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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 **1876 - 1900** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:10534	stomach cancer Aliases: gastric cancer gastric neoplasm	R193.2 W01F3.2 acn-1 acr-2 cest-1.2 daf-1 ddr-2 efn-4 ges-1 gpx-3 gpx-5 grd-2 let-23 lev-1 nkb-1 parp-1 plr-1 ptc-1 ptc-3 sma-6 stim-1 unc-38 unc-63 vab-1 ver-1 ver-4 wrt-6 zmp-4	172105 172150 173631 173794 174044 174274 174462 175182 175201 176575 176829 176882 178269 178633 179914 179991 180349 180351 180622 180638 180780 180936 181178 182256 182513 182726 186632 266823	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060894	early-onset Parkinson's disease Aliases: early-onset Parkinson disease	Psn	40260	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4226	endometrial stromal sarcoma Aliases: ESS Undifferentiated endometrial sarcoma endometrial stromal sarcoma, high grade	kit.L	373579	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:384	Wolff-Parkinson-White syndrome Aliases: Anomalous A-V excitation Wolff-Parkinson-White pattern anomalous atrioventricular excitation	Bmpr1a Map3k7	313121 81507	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112370	Coffin-Siris syndrome 12 Aliases: CSS12	BICRA	29998	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080573	congenital disorder of glycosylation Ix Aliases: congenital disorder of glycosylation 1x	STT3	852862	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10825	essential hypertension Aliases: idiopathic hypertension primary hypertension	asp-1 gcy-28 nep-11 nep-1 nkb-1 nkb-3	172051 173685 174787 180251 181494 182726	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110612	primary ciliary dyskinesia 10 Aliases: CILD10 primary ciliary dyskinesia 10 with or without situs inversus	DNAAF2	55172	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111404	Jalili syndrome Aliases: Cone rod dystrophy-amelogenesis imperfecta syndrome cone-rod dystrophy and amelogenesis imperfecta	cnnm4	100036645	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0090120	hereditary neutrophilia	CSF3R	1441	Homo sapiens (human)	Alliance of Genome Resources
DOID:676	juvenile rheumatoid arthritis Aliases: Pauciarticular onset juvenile chronic arthritis Still's disease acute juvenile rheumatoid arthritis juvenile chronic polyarthritis juvenile idiopathic arthritis monarticular juvenile rheumatoid arthritis pauciarticular juvenile arthritis systemic juvenile rheumatoid arthritis	SMF3	850721	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2893	cervix carcinoma Aliases: cancer of cervix carcinoma cervix uteri carcinoma of cervix carcinoma of the Cervix Uteri	Cd9 Efemp2 Erap1 Ptgs1 Sparc	12527 19224 20692 58859 80898	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9270	alkaptonuria Aliases: Homogentisate 1,2-dioxygenase deficiency alcaptonuria	HGD	3081	Homo sapiens (human)	Alliance of Genome Resources
DOID:12185	otosclerosis	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0090142	cystathioninuria Aliases: cystathionase deficiency cystathione gamma-lyase deficiency syndrome gamma-cystathionase deficiency	Cth	107869	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081022	retinal cone dystrophy 3B Aliases: cone dystrophy with supernormal rod responses	Kcnv2	240595	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081146	common variable immunodeficiency 3	CD19	930	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080567	congenital disorder of glycosylation Ip Aliases: congenital disorder of glycosylation 1p	algn-11	176032	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050445	X-linked dominant hypophosphatemic rickets Aliases: Hypophosphatemia, Vitamin D-Resistant Rickets Vitamin D-Resistant Rickets, X-Linked X-linked hypophosphatemia hypophosphatemic rickets X-linked dominant	famk-1 nep-2	181616 188090	Caenorhabditis elegans	Alliance of Genome Resources
DOID:14250	Down syndrome Aliases: Complete trisomy 21 syndrome Down's syndrome Down's syndrome - trisomy 21 Downs syndrome G Trisomy trisomy 21 syndrome	pofut2	777668	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0080696	Winchester syndrome	MMP14	4323	Homo sapiens (human)	Alliance of Genome Resources
DOID:2626	choroid plexus papilloma Aliases: childhood choroid plexus papilloma	Tp53	24842	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0112189	thyroid dyshormonogenesis 6 Aliases: TDH6 genetic defect in thyroid hormonogenesis 6	DUOX2	50506	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080333	aortic valve disease 1	N	31293	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110734	neurodegeneration with brain iron accumulation Aliases: NBIA	PAN1	854822	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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