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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 10551 - 10575 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:8619 recurrent hypersomnia HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:19404393
DOID:8986 narcolepsy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:18820697
DOID:9884 muscular dystrophy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:21665002
DOID:10907 microcephaly HGNC:1938 Homo sapiens (human) 1120 CHKB
  • MGI:6194238
DOID:0110632 megaconial type congenital muscular dystrophy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • MGI:6194238
  • RGD:7240710
DOID:1059 intellectual disability HGNC:1938 Homo sapiens (human) 1120 CHKB
  • PMID:21665002
DOID:1826 epilepsy HGNC:1938 Homo sapiens (human) 1120 CHKB
  • MGI:6194238
DOID:1826 epilepsy HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:219 colon cancer HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:10907 microcephaly HGNC:1937 Homo sapiens (human) 1119 CHKA
  • MGI:6194238
DOID:0050912 colon adenoma HGNC:1937 Homo sapiens (human) 1119 CHKA
  • PMID:10363580
DOID:2841 asthma HGNC:17432 Homo sapiens (human) 27159 CHIA
  • PMID:15192232
  • PMID:16179638
  • PMID:20226308
DOID:12053 cryptococcosis HGNC:17432 Homo sapiens (human) 27159 CHIA
  • MGI:6194238
DOID:0050127 sinusitis HGNC:17432 Homo sapiens (human) 27159 CHIA
  • PMID:19379605
DOID:10325 silicosis HGNC:17432 Homo sapiens (human) 27159 CHIA
  • MGI:6194238
DOID:1909 melanoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:16456816
DOID:2349 arteriosclerosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:10073974
DOID:3083 chronic obstructive pulmonary disease HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20656949
DOID:13406 pulmonary sarcoidosis HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:15763444
DOID:0080199 colorectal carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12124825
DOID:11650 bronchopulmonary dysplasia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:20558631
DOID:6000 congestive heart failure HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:19961288
DOID:0050685 small cell carcinoma HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:15541818
DOID:5419 schizophrenia HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • RGD:7240710

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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