868 HAVCR2
  • PMID:22472081
DOID:0111726 geleophysic dysplasia 2 HGNC:3603 Homo sapiens (human) 2200 FBN1
  • RGD:7240710
DOID:10763 hypertension HGNC:7200 Homo sapiens (human) 4343 MOV10
  • PMID:24338417
DOID:5295 intestinal disease HGNC:1076 Homo sapiens (human) 657 BMPR1A
  • PMID:11381269
  • PMID:16525031
  • PMID:16685657
DOID:12236 primary biliary cholangitis HGNC:11365 Homo sapiens (human) 6775 STAT4
  • PMID:24648611
  • PMID:26084578
  • PMID:28395724
DOID:9164 achalasia HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1
  • PMID:11837716
  • PMID:30092016
  • PMID:30788115
DOID:2841 asthma HGNC:23064 Homo sapiens (human) 119391 GSTO2
  • PMID:20374258
DOID:0112167 autosomal dominant nonsyndromic deafness 76 HGNC:9090 Homo sapiens (human) 5357 PLS1
  • RGD:7240710
DOID:13025 retinopathy of prematurity HGNC:7876 Homo sapiens (human) 4846 NOS3
  • PMID:18334945
DOID:12849 autistic disorder HGNC:13875 Homo sapiens (human) 93986 FOXP2
  • PMID:12116195
  • PMID:12655497
  • PMID:15108192
  • PMID:15737702
  • PMID:15998549
DOID:3393 coronary artery disease HGNC:3616 Homo sapiens (human) 2212 FCGR2A
  • PMID:20973705
DOID:5082 liver cirrhosis HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1
  • PMID:17845309
  • PMID:23321320
DOID:0080533 Carney-Stratakis syndrome HGNC:10682 Homo sapiens (human) 6391 SDHC
  • RGD:7240710
DOID:3805 porokeratosis HGNC:3631 Homo sapiens (human) 2224 FDPS
  • RGD:7240710
DOID:1070 primary open angle glaucoma HGNC:11785 Homo sapiens (human) 7057 THBS1
  • PMID:34143713
DOID:1793 pancreatic cancer HGNC:795 Homo sapiens (human) 472 ATM
  • PMID:16520463
  • PMID:18381943
  • PMID:19147782
DOID:0080722 Kenny-Caffey syndrome type 1 HGNC:11582 Homo sapiens (human) 6905 TBCE
  • RGD:7240710
DOID:1059 intellectual disability HGNC:6407 Homo sapiens (human) 3845 KRAS
  • PMID:17056636
DOID:10763 hypertension RGD:61925 Rattus norvegicus (Norway rat) 29340 Prkce
  • PMID:15792354

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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