GlyCosmos Portal

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

Displaying entries **3726 - 3750** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:1686	glaucoma	Ance-3 Atg6 Jra	34808 36057 42850	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:8986	narcolepsy Aliases: Narcolepsy, without cataplexy paroxysmal sleep	Cd40lg Hcrtr2	25605 84349	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111333	early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome Aliases: EMARDD Myopathy, areflexia, respiratory distress, and dysphagia, early-onset congenital myopathy 10A	MEGF10	84466	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060604	ankyloglossia Aliases: tongue-tie	Lgr5	299802	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050625	biliary tract benign neoplasm Aliases: extrahepatic bile duct neoplasm neoplasm of extrahepatic bile ducts tumor of the extrahepatic bile duct	CG31115 Mtap	318597 36955	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070272	hereditary nonpolyposis colorectal cancer type 5 Aliases: HNPCC5	MSH6	2956	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111883	Diamond-Blackfan anemia 5 Aliases: DBA5 RPL35A-related Diamond-Blackfan anemia	RPL35A	6165	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060776	congenital diarrhea 5 with tufting enteropathy Aliases: DIAR5 congenital diarrhoea 5 with tufting enteropathy congenital familial intractable diarrhea with epithelial or epithelium abnormalities congenital familial intractable diarrhoea with epithelial or epithelium abnormalities congenital tufting enteropathy tufting enteropathy	EPCAM	4072	Homo sapiens (human)	Alliance of Genome Resources
DOID:3307	teratoma	Pgm1	44010	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060901	lymphoplasmacytic lymphoma Aliases: Waldenstroem's macroglobulinemia Waldenstrom Macroglobulinemia lymphoplasmacytic lymphoma with IgM gammopathy	gpx-3 gpx-5	181178 182513	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050866	oral squamous cell carcinoma Aliases: mouth squamous cell carcinoma	ABL1 AGAP2 ARID2 ARPC1B ATM AZGP1 BIRC2 BRINP2 BST2 CALR CBX2 CCL2 CCR2 CDC73 CDH1 CHAF1B CLPTM1L CTNND1 CYP1A1 CYP24A1 CYP2E1 DAXX DDR1 DDR2 DOCK6 EGFR ERBB2 ERBB4 EZH2 FAT1 FGFR3 FGFR4 FLT3 FOSL2 GAPDH GSK3B H2AX HP IL10 IL13RA2 IL2 IL6 JUN JUNB KMT2D MET PLAU PLCG1 PRDX2 PTEN PTGIS PTPN13 RELA SERPINE1 SKP2 SLC7A5 TERT TET2 TNF TP53 TTR WNT11	10095 116986 1500 1543 1571 1591 1616 1956 196528 2064 2066 2146 2195 2261 2264 2322 2355 25 2597 2932 3014 3240 329 3558 3569 3586 3598 3725 3726 4233 472 4921 5054 5328 5335 54790 563 5728 5740 57572 57795 5783 5970 6347 6502 684 7001 7015 7124 7157 7276 729230 7481 780 79577 8085 81037 811 8140 8208 84733 999	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081242	autoimmune interstitial lung, joint, and kidney disease Aliases: Autoimmune interstitial lung disease-arthritis syndrome COPA syndrome	Copa	12847	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111666	proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Aliases: EPV Fowler syndrome Fowler vasculopathy PVHH cerebral proliferative glomeruloid vasculopathy encephaloclastic proliferative vasculopathy hydranencephaly, Fowler type hydrocephaly/hydranencephaly due to cerebral vasculopathy proliferative vasculopathy and hydranencephaly/hydrocephaly	Slc7a2 Slc7a3	11988 11989	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050567	orofacial cleft	Axn	43565	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080520	Tn polyagglutination syndrome Aliases: galactosyltransferase deficiency	C1galt1c1	302499	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080676	Stickler syndrome 1	col2a1	394828	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0110669	congenital myasthenic syndrome 14 Aliases: CMS14 CMSTA3 congenital myasthenic syndrome 14, with tubular aggregates congenital myasthenic syndrome with tubular aggregates 3	Alg2	56737	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2349	arteriosclerosis Aliases: Arteriosclerotic vascular disease	Fur1 Idgf1 Idgf2 Idgf3 Idgf4 Idgf5 Idgf6 Snmp2 Spn28Dc Tl mew scb	31926 32275 34091 34978 34979 34981 36692 36868 37104 38868 43222 47220	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:687	hepatoblastoma	cdh1.S	100337618	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0080114	mitochondrial complex III deficiency nuclear type 5	Uqcrc2	67003	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5015	fibrolamellar carcinoma Aliases: Fibrolamellar hepatocellular carcinoma Hepatocellular carcinoma, fibrolamellar Oncocytic Hepatocellular tumor	CA12 CTNNB1 FGFR1	1499 2260 771	Homo sapiens (human)	Alliance of Genome Resources
DOID:3907	lung squamous cell carcinoma Aliases: Epidermoid cell carcinoma of the lung	clptm1l csf1ra fgfr4	100000160 436653 64274	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0060864	patterned macular dystrophy 2 Aliases: MDPT2 butterfly-shaped pigmentary maculary dystrophy 2	CTNNA1	1495	Homo sapiens (human)	Alliance of Genome Resources
DOID:3635	congenital myasthenic syndrome	Chrna1 Chrna2 Chrna4 Chrna6 Chrne Syt1 Syt2	170945 24805 25590 25716 29422 79557 81721	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:5409	lung small cell carcinoma	Acvr1b Apoc3 Atrx Chrna3 Chrna5 Chrnb4 Csf1r Dll4 Eef2 Fat1 Itgb1 Kdm6a Lama3 Lamb3 Lamc2 Max Mtor Notch1 Pik3r1	108015 110834 110835 11479 11814 12978 13629 14107 16412 16774 16780 16782 17187 18128 18708 22289 22589 54485 56717	Mus musculus (house mouse)	Alliance of Genome Resources

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