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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 January 28, 2025
Displaying entries 13201 - 13225 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▼ References
DOID:3911 progeria MGI:1917925 Mus musculus (house mouse) 70675 Vcpip1 author statement supported by traceable reference
  • PMID:32649882
DOID:2729 dyskeratosis congenita MGI:1861727 Mus musculus (house mouse) 245474 Dkc1 author statement supported by traceable reference
  • PMID:12522253
  • PMID:21241452
DOID:0050475 Weill-Marchesani syndrome MGI:95489 Mus musculus (house mouse) 14118 Fbn1 author statement supported by traceable reference
  • PMID:22242013
DOID:0110928 nemaline myopathy 2 MGI:97292 Mus musculus (house mouse) 17996 Neb author statement supported by traceable reference
  • PMID:19346529
  • PMID:23715096
  • PMID:26123491
  • PMID:32066503
DOID:0060684 autosomal dominant nocturnal frontal lobe epilepsy 3 MGI:87891 Mus musculus (house mouse) 11444 Chrnb2 author statement supported by traceable reference
  • PMID:19153075
  • PMID:20603624
DOID:0014667 disease of metabolism MGI:99511 Mus musculus (house mouse) 19247 Ptpn11 author statement supported by traceable reference
  • PMID:19001090
DOID:11836 clubfoot MGI:1921303 Mus musculus (house mouse) 74053 Grip1 author statement supported by traceable reference
  • MGI:61605
DOID:12388 neurohypophyseal diabetes insipidus MGI:88121 Mus musculus (house mouse) 11998 Avp author statement supported by traceable reference
  • PMID:14660745
  • PMID:19297548
DOID:9521 Laron syndrome MGI:95708 Mus musculus (house mouse) 14600 Ghr author statement supported by traceable reference
  • PMID:11133160
  • PMID:19269870
  • PMID:9371826
DOID:10754 otitis media MGI:107718 Mus musculus (house mouse) 110082 Dnah5 author statement supported by traceable reference
  • PMID:11912187
DOID:0111029 hemochromatosis type 1 MGI:109191 Mus musculus (house mouse) 15216 Hfe author statement supported by traceable reference
  • PMID:10381492
  • PMID:10557317
  • PMID:10791995
  • PMID:14673107
  • PMID:16491649
  • PMID:17264297
  • PMID:20976594
DOID:0110545 autosomal dominant nonsyndromic deafness 13 MGI:88447 Mus musculus (house mouse) 12815 Col11a2 author statement supported by traceable reference
  • PMID:11668593
DOID:13544 low tension glaucoma MGI:105083 Mus musculus (house mouse) 20510 Slc1a1 author statement supported by traceable reference
  • PMID:17607354
DOID:3652 Leigh disease MGI:1343135 Mus musculus (house mouse) 17993 Ndufs4 author statement supported by traceable reference
  • PMID:20534480
  • PMID:22653057
DOID:0060581 Noonan syndrome 3 MGI:96680 Mus musculus (house mouse) 16653 Kras author statement supported by traceable reference
  • PMID:25359213
DOID:0050433 fatal familial insomnia MGI:97769 Mus musculus (house mouse) 19122 Prnp author statement supported by traceable reference
  • PMID:19709627
  • PMID:23959875
DOID:11633 thyroid hormone resistance syndrome MGI:1276523 Mus musculus (house mouse) 17977 Ncoa1 author statement supported by traceable reference
  • PMID:10202153
DOID:0110266 cataract 9 multiple types MGI:88515 Mus musculus (house mouse) 12954 Cryaa author statement supported by traceable reference
  • PMID:11687536
  • PMID:18056999
  • PMID:19619312
  • PMID:8812430
  • PMID:9023351
DOID:2512 nevoid basal cell carcinoma syndrome MGI:105373 Mus musculus (house mouse) 19206 Ptch1 author statement supported by traceable reference
  • PMID:12542834
  • PMID:23897749
  • PMID:9262482
  • PMID:9585239
DOID:0110657 congenital myasthenic syndrome 8 MGI:87961 Mus musculus (house mouse) 11603 Agrn author statement supported by traceable reference
  • PMID:21890498
DOID:14705 Pfeiffer syndrome MGI:95522 Mus musculus (house mouse) 14182 Fgfr1 author statement supported by traceable reference
  • PMID:21538817
  • PMID:8001823
DOID:10140 dry eye syndrome MGI:103151 Mus musculus (house mouse) 18830 Pltp author statement supported by traceable reference
  • PMID:21514421
DOID:0060713 autosomal recessive congenital ichthyosis 4B MGI:1923810 Mus musculus (house mouse) 76560 Prss8 author statement supported by traceable reference
  • PMID:16061697
DOID:14780 KBG syndrome MGI:1924337 Mus musculus (house mouse) 77087 Ankrd11 author statement supported by traceable reference
  • PMID:33996804
DOID:0060480 left ventricular noncompaction MGI:1914797 Mus musculus (house mouse) 67547 Slc39a8 author statement supported by traceable reference
  • PMID:29337306

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025