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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 70601 - 70625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:0111425 restrictive cardiomyopathy 1 HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • RGD:7240710
DOID:0112380 muscular dystrophy-dystroglycanopathy type B2 HGNC:19743 Homo sapiens (human) 29954 POMT2
  • RGD:7240710
DOID:0080283 developmental and epileptic encephalopathy 55 HGNC:3046 Homo sapiens (human) 51227 PIGP
  • RGD:7240710
DOID:0111740 X-linked deafness 6 HGNC:2208 Homo sapiens (human) 1288 COL4A6
  • RGD:7240710
DOID:0110965 brachydactyly type A2 HGNC:1069 Homo sapiens (human) 650 BMP2
  • RGD:7240710
DOID:0081190 autosomal recessive intellectual developmental disorder 18 HGNC:2372 Homo sapiens (human) 9439 MED23
  • RGD:7240710
DOID:0110444 dilated cardiomyopathy 1X HGNC:3622 Homo sapiens (human) 2218 FKTN
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:15632 Homo sapiens (human) 51311 TLR8
  • RGD:7240710
DOID:0070268 congenital disorder of glycosylation type IIp HGNC:18085 Homo sapiens (human) 147007 TMEM199
  • RGD:7240710
DOID:0081212 autosomal recessive intellectual developmental disorder 48 HGNC:31399 Homo sapiens (human) 388662 SLC6A17
  • RGD:7240710
DOID:0070454 hereditary spastic paraplegia 70 HGNC:6898 Homo sapiens (human) 4141 MARS1
  • RGD:7240710
DOID:0110026 age related macular degeneration 14 HGNC:1248 Homo sapiens (human) 717 C2
  • RGD:7240710
DOID:0081344 congenital myopathy 9B HGNC:4023 Homo sapiens (human) 8087 FXR1
  • RGD:7240710
DOID:0060746 basal laminar drusen HGNC:4883 Homo sapiens (human) 3075 CFH
  • RGD:7240710
DOID:0081226 autosomal recessive intellectual developmental disorder 65 HGNC:18039 Homo sapiens (human) 10765 KDM5B
  • RGD:7240710
DOID:9410 panhypopituitarism HGNC:10249 Homo sapiens (human) 6091 ROBO1
  • RGD:7240710
DOID:0112187 thyroid dyshormonogenesis 3 HGNC:11764 Homo sapiens (human) 7038 TG
  • RGD:7240710
DOID:0080688 mosaic variegated aneuploidy syndrome HGNC:17814 Homo sapiens (human) 55719 SLF2
  • RGD:7240710
DOID:3969 thyroid gland papillary carcinoma HGNC:7102 Homo sapiens (human) 9562 MINPP1
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:10830 Homo sapiens (human) 6455 SH3GL1
  • RGD:7240710
DOID:0060668 anencephaly HGNC:29558 Homo sapiens (human) 81788 NUAK2
  • RGD:7240710
DOID:0050646 distal arthrogryposis HGNC:16305 Homo sapiens (human) 170689 ADAMTS15
  • RGD:7240710
DOID:0110013 advanced sleep phase syndrome 3 HGNC:8847 Homo sapiens (human) 8863 PER3
  • RGD:7240710
DOID:4253 melorheostosis HGNC:6840 Homo sapiens (human) 5604 MAP2K1
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6882 Homo sapiens (human) 9479 MAPK8IP1
  • RGD:7240710

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

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


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