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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **8251 - 8275** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:10303	sialadenitis Aliases: Sialoadenitis	Cd4	24932	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:813	septic arthritis Aliases: infectious arthritis	Cd4	24932	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:4231	histiocytoma	Klrk1	24934	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:893	Wilson disease Aliases: Cerebral pseudosclerosis Westphal pseudosclerosis Westphal-Strumpell syndrome Wilson's disease hepatolenticular degeneration	Atp7a Hmgcr	24941 25675	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3144	cutis laxa Aliases: loose skin	Atp7a Fbln5 Ltbp1	24941 29158 59107	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:12377	spinal muscular atrophy	Atp7a Dpp6 Hexb	24941 29272 294673	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111272	occipital horn syndrome Aliases: EDS IX Ehlers-Danlos syndrome type 9 Ehlers-Danlos syndrome type IX X-linked cutis laxa	Atp7a	24941	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1838	Menkes disease Aliases: COPPER TRANSPORT DISEASE Menkes kinky-hair syndrome steely hair syndrome	Atp7a	24941	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111196	X-linked distal spinal muscular atrophy 3 Aliases: ATP7A-related distal motor neuropathy DSMAX SMAX3 X-linked dHMN3 X-linked dSMA3 X-linked distal hereditary motor neuropathy type 3 X-linked recessive distal spinal muscular atrophy	Atp7a	24941	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:896	metal metabolism disorder Aliases: inborn metal metabolism disorder	Atp7a	24941	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050437	Danon disease Aliases: ANTOPOL DISEASE PSEUDOGLYCOGENOSIS II	Lamp2	24944	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:12259	hemophilia B Aliases: Congenital factor IX deficiency Congenital factor IX disorder deficiency, functional factor IX factor IX deficiency	F9	24946	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080839	X-linked warfarin sensitivity	F9	24946	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111899	X-linked thrombophilia due to factor IX defect Aliases: THPH8	F9	24946	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112029	non-syndromic X-linked intellectual disability 50 Aliases: MRX50 X-linked intellectual developmental disorder 50 X-linked mental retardation 50 XLID50	Syn1	24949	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112122	X-linked epilepsy with variable learning disabilities and behavior disorders Aliases: X-linked epilepsy-learning disabilities-behavior disorders syndrome	Syn1	24949	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111031	hemochromatosis type 5 Aliases: FTH1-associated iron overload FTH1-related iron overload HFE5	FTH1	2495	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112306	Mahvash Disease Aliases: GCGR-related hyperglucagonemia nesidioblastosis, alpha cell hyperplasia, microglucagonoma, and nonfunctioning islet cell tumor	Gcgr	24953	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080108	myoglobinuria	Pgam2	24959	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:14723	beta-ketothiolase deficiency Aliases: 2-methyl-3-hydroxybutyricacidemia 3-ketothiolase deficiency 3-oxothiolase deficiency Mitochondrial acetoacetyl-CoA Thiolase deficiency alpha-methylacetoaceticaciduria peroxisomal thiolase deficiency	Acat1	25014	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060832	Griscelli syndrome type 1 Aliases: GS1 Griscelli syndrome with neurological impairment Griscelli syndrome, cutaneous and neurological type Griscelli-Prunieras syndrome type 1 hypopigmentation-neurologic impairment syndrome	Myo5a	25017	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080001	bone disease	Fgfr1 Fgfr2 Fgfr4 Npr3 Pon1	25022 25114 25339 79114 84024	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10486	intestinal atresia	Acta1 Actb Actc1 Fgf10 Fgfr2	25022 25443 29275 29437 81822	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050331	lacrimoauriculodentodigital syndrome 1 Aliases: LEVY-HOLLISTER SYNDROME Lacrimo-auriculo-dento-digital syndrome 1	Fgf10 Fgfr2	25022 25443	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2340	craniosynostosis Aliases: Premature closure of cranial sutures	Fgfr2 Nell1 Nog	25022 25495 81733	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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