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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 7901 - 7925 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3454 brain infarction HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:3083 chronic obstructive pulmonary disease HGNC:10803 Homo sapiens (human) 6441 SFTPD
  • PMID:18310480
  • PMID:19797132
  • PMID:20075511
  • PMID:20448057
DOID:9352 type 2 diabetes mellitus HGNC:5209 Homo sapiens (human) 3291 HSD11B2
  • PMID:17519316
DOID:0060076 estrogen-receptor negative breast cancer HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:26351264
DOID:10591 pre-eclampsia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:18054022
DOID:10609 rickets HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
  • PMID:9486994
DOID:11832 visual epilepsy HGNC:3353 Homo sapiens (human) 2026 ENO2
  • MGI:6194238
DOID:3073 brain glioblastoma multiforme HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:20219118
DOID:0080737 Ehlers-Danlos syndrome musculocontractural type 2 HGNC:21144 Homo sapiens (human) 29940 DSE
  • RGD:7240710
DOID:3602 toxic encephalopathy HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238
DOID:4947 cholangiocarcinoma HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:12031086
DOID:2871 endometrial carcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:16144912
DOID:4194 glucose metabolism disease HGNC:4922 Homo sapiens (human) 3098 HK1
  • MGI:6194238
DOID:0081183 autosomal recessive intellectual developmental disorder 7 HGNC:30242 Homo sapiens (human) 7991 TUSC3
  • RGD:7240710
DOID:1184 nephrotic syndrome HGNC:11178 Homo sapiens (human) 8435 SOAT2
  • MGI:6194238
DOID:9743 diabetic neuropathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:14115 toxic shock syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:1612 breast cancer HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:16019138
DOID:11476 osteoporosis HGNC:8729 Homo sapiens (human) 5111 PCNA
  • MGI:6194238
DOID:10457 Legionnaires' disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19073229
DOID:0050625 biliary tract benign neoplasm HGNC:7413 Homo sapiens (human) 4507 MTAP
  • PMID:16373701
DOID:1596 depressive disorder HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • MGI:6194238
DOID:1380 endometrial cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:18348659
DOID:1793 pancreatic cancer HGNC:7371 Homo sapiens (human) 10232 MSLN
  • PMID:17019794
  • PMID:17785569
  • PMID:18281514
  • PMID:19843662
DOID:9269 maple syrup urine disease HGNC:2698 Homo sapiens (human) 1629 DBT
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024