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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 61601 - 61625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:10591 pre-eclampsia HGNC:2228 Homo sapiens (human) 1312 COMT
  • MGI:6194238
DOID:9974 drug dependence HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:31150143
DOID:13078 eumycotic mycetoma HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:20184498
DOID:127 leiomyoma HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:16443508
  • PMID:16730007
DOID:1612 breast cancer HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:15285606
  • PMID:17429315
  • PMID:17507616
  • PMID:17562079
DOID:4676 uremia HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:7437264
DOID:1324 lung cancer HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:27644662
DOID:1380 endometrial cancer HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:12810635
  • PMID:15285606
  • PMID:17442187
DOID:2559 opiate dependence HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:27061230
  • PMID:32407152
DOID:0060001 withdrawal disorder HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:11900601
DOID:0070303 multiple epiphyseal dysplasia 1 HGNC:2227 Homo sapiens (human) 1311 COMP
  • RGD:7240710
DOID:0080047 pseudoachondroplasia HGNC:2227 Homo sapiens (human) 1311 COMP
  • MGI:6194238
  • RGD:7240710
DOID:0070467 carpal tunnel syndrome 2 HGNC:2227 Homo sapiens (human) 1311 COMP
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:2227 Homo sapiens (human) 1311 COMP
  • PMID:7670471
  • PMID:7670472
DOID:12721 multiple epiphyseal dysplasia HGNC:2227 Homo sapiens (human) 1311 COMP
  • MGI:6194238
DOID:0112315 brain small vessel disease 3 HGNC:26182 Homo sapiens (human) 79709 COLGALT1
  • RGD:7240710
DOID:674 cleft palate HGNC:17213 Homo sapiens (human) 78989 COLEC11
  • MGI:6194238
DOID:0060576 3MC syndrome 2 HGNC:17213 Homo sapiens (human) 78989 COLEC11
  • RGD:7240710
DOID:0060577 3MC syndrome 3 HGNC:2220 Homo sapiens (human) 10584 COLEC10
  • RGD:7240710
DOID:0070304 multiple epiphyseal dysplasia 3 HGNC:2219 Homo sapiens (human) 1299 COL9A3
  • RGD:7240710
DOID:0080046 Stickler syndrome HGNC:2219 Homo sapiens (human) 1299 COL9A3
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:2219 Homo sapiens (human) 1299 COL9A3
  • PMID:10090888
DOID:0080046 Stickler syndrome HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • RGD:7240710
DOID:2256 osteochondrodysplasia HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • PMID:8528240
DOID:0070298 multiple epiphyseal dysplasia 2 HGNC:2218 Homo sapiens (human) 1298 COL9A2
  • RGD:7240710

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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