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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 July 29, 2024
Displaying entries 7051 - 7075 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:289 endometriosis HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • PMID:18849443
DOID:4372 intracranial embolism HGNC:6344 Homo sapiens (human) 9365 KL
  • PMID:16973281
DOID:8947 diabetic retinopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:11106834
  • PMID:2157294
  • PMID:23065222
  • PMID:7729604
DOID:8947 diabetic retinopathy HGNC:8978 Homo sapiens (human) 5294 PIK3CG
  • MGI:6194238
DOID:1470 major depressive disorder HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • MGI:6194238
  • PMID:1570017
  • PMID:8200206
  • PMID:8314445
  • PMID:8325445
  • RGD:7240710
DOID:289 endometriosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:15714130
  • PMID:19068087
DOID:1612 breast cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:17764565
  • PMID:8673923
DOID:2752 glycogen storage disease II HGNC:4065 Homo sapiens (human) 2548 GAA
  • MGI:6194238
  • RGD:7240710
DOID:26 pancreas disease HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:19843662
DOID:0050433 fatal familial insomnia HGNC:9449 Homo sapiens (human) 5621 PRNP
  • MGI:6194238
  • RGD:7240710
DOID:5614 eye disease HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:16146574
DOID:2043 hepatitis B HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:16231358
DOID:552 pneumonia HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20302606
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:23269818
DOID:0050700 cardiomyopathy HGNC:18859 Homo sapiens (human) 56848 SPHK2
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 HGNC:19139 Homo sapiens (human) 55624 POMGNT1
  • MGI:6194238
DOID:1024 leprosy HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:17548585
  • RGD:7240710
DOID:0050563 nonsyndromic deafness HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:0070162 hereditary sensory and autonomic neuropathy type 1 HGNC:11277 Homo sapiens (human) 10558 SPTLC1
  • MGI:6194238
DOID:2841 asthma HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:15316498
  • PMID:17573729
  • PMID:18489027
  • PMID:19862936
DOID:6432 pulmonary hypertension HGNC:4819 Homo sapiens (human) 3037 HAS2
  • MGI:6194238
DOID:5520 head and neck squamous cell carcinoma HGNC:2623 Homo sapiens (human) 1559 CYP2C9
  • PMID:19954746
DOID:3534 Lafora disease HGNC:4707 Homo sapiens (human) 2998 GYS2
  • MGI:6194238

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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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