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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 6026 - 6050 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:14330 Parkinson's disease HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:17362997
  • PMID:21767974
DOID:1793 pancreatic cancer HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:12499913
DOID:0080433 developmental and epileptic encephalopathy 51 HGNC:6971 Homo sapiens (human) 4191 MDH2
  • MGI:6194238
  • RGD:7240710
DOID:0112263 hypoinsulinemic hypoglycemia with hemihypertrophy HGNC:392 Homo sapiens (human) 208 AKT2
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:2666 Homo sapiens (human) 1605 DAG1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:0070341 neonatal-onset type II citrullinemia HGNC:10983 Homo sapiens (human) 10165 SLC25A13
  • RGD:7240710
DOID:1380 endometrial cancer HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:18497059
DOID:3459 breast carcinoma HGNC:9065 Homo sapiens (human) 5335 PLCG1
  • PMID:1683701
DOID:0081292 traumatic brain injury HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:4676 uremia HGNC:438 Homo sapiens (human) 249 ALPL
  • MGI:6194238
DOID:10763 hypertension HGNC:4553 Homo sapiens (human) 2876 GPX1
  • MGI:6194238
  • PMID:17198913
DOID:3907 lung squamous cell carcinoma HGNC:2597 Homo sapiens (human) 1545 CYP1B1
  • PMID:10739169
DOID:11650 bronchopulmonary dysplasia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20558631
DOID:11054 urinary bladder cancer HGNC:451 Homo sapiens (human) 23600 AMACR
  • PMID:18648853
DOID:13129 severe pre-eclampsia HGNC:587 Homo sapiens (human) 328 APEX1
  • PMID:24619222
DOID:3770 pulmonary fibrosis HGNC:10802 Homo sapiens (human) 6440 SFTPC
  • PMID:20656946
DOID:0080322 polycystic kidney disease HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:0060639 permanent neonatal diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • RGD:7240710
DOID:3068 glioblastoma HGNC:8976 Homo sapiens (human) 5291 PIK3CB
  • PMID:21188471
  • PMID:26956052
DOID:3393 coronary artery disease HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • PMID:31377187
DOID:10629 microphthalmia HGNC:6697 Homo sapiens (human) 4041 LRP5
  • PMID:28111184
DOID:9352 type 2 diabetes mellitus HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • PMID:16025115
  • RGD:7240710
DOID:2237 hepatitis HGNC:8125 Homo sapiens (human) 4968 OGG1
  • MGI:6194238
DOID:9675 pulmonary emphysema HGNC:4019 Homo sapiens (human) 2530 FUT8
  • 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