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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 **3276 - 3300** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:2986	IgA glomerulonephritis Aliases: Berger's IgA or IgG nephropathy Focal Glomerulonephritis IgA nephropathy primary IgA nephropathy segmental glomerulonephritis	ACE ACSM3 ADD1 ADD2 AGTR1 AGTR2 B4GALT1 C3 CCL2 CCR6 CD14 CFB CHGA CXCR2 FAS FCAR FCGR3A FN1 HAVCR1 HLA-DQB1 IGF1R IL1A IL1RN LCN2 MMP14 MTR MUC20 NGF PDE5A PLA2G7 SELE SELL SERPINB7 SHH SPRY2 STAT4 TLR1 TLR9 TNF TNFRSF1A TNFRSF1B TNFSF13B TNFSF14	10253 10673 1113 118 119 1235 1636 185 186 200958 2204 2214 2335 26762 2683 3119 3480 355 3552 3557 3579 3934 4323 4548 4803 54106 629 6296 6347 6401 6402 6469 6775 7096 7124 7132 7133 718 7941 8654 8710 8740 929	Homo sapiens (human)	Alliance of Genome Resources
DOID:6595	gastric tubular adenocarcinoma Aliases: tubular adenocarcinoma of stomach	Smo	319757	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2349	arteriosclerosis Aliases: Arteriosclerotic vascular disease	pon2	448598	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0080611	anterior segment dysgenesis 6	CYP1B1	1545	Homo sapiens (human)	Alliance of Genome Resources
DOID:1394	urinary schistosomiasis Aliases: Schistosoma Hematobium Infection Schistosoma haematobium Schistosoma hematobium infectious disease Schistosomiasis due to schistosoma haematobium Schistosomiasis of bladder Vesical schistosomiasis bladder Schistosomiasis cystitis with bilharziasis	CD1D CTLA4 IL5 STAT6	1493 3567 6778 912	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050809	mucopolysaccharidosis IX	Hyal1	367166	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:4797	SM-AHNMD Aliases: systemic mastocytosis with associated clonal haematological non-mast cell lineage disease systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease	ASXL1	171023	Homo sapiens (human)	Alliance of Genome Resources
DOID:12287	Crimean-Congo hemorrhagic fever Aliases: CHF Congo virus Congo-Crimean Hemorrhagic Fever Crimean hemorrhagic fever	Ifna11 Ifna12 Ifna13 Ifna16 Ifna1 Ifna4 Ifna9	15962 15964 15967 15972 230396 230398 242519	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10873	Kuhnt-Junius degeneration Aliases: Exudative senile macular degeneration of retina Neovascular age-related macular degeneration Senile macular degeneration, wet Wet senile macular retinal degeneration	InR tor	35717 42549	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110870	congenital stationary night blindness 1A Aliases: CSNB1A NBMI complete CSNB X-linked congenital stationary night blindness 1A X-linked congenital stationary night blindness with myopia hemeralopia-myopia myopia-night blindness	Nyx	236690	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112026	non-syndromic X-linked intellectual disability 99 Aliases: MRX99 X-linked mental retardation 99	faf	43749	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:12577	urethral obstruction Aliases: Obstruction of urethra	Gja1 Tgfb1	14609 21803	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050717	methylmalonic aciduria and homocystinuria type cblF Aliases: Cobalamin F deficiency MAHCF	Lmbrd1	246046	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070332	multiple mitochondrial dysfunctions syndrome 6	PMPCB UQCRC1	7384 9512	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070347	encephalopathy due to defective mitochondrial and peroxisomal fission 1	Dnm1l	114114	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111725	geleophysic dysplasia 1 Aliases: GPHYSD1	ADAMTSL2	9719	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111444	progressive myoclonus epilepsy 4 Aliases: AMRF EPM4 Myoclonus-nephropathy syndrome action myoclonus-renal failure syndrome	SCARB2	950	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110229	cataract 6 multiple types Aliases: CTRCT6	vab-1	173794	Caenorhabditis elegans	Alliance of Genome Resources
DOID:479	angiokeratoma Aliases: Angiokeratoma of skin Cutaneous Angiokeratoma skin angiokeratoma	NAGA	4668	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080197	congenital muscular dystrophy with cataracts and intellectual disability	INPP5K	51763	Homo sapiens (human)	Alliance of Genome Resources
DOID:7596	asbestos-related lung carcinoma	Adam28	13522	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8354	complement component 3 deficiency Aliases: C3 deficiency	C3	24232	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:10632	Wolfram syndrome Aliases: WFS	WFS1	7466	Homo sapiens (human)	Alliance of Genome Resources
DOID:12270	coloboma Aliases: coloboma of eye coloboma of macula congenital ocular coloboma	fz2 ptc	35851 40090	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110545	autosomal dominant nonsyndromic deafness 13 Aliases: DFNA13 autosomal dominant deafness 13	COL11A2	1302	Homo sapiens (human)	Alliance of Genome Resources

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