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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 **6626 - 6650** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0080322	polycystic kidney disease	Atg6 Delta Sod3 oxt	36232 38288 42313 42850	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110665	congenital myasthenic syndrome 3B Aliases: CMS3B congenital myasthenic syndrome 3B, fast-channel	nAChRalpha1 nAChRalpha2 nAChRbeta2	42918 42919 42920	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080693	Noonan syndrome-like disorder with loose anagen hair 2	PPP1CB	5500	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112128	X-linked severe congenital neutropenia Aliases: SCNX XLN	LAS17	854353	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111990	immunodeficiency 30 Aliases: IMD30 MSMD due to complete IL12RB1 deficiency MSMD due to complete interleukin 12 receptor beta 1 deficiency Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency	IL12RB1	3594	Homo sapiens (human)	Alliance of Genome Resources
DOID:10587	Krabbe disease Aliases: Diffuse globoid body sclerosis GLOBOID CELL LEUKOENCEPHALOPATHY Galactosylceramide beta-galactosidase deficiency Krabbe's disease Krabbe's leukodystrophy beta galactocerebrosidase deficiency globoid cell leukodystrophy	galc.L	446948	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:13241	Behcet's disease Aliases: Adamantiades-Behcet disease Behcet syndrome Behet's syndrome triple symptom complex	tgfb1.L	397778	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:3069	malignant astrocytoma Aliases: Astrocytic tumor astrocytoma of Cerebrum astrocytoma of brain astroglioma cerebral astrocytoma	Adgrb1 Akt1 Akt2 Akt3 Atrx Braf Bst2 Cadm2 Camk2g Il16 Kras Map2k3 Nf1 Slc7a5	107831 109880 11651 11652 12325 16170 16653 18015 20539 22589 23797 239857 26397 69550	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:446	primary hyperaldosteronism Aliases: Cushing syndrome Cushing's syndrome hyperaldosteronism	PEP4	855949	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:594	panic disorder Aliases: panic anxiety syndrome	CCKBR HTR1A MANEA MAOA MBL2	3350 4128 4153 79694 887	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090071	hypogonadotropic hypogonadism 11 with or without anosmia	Tacr3	21338	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1485	cystic fibrosis Aliases: CF mucoviscidosis	MNL1 NFT1 STE6 YOR1	853198 853671 853978 856611	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5844	myocardial infarction Aliases: Myocardial infarct heart attack	ace2 ace adra2b cs epoa kdr ngfb pon1 tek vegfaa	100004455 266751 30682 30747 322339 447803 492331 554230 565980 58133	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0110334	osteogenesis imperfecta type 1 Aliases: OI1 osteogenesis imperfecta type I	Col1a1	29393	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:14067	Plasmodium falciparum malaria Aliases: Malaria fever, subtertian falciparum malaria malignant tertian fever	Zw	32974	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0111564	hypoplastic or aplastic tibia with polydactyly Aliases: Werner mesomelic syndrome absence of tibia with polydactyly absent tibia-polydactyly syndrome hypoplastic tibiae-postaxial polydactyly syndrome tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome	SHH	6469	Homo sapiens (human)	Alliance of Genome Resources
DOID:2797	idiopathic interstitial pneumonia Aliases: Diffuse idiopathic pulmonary fibrosis Idiopathic fibrosing alveolitis	Icam1 Mtor	15894 56717	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112318	Schindler disease type 1 Aliases: NAGA deficiency type 1 alpha-N-acetylgalactosaminidase deficiency type 1	Naga	17939	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050951	hereditary ataxia	Cacna1a Cacna1b Pitrm1	12286 12287 69617	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12835	quadriplegia Aliases: tetraplegia	IL6	3569	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050679	blue cone monochromacy	OPN1LW OPN1MW2 OPN1MW3 OPN1MW	101060233 2652 5956 728458	Homo sapiens (human)	Alliance of Genome Resources
DOID:3892	insulinoma Aliases: Insulin-Producing tumor of Islet cells Islet cell adenoma	ins.L ins.S ncam1.L ncam1.S tgfb1.L	378695 378696 397761 397762 397778	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:9643	babesiosis Aliases: Babesiasis Infection by babesia piroplasmosis	Pecam1	29583	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111108	maturity-onset diabetes of the young type 10 Aliases: MODY10	Ins1 Ins2	24505 24506	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080140	multiple congenital anomalies-hypotonia-seizures syndrome 3 Aliases: M syndrome light fixation seizure syndrome	GPI16	856595	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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