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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 62201 - 62225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:3908 lung non-small cell carcinoma HGNC:1957 Homo sapiens (human) 1136 CHRNA3
  • PMID:21747048
  • PMID:22722785
DOID:0050741 alcohol dependence HGNC:1957 Homo sapiens (human) 1136 CHRNA3
  • PMID:24057674
DOID:3083 chronic obstructive pulmonary disease HGNC:1957 Homo sapiens (human) 1136 CHRNA3
  • PMID:22441734
  • PMID:23056235
  • PMID:23207642
  • PMID:26751916
  • PMID:29993116
DOID:0060685 autosomal dominant nocturnal frontal lobe epilepsy 4 HGNC:1956 Homo sapiens (human) 1135 CHRNA2
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:1956 Homo sapiens (human) 1135 CHRNA2
  • MGI:6194238
DOID:3635 congenital myasthenic syndrome HGNC:1956 Homo sapiens (human) 1135 CHRNA2
  • MGI:6194238
DOID:0081119 benign familial infantile seizures 6 HGNC:1956 Homo sapiens (human) 1135 CHRNA2
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:1955 Homo sapiens (human) 1134 CHRNA1
  • MGI:6194238
DOID:3635 congenital myasthenic syndrome HGNC:1955 Homo sapiens (human) 1134 CHRNA1
  • MGI:6194238
DOID:0110662 congenital myasthenic syndrome 1B HGNC:1955 Homo sapiens (human) 1134 CHRNA1
  • RGD:7240710
DOID:0110663 congenital myasthenic syndrome 1A HGNC:1955 Homo sapiens (human) 1134 CHRNA1
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:1953 Homo sapiens (human) 1132 CHRM4
  • MGI:6194238
DOID:2841 asthma HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • PMID:20394512
DOID:3083 chronic obstructive pulmonary disease HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • PMID:19281093
DOID:0060610 megacystis-microcolon-intestinal hypoperistalsis syndrome HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • MGI:6194238
DOID:365 bladder disease HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • PMID:17922784
DOID:0060889 prune belly syndrome HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • RGD:7240710
DOID:0050685 small cell carcinoma HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • PMID:20150622
DOID:3770 pulmonary fibrosis HGNC:1952 Homo sapiens (human) 1131 CHRM3
  • PMID:18480105
DOID:1596 depressive disorder HGNC:1951 Homo sapiens (human) 1129 CHRM2
  • MGI:6194238
DOID:2841 asthma HGNC:1951 Homo sapiens (human) 1129 CHRM2
  • PMID:19308904
DOID:3312 bipolar disorder HGNC:1951 Homo sapiens (human) 1129 CHRM2
  • PMID:19103464
  • PMID:20351719
DOID:12140 Chagas disease HGNC:1951 Homo sapiens (human) 1129 CHRM2
  • PMID:9148906
DOID:5419 schizophrenia HGNC:1951 Homo sapiens (human) 1129 CHRM2
  • PMID:20691427
DOID:9976 heroin dependence HGNC:1951 Homo sapiens (human) 1129 CHRM2
  • PMID:19500151

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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