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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 6451 - 6475 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060774 congenital diarrhea HGNC:16526 Homo sapiens (human) 51703 ACSL5
  • RGD:7240710
DOID:13564 aspergillosis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:16461792
DOID:9256 colorectal cancer HGNC:19877 Homo sapiens (human) 79695 GALNT12
  • RGD:7240710
DOID:4195 hyperglycemia HGNC:6535 Homo sapiens (human) 3939 LDHA
  • MGI:6194238
DOID:5723 optic atrophy HGNC:19691 Homo sapiens (human) 51102 MECR
  • RGD:7240710
DOID:552 pneumonia HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:399 tuberculosis HGNC:11847 Homo sapiens (human) 7096 TLR1
  • PMID:18091991
DOID:5199 ureteral obstruction HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:1097 Homo sapiens (human) 673 BRAF
  • RGD:7240710
DOID:2945 severe acute respiratory syndrome HGNC:5993 Homo sapiens (human) 3554 IL1R1
  • PMID:19635508
DOID:289 endometriosis HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • MGI:6194238
  • PMID:8550748
DOID:1923 disorder of sexual development HGNC:5212 Homo sapiens (human) 3293 HSD17B3
  • PMID:8075637
DOID:5082 liver cirrhosis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:28650518
DOID:9352 type 2 diabetes mellitus HGNC:9281 Homo sapiens (human) 5499 PPP1CA
  • MGI:6194238
DOID:1936 atherosclerosis HGNC:10721 Homo sapiens (human) 6403 SELP
  • MGI:6194238
DOID:1520 colon carcinoma HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:29940770
DOID:0080546 non-alcoholic fatty liver HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • PMID:33081272
DOID:11054 urinary bladder cancer HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:23142523
DOID:0080596 hyper IgE recurrent infection syndrome 4 HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:10571 Homo sapiens (human) 6319 SCD
  • MGI:6194238
DOID:13406 pulmonary sarcoidosis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:20813038
DOID:0111230 congenital muscular dystrophy-dystroglycanopathy type A11 HGNC:28596 Homo sapiens (human) 148789 B3GALNT2
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:19644070
DOID:13976 peptic esophagitis HGNC:9599 Homo sapiens (human) 9536 PTGES
  • MGI:6194238
DOID:0080199 colorectal carcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:30469315

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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