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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 October 9, 2024
Displaying entries 71551 - 71575 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:6000 congestive heart failure HGNC:7940 Homo sapiens (human) 4879 NPPB
  • MGI:6194238
  • PMID:11421854
  • PMID:17257273
  • PMID:2143809
DOID:0060692 platelet-type bleeding disorder 8 MGI:1918089 Mus musculus (house mouse) 70839 P2ry12
  • MGI:6194238
  • PMID:11413167
  • PMID:12897207
DOID:0050773 paraganglioma HGNC:10681 Homo sapiens (human) 6390 SDHB
  • MGI:6194238
  • PMID:11404820
  • RGD:7240710
DOID:2841 asthma HGNC:6015 Homo sapiens (human) 3566 IL4R
  • MGI:6194238
  • PMID:11398072
  • PMID:11709756
  • PMID:12133990
  • PMID:12940513
  • PMID:15479272
  • PMID:16917945
  • PMID:17170387
  • PMID:17586032
  • PMID:17823973
  • PMID:18425216
  • PMID:20868478
DOID:10825 essential hypertension HGNC:7876 Homo sapiens (human) 4846 NOS3
  • MGI:6194238
  • PMID:11394896
  • PMID:9084930
DOID:5844 myocardial infarction HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
  • PMID:11393670
  • PMID:17299437
DOID:0110154 Charcot-Marie-Tooth disease type 2A1 HGNC:16636 Homo sapiens (human) 23095 KIF1B
  • MGI:6194238
  • PMID:11389829
  • RGD:7240710
DOID:2734 keratosis follicularis MGI:88110 Mus musculus (house mouse) 11938 Atp2a2
  • MGI:6194238
  • PMID:11389134
DOID:9352 type 2 diabetes mellitus MGI:104874 Mus musculus (house mouse) 11652 Akt2
  • MGI:6194238
  • PMID:11387480
DOID:1856 cherubism HGNC:10825 Homo sapiens (human) 6452 SH3BP2
  • MGI:6194238
  • PMID:11381256
  • RGD:7240710
DOID:2339 Crouzon syndrome HGNC:3689 Homo sapiens (human) 2263 FGFR2
  • MGI:6194238
  • PMID:11380921
  • PMID:11711827
  • PMID:7874170
  • PMID:7987400
  • RGD:7240710
DOID:10584 retinitis pigmentosa HGNC:2151 Homo sapiens (human) 1258 CNGB1
  • MGI:6194238
  • PMID:11379879
DOID:10652 Alzheimer's disease MGI:97004 Mus musculus (house mouse) 17380 Mme
  • MGI:6194238
  • PMID:11375493
DOID:8947 diabetic retinopathy HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
  • PMID:11375354
  • PMID:14704946
  • PMID:16969646
  • PMID:19542745
  • PMID:22116960
  • PMID:22427038
  • PMID:22475522
  • PMID:23091285
DOID:0080092 myofibrillar myopathy 1 MGI:94885 Mus musculus (house mouse) 13346 Des
  • MGI:6194238
  • PMID:11352891
  • PMID:25394388
  • PMID:8794866
DOID:6000 congestive heart failure RGD:621320 Rattus norvegicus (Norway rat) 81687 Mmp9
  • MGI:6194238
  • PMID:11342481
  • PMID:17913382
DOID:3021 acute kidney failure RGD:2542 Rattus norvegicus (Norway rat) 25313 Egf
  • MGI:6194238
  • PMID:11340354
DOID:9352 type 2 diabetes mellitus RGD:2689 Rattus norvegicus (Norway rat) 25024 Gipr
  • MGI:6194238
  • PMID:11334402
DOID:0070255 congenital disorder of glycosylation type IIc HGNC:20197 Homo sapiens (human) 55343 SLC35C1
  • MGI:6194238
  • PMID:11326280
  • RGD:7240710
DOID:1324 lung cancer MGI:96680 Mus musculus (house mouse) 16653 Kras
  • MGI:6194238
  • PMID:11323676
  • PMID:18493606
  • PMID:20609353
  • PMID:21512139
  • PMID:21514245
  • PMID:24239348
  • PMID:24430184
DOID:9970 obesity HGNC:4923 Homo sapiens (human) 3099 HK2
  • MGI:6194238
  • PMID:11319725
DOID:0050638 transthyretin amyloidosis MGI:98865 Mus musculus (house mouse) 22139 Ttr
  • MGI:6194238
  • PMID:11310831
  • PMID:29360446
DOID:1919 Lesch-Nyhan syndrome MGI:96217 Mus musculus (house mouse) 15452 Hprt1
  • MGI:6194238
  • PMID:11297820
  • PMID:7509865
DOID:9119 acute myeloid leukemia HGNC:3765 Homo sapiens (human) 2322 FLT3
  • MGI:6194238
  • PMID:11290608
  • PMID:11442493
  • PMID:16642044
  • PMID:23969938
  • PMID:8562934
  • RGD:7240710
DOID:4603 epidermolytic hyperkeratosis HGNC:6412 Homo sapiens (human) 3848 KRT1
  • MGI:6194238
  • PMID:11286616
  • RGD:7240710

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024