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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 69376 - 69400 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:3393 coronary artery disease HGNC:7155 Homo sapiens (human) 4312 MMP1
  • PMID:15619398
  • PMID:17893005
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:8869 neuromyelitis optica HGNC:637 Homo sapiens (human) 361 AQP4
  • PMID:16087714
  • PMID:18420727
  • PMID:20047900
  • PMID:23116879
  • PMID:23890015
DOID:9970 obesity HGNC:12519 Homo sapiens (human) 7352 UCP3
  • PMID:12145158
  • PMID:18249216
  • PMID:9700198
  • PMID:9769326
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:983 Homo sapiens (human) 590 BCHE
  • PMID:11793025
  • PMID:16442234
DOID:9074 systemic lupus erythematosus HGNC:3535 Homo sapiens (human) 2147 F2
  • PMID:20807656
  • PMID:21239755
DOID:10923 sickle cell anemia HGNC:13221 Homo sapiens (human) 53335 BCL11A
  • PMID:18667698
  • PMID:22360576
DOID:2957 pulmonary tuberculosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18212516
  • PMID:20650298
DOID:2841 asthma HGNC:286 Homo sapiens (human) 154 ADRB2
  • PMID:1655856
  • PMID:18569231
  • PMID:18785519
  • PMID:19029431
  • PMID:19638684
  • PMID:19800676
  • PMID:20004781
  • PMID:20443840
DOID:0060022 CD40 ligand deficiency HGNC:11935 Homo sapiens (human) 959 CD40LG
  • PMID:15358621
  • PMID:16508335
  • PMID:17553565
  • PMID:21841160
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:22930375
  • PMID:26823947
  • PMID:26950655
DOID:9675 pulmonary emphysema HGNC:8941 Homo sapiens (human) 5265 SERPINA1
  • PMID:19941265
  • PMID:21030517
DOID:5844 myocardial infarction HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:10428310
  • PMID:20176799
DOID:0050741 alcohol dependence HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:10698363
  • PMID:11244495
  • PMID:16499480
  • PMID:16648777
  • PMID:16984965
  • PMID:20517217
  • PMID:20860878
  • PMID:22208661
  • PMID:24390676
  • PMID:25035107
  • PMID:25491588
  • PMID:31150143
DOID:2394 ovarian cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:10493953
DOID:12241 beta thalassemia HGNC:13221 Homo sapiens (human) 53335 BCL11A
  • PMID:22258351
  • PMID:23541515
  • PMID:25574177
  • PMID:25751242
DOID:1485 cystic fibrosis HGNC:7218 Homo sapiens (human) 4353 MPO
  • PMID:16883063
  • PMID:20954832
DOID:10003 sensorineural hearing loss HGNC:3535 Homo sapiens (human) 2147 F2
  • PMID:16572609
  • PMID:17334320
  • PMID:18636032
DOID:8924 autoimmune thrombocytopenic purpura HGNC:3618 Homo sapiens (human) 2213 FCGR2B
  • PMID:15566359
  • PMID:19549396
  • PMID:21131591
DOID:9256 colorectal cancer HGNC:4585 Homo sapiens (human) 2903 GRIN2A
  • PMID:17922030
  • PMID:33106877
DOID:0080597 Kleefstra syndrome HGNC:24650 Homo sapiens (human) 79813 EHMT1
  • PMID:21538692
  • PMID:21910222
DOID:5419 schizophrenia HGNC:2228 Homo sapiens (human) 1312 COMT
  • PMID:12402217
  • PMID:16984965
  • PMID:19881467
  • PMID:26255563
DOID:7693 abdominal aortic aneurysm HGNC:7159 Homo sapiens (human) 4322 MMP13
  • PMID:15156361
  • PMID:15944607
DOID:11934 head and neck cancer HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:16721740
  • PMID:20846153
DOID:1793 pancreatic cancer HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:19152242
  • PMID:19375425
  • PMID:19572116

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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