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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 **2501 - 2525** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:14400	capillary leak syndrome	pon2	448598	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0112234	microlissencephaly	Tuba1a Tuba1b Tuba1c Tuba3a Tuba3b Tuba4a Tuba8	22142 22143 22144 22145 22146 22147 53857	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2986	IgA glomerulonephritis Aliases: Berger's IgA or IgG nephropathy Focal Glomerulonephritis IgA nephropathy primary IgA nephropathy segmental glomerulonephritis	Acer Ance InR beta4GalNAcTA	34189 34805 36585 42549	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:14784	olivopontocerebellar atrophy Aliases: Dejerine-Thomas syndrome Thomas' syndrome WADIA-SWAMI SYNDROME	APTX	54840	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080081	nonsyndromic congenital nail disorder 3	plcd1.L plcd1.S	108718712 108719811	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0111579	asthma, nasal polyps, and aspirin intolerance Aliases: ASA triad	Ptger2	81752	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0090100	ocular albinism with sensorineural deafness Aliases: WS2-OA autosomal recessive Waardenburg syndrome type 2 with ocular albinism digenic Waardenburg syndrome/albinism digenic Waardenburg syndrome/ocular albinism	MITF	4286	Homo sapiens (human)	Alliance of Genome Resources
DOID:2526	prostate adenocarcinoma	Akt1 Akt2 Akt3 Cd9 Clu Creb3l4 Igf1r Kdr Myc Pam Pdgfa Pdgfra	24185 24577 24854 24936 25233 25266 25267 25508 25589 25718 29414 310616	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080954	arthrogryposis multiplex congenita	Syne1	64009	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060227	Adams-Oliver syndrome Aliases: Adams Oliver syndrome	H12D21.10 glp-1 spe-9	173042 176286 179990	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111035	CADASIL 1 Aliases: autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1	N	31293	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:1206	Rett syndrome Aliases: Rett's disorder cerebroatrophic hyperammonemia	Mecp2	29386	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:3343	glycoproteinosis Aliases: Mucolipidosis type I sialidosis	GNPTAB GNPTG MCOLN1 MCOLN3 NEU1	4758 55283 57192 79158 84572	Homo sapiens (human)	Glyco-Disease Genes Database Glyco-Disease Genes Database Glyco-Disease Genes Database Glyco-Disease Genes Database Glyco-Disease Genes Database Glyco-Disease Genes Database Glyco-Disease Genes Database Glyco-Disease Genes Database Alliance of Genome Resources
DOID:0050830	peripheral artery disease	BUD2	853770	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9261	nasopharynx carcinoma Aliases: Nasopharyngeal carcinoma malignant Nasopharyngeal tumor malignant neoplasm of nasopharynx nasopharynx cancer	ARID1A ATM ATR BRCA1 CALR CD163 CHRNA5 CLPTM1L CR2 CSF1R CXCR4 CYP2E1 DDR2 EFNB2 ERBB3 EZH2 FGFR4 FLT1 FOSL2 FUBP1 GPX1 GRIN2A KDM3A KDR KMT2C MAP2K4 MAPK14 MST1R MUC5B PPIA RAC1 SNRPD1 SNRPE SPEN SRC STAT3 TERT TET2 TNFAIP3 TP53 VEGFA XRCC1	1138 1380 1432 1436 1571 1948 2065 2146 2264 23013 2321 2355 2876 2903 3791 4486 472 4921 545 5478 54790 55818 58508 5879 6416 6632 6635 6714 672 6774 7015 7128 7157 727897 7422 7515 7852 81037 811 8289 8880 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:11077	brucellosis Aliases: Maltese fever undulant fever	CD163 IFNG	3458 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111926	spermatogenic failure 39 Aliases: SPGF39	DNAH17	8632	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070229	intrahepatic cholestasis of pregnancy 3 Aliases: ICP3 pregnancy related cholestasis 3	Mdr49 Mdr65	36428 38726	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:231	motor neuron disease	Dctn1 Kif5b Sod1 Vapa Vwa1	13191 16573 20655 246228 30960	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:446	primary hyperaldosteronism Aliases: Cushing syndrome Cushing's syndrome hyperaldosteronism	asp-1 clh-1 dop-2 srp-6 srp-7	174821 179125 179195 179347 180251	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070058	Helsmoortel-Van Der Aa Syndrome Aliases: HVDAS MRD28 autosomal dominant mental retardation 28	ADNP	23394	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111074	progressive familial heart block type IA Aliases: PFHB1A	Scn5a	20271	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111526	Mullerian aplasia and hyperandrogenism Aliases: Mullerian duct failure and hyperandrogenism WNT4 deficiency	wnt4.L	397706	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:13550	angle-closure glaucoma Aliases: ACG - Angle-closure glaucoma Angle Closure Glaucoma Closed angle glaucoma Narrow cleft glaucoma primary open-angle glaucoma with narrow angles	Hgf Mmp9 Nos3	24446 24600 81687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080158	herpes simplex virus keratitis Aliases: dendritic keratitis	Tl	43222	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources

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