GlyCosmos Portal

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

Displaying entries **15026 - 15050** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0070355	overactive bladder syndrome Aliases: OAB overactive bladder urge syndrome urgency-frequency syndrome	BDKRB1 CD40LG NGF NRG1 TRPA1	3084 4803 623 8989 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:891	progressive myoclonus epilepsy Aliases: PME progressive myoclonic epilepsy	Epm2a Scarb2 Sema6b	12492 13853 20359	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13078	eumycotic mycetoma Aliases: Madura foot Maduromycosis, mycotic Mycotic mycetoma eumycetoma maduromycosis	COMT	1312	Homo sapiens (human)	Alliance of Genome Resources
DOID:5744	ovary serous adenocarcinoma Aliases: malignant ovarian serous tumor serous carcinoma of Ovary	zig-11	189580	Caenorhabditis elegans	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:0080523	adult-onset leukoencephalopathy with axonal spheroids and pigmented glia Aliases: hereditary diffuse leukoencephalopathy with spheroids	Csf1r	12978	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4676	uremia Aliases: UREMIA OF renal ORIGIN	Ager Alpl Angpt2 Comt Fgf23 Mstn Th	11596 11601 11647 12846 17700 21823 64654	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111785	frontometaphyseal dysplasia Aliases: FMD	MAP3K7	6885	Homo sapiens (human)	Alliance of Genome Resources
DOID:8677	perinatal necrotizing enterocolitis Aliases: ENTEROCOLITIS NECROTIZING Necrotizing enterocolitis in fetus OR newborn Perinatal necrotising enterocolitis Pseudomembranous enterocolitis in newborn necrotizing enterocolitis	Bnip3 Cd14 Cd40 Cd40lg Egf Hbegf Il10 Il10rb Plaur Ptafr Tjp1 Tlr1 Tlr2 Tlr3 Tlr4 Tlr5 Tlr6 Tlr7 Tlr9 Tnf	12176 12475 13645 142980 15200 16153 16155 170743 18793 19204 21872 21897 21898 21899 21926 21939 21947 24088 53791 81897	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3892	insulinoma Aliases: Insulin-Producing tumor of Islet cells Islet cell adenoma	ADM BTC CUX1 INS NCAM1 SLC2A2 TGFA TGFB1	133 1523 3630 4684 6514 685 7039 7040	Homo sapiens (human)	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:4194	glucose metabolism disease Aliases: disorder of glucose metabolism	daf-2 unc-103	175410 175527	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050579	glycogen storage disease XV Aliases: Glycogen storage disease 15 Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency glycogen storage disease type XV	gyg-1 gyg-2	180119 180644	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2352	hemochromatosis Aliases: Haemochromatosis diabetes bronze iron storage disorder	Hfe Hjv Tfr2 Tnf	15216 21926 50765 69585	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050978	spinocerebellar ataxia type 29	Itpr1	16438	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5434	scrapie	PRNP	5621	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070539	Halperin-Birk syndrome Aliases: HLBKS NEDSOSB NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES	Sec31a Sec31b	240667 69162	Mus musculus (house mouse)	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:0050563	nonsyndromic deafness Aliases: nonsyndromic hearing loss nonsyndromic hereditary hearing loss	DIE2	853142	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070259	congenital disorder of glycosylation type IIg Aliases: CDG IIg CDG2G CDGII/COG1 cerebrocostomandibular-like syndrome CDGIIg Carbohydrate deficient glycoprotein syndrome type IIg	COG1	9382	Homo sapiens (human)	Glyco-Disease Genes Database Alliance of Genome Resources
DOID:0111590	Cohen syndrome Aliases: COH1 Hypotonia, obesity, and prominent incisors Pepper syndrome	VPS13A VPS13B VPS13C	157680 23230 54832	Homo sapiens (human)	Alliance of Genome Resources
DOID:12236	primary biliary cholangitis Aliases: biliary liver cirrhosis cholestatic cirrhosis chronic nonsuppurative destructive cholangitis primary biliary cirrhosis	BPT1 NSP1 PEP4 PHO8 STE6	850645 852092 853409 853671 855949	Saccharomyces cerevisiae S288C	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

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