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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 **13976 - 14000** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▲	Source
DOID:0070413	autosomal recessive spinocerebellar ataxia 32 Aliases: SCAR32	Prdx3	64371	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111815	low molecular weight proteinuria with hypercalciuric nephrocalcinosis	Clcn3	84360	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:479	angiokeratoma Aliases: Angiokeratoma of skin Cutaneous Angiokeratoma skin angiokeratoma	Naga	315165	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080557	congenital disorder of glycosylation Ie Aliases: congenital disorder of glycosylation 1e	Dpm1	296394	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070254	congenital disorder of glycosylation type IIb Aliases: CDG IIb CDG2B CDGIIb glucosidase I deficiency	Mogs	78947	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9007	sudden infant death syndrome Aliases: Cot death Crib death SIDS Sudden death of nonspecific cause in infancy	Scn5a Slc6a4 Vegfa	25553 25665 83785	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:0110157	Charcot-Marie-Tooth disease type 2J Aliases: CMT2J Charcot-Marie-Tooth disease type 2 with hearing loss and pupillary abnormalities Charcot-Marie-Tooth neuropathy type 2J	Mpz	24564	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:627	severe combined immunodeficiency Aliases: SCID combined T and B cell inborn immunodeficiency	Cd3d Il2 Ptprc	116562 24699 25710	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0060700	familial hypocalciuric hypercalcemia 1 Aliases: FHH type 1 HHC1 familial benign hypercalcemia 1 familial hypocalciuric hypercalcemia type I hypocalciuric hypercalcemia type I	Casr	24247	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3798	pleural empyema Aliases: Empyema of pleura Empyema of pleura without fistula Empyema with no fistula Empyema with pleural fistula Empyema without mention of fistula Empyema, chest Pleural empyema with fistula Purulent pleurisy Thorax abscess abscess of pleural cavity abscess of thorax empyema empyema with fistula lung empyema pleural empyema with no fistula purulent pleuritis pyothorax	Tnc	116640	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:331	central nervous system disease	Aco2 Gria1 Gria2 Gria3 Gria4 Hgf	24446 29627 29628 29629 50592 79250	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2384	Wernicke encephalopathy Aliases: Wernicke's disease Wernicke's encephalopathy	Ptgs2	29527	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:5022	aflatoxins-related hepatocellular carcinoma	Ggt1	116568	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9253	gastrointestinal stromal tumor Aliases: GANT GIST Stromal tumor of gastrointestinal tract Stromal tumour of gastrointestinal tract gastrointestinal stromal tumour	Sdha Sdhb Shh Slco1b2 Stim1	157074 29499 298596 361618 58978	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1068	juvenile glaucoma Aliases: Glaucoma of childhood	Myoc	81523	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1679	cystitis	Adcyap1r1 Bdnf Cx3cl1 Esr2 Il2 Il4 Kdr Lta Ngf Ngfr Ptger4 Ptgs2 Sod2 Tacr1 Tnf	116562 24167 24225 24596 24787 24807 24835 25008 25149 25589 287287 29527 310738 84023 89808	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10772	thrombotic thrombocytopenic purpura Aliases: Moschcowitz's syndrome	Proc Tfpi	25268 29436	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:12554	hemolytic-uremic syndrome Aliases: haemolytic-uraemic syndrome hemolytic uremic syndrome	C1galt1c1 Ccl2 Cd46 Hp Il1rl1 Il1rn Plat	24464 24770 25556 25692 29333 302499 60582	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080762	autosomal recessive limb-girdle muscular dystrophy type 2Z Aliases: limb-girdle muscular dystrophy 21	Poglut1	288091	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:423	myopathy	Actb Clcnkb Hmgcr Lmnb1 Pdlim5 Pdlim7	116685 25675 286908 64353 79430 81822	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112310	central precocious puberty 1 Aliases: CPPB1	Kiss1r	78976	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10941	intracranial aneurysm Aliases: brain aneurysm	Aoc3 Ccl2 Col1a2 Cst3 Ctsk Ctss Mmp2 Mmp9 Nos3 Timp1 Tnf Vcan Vegfa	114122 116510 24600 24770 24835 25307 29175 29473 50654 81686 81687 83785 84352	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070149	hereditary sensory and autonomic neuropathy type 7 Aliases: HSAN7 hereditary sensory and autonomic neuropathy type VII	Scn11a	29701	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111373	familial progressive hyperpigmentation with or without hypopigmentation Aliases: FPHH MUH melanosis universalis hereditaria	Kitlg	60427	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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