GlyCosmos Portal

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

Displaying entries **14376 - 14400** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:480	movement disease	Drd2	24318	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1067	open-angle glaucoma Aliases: Wide-angle glaucoma glaucoma simplex open angle glaucoma pigmentary glaucoma	ADRB2 APOC3 APOE GMDS IL10 IL2 MYOC OPTN PON1 TAP1 TNF	10133 154 2762 345 348 3558 3586 4653 5444 6890 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111366	familial hepatic adenoma Aliases: familial liver cell adenomas	HNF1A	6927	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080322	polycystic kidney disease	Atf1 C9 Ctsb Ctsh Dll4 Ganab Gnas Gpbar1 Kif3a Mtor Myc Nos3 Pkd1 Pkd2 Pla2g4a Pparg Ptgs1 Ptgs2 Ptma Sod1 Stam2 Stam Tnc Xylt2	11908 12279 13030 13036 14376 14683 16568 17869 18127 18763 18764 18783 19016 19224 19225 19231 20655 20844 217119 21923 227289 54485 56324 56717	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1496	echinococcosis Aliases: Echinococcosis of liver echinococcal disease hepatic echinococcosis hydatid disease hydatidosis liver echinococcus pulmonary echinococcosis	ABO	28	Homo sapiens (human)	Alliance of Genome Resources
DOID:11963	esophagitis Aliases: acute esophagitis	BMP4 IL4R PTGS2 SLC7A5 TNF	3566 5743 652 7124 8140	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111029	hemochromatosis type 1 Aliases: HFE1 symptomatic form of HFE-related hereditary hemochromatosis symptomatic form of classic hemochromatosis symptomatic form of hemochromatosis type 1	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110645	long QT syndrome 2 Aliases: LQT2	alg10	100331575	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0060786	hypomyelinating leukodystrophy Aliases: HLD	DEGS1 POLR3A POLR3B	11128 55703 8560	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050700	cardiomyopathy Aliases: Cardiomyopathies	ncam1.L ncam1.S pomt1.S	108699937 397761 397762	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0080410	familial adenomatous polyposis 2 Aliases: MUTYH-associated polyposis MUTYH-related attenuated FAP MUTYH-related attenuated familial adenomatous polyposis MUTYH-related attenuated familial polyposis coli	Mutyh	170841	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:865	vasculitis Aliases: Angiitis	Cast Il10 Mpo Nos3 Serpina3a Serpina3b Serpina3c Serpina3f Serpina3j Serpina3k Serpina3m Serpina3n	12380 16153 16625 17523 18127 20714 20716 20717 238393 238395 271047 74069	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080991	congenital myopathy 1B Aliases: multiminicore disease	RYR1	6261	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070219	familial hyperinsulinemic hypoglycemia 1 Aliases: HHF1	YBT1	850678	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1761	Melkersson-Rosenthal syndrome Aliases: Cheilitis granulomatosa of Mescher-Melkersson-Rosenthal Melkersson's syndrome	H2-D1 H2-K1 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7	110557 14964 14972 15006 15007 15013 15015 15018	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080470	developmental and epileptic encephalopathy 36 Aliases: congenital disorder of glycosylation, type Is early infantile epileptic encephalopathy 36	algn-13	179890	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080987	Ehlers-Danlos syndrome periodontal type 2	C1s1 C1s2	317677 50908	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060611	abdominal obesity-metabolic syndrome	DDX17 DDX5 GUCY2C LEP NEIL1 PPARG PPARGC1A SIRT3 SLC2A9	10521 10891 1655 23410 2984 3952 5468 56606 79661	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111773	46,XY sex reversal 8 Aliases: SRXY8 TDD male pseudohermaphroditism due to deficiency of testicular 17,20-desmolase	GCY1 YPR1	851974 854287	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080253	Meckel syndrome 13	tmem107.L	735183	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0050575	D-2-hydroxyglutaric aciduria	IDH1	3417	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070277	primary autosomal recessive microcephaly 15 Aliases: MCPH15 NEDMISBA neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities	Mfsd2a	76574	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1742	drug psychosis Aliases: Drug-induced psychosis Drug-induced psychotic disorder	Drd2 Oprm1	24318 25601	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050534	congenital stationary night blindness Aliases: congenital essential nyctalopia	Cacna1f Gucy2e Nyx Trpm1	14919 17364 236690 54652	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060439	lysinuric protein intolerance Aliases: LPI dibasic amino aciduria II hyperdibasic aminoaciduria	Slc7a7	83509	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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