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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 **15051 - 15075** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0111555	Alkuraya-Kucinskas syndrome Aliases: ALKKUCS	CSF1	850776	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0110290	autosomal recessive limb-girdle muscular dystrophy type 2X Aliases: LGMD2X muscular dystrophy, limb-girdle, type 2X	Bves	23828	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081223	glycosylphosphatidylinositol biosynthesis defect 16 Aliases: Intellectual developmental disorder, autosomal recessive 62	PIGC	5279	Homo sapiens (human)	Alliance of Genome Resources
DOID:3114	serous cystadenocarcinoma Aliases: serous adenocarcinoma serous carcinoma	Lhcgr Trp53	16867 22059	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111533	gnathodiaphyseal dysplasia Aliases: GDD Levin syndrome 2 gnathodiaphyseal sclerosis osteogenesis imperfecta with unusual skeletal lesions osteogenesis imperfecta, Levin type	Ano5	233246	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12960	acrocephalosyndactylia Aliases: Apert syndrome	Fgfr1 Fgfr2	14182 14183	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050742	nicotine dependence Aliases: tobacco use disorder	comta comtb	561372 565370	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:11612	polycystic ovary syndrome Aliases: Multicystic ovaries PCOS Polycystic Ovarian disease Polycystic ovaries Stein-Leventhal synd. Stein-Leventhal syndrome polycystic ovary	comta comtb fsta vegfaa	100004116 30682 561372 565370	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0110773	hereditary spastic paraplegia 2 Aliases: SPG2 X-linked spastic paraplegia 2 spastic paraplegia type 2	PLP1	5354	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090117	thiamine-responsive megaloblastic anemia syndrome Aliases: Rogers syndrome THMD1 TRMA thiamine metabolism dysfunction syndrome 1 thiamine-responsive anaemia syndrome thiamine-responsive anemia syndrome thiamine-responsive megaloblastic anaemia syndrome thiamine-responsive megaloblastic anaemia with diabetes mellitus and sensorineural deafness thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness thiamine-responsive myelodysplasia	Slc19a2	116914	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10941	intracranial aneurysm Aliases: brain aneurysm	Aoc3 Ccl2 Col1a2 Cst3 Ctsk Ctss Mmp2 Mmp9 Nos3 Timp1 Tnf Vcan Vegfa	114122 116510 24600 24770 24835 25307 29175 29473 50654 81686 81687 83785 84352	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1324	lung cancer	Acer Ance Axn Calr Egfr Hs3st-B Pxn Stim nAChRalpha1 nAChRalpha2 nAChRalpha6 nAChRbeta1 nAChRbeta2	32556 32918 34189 34304 34805 37455 38326 38545 41166 42918 42919 42920 43565	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4467	clear cell renal cell carcinoma Aliases: Clear cell carcinoma of kidney clear cell kidney carcinoma conventional (Clear cell) renal cell carcinoma conventional renal cell carcinoma renal clear cell carcinoma	ACKR3 AGER BAX CXCR4 DDR1 ENG EP300 F2 FTO GATA2 IGF1R KAT8 MMP12 MYC PAK4 PDGFB SETD2 SMARCB1 SRSF4 SRSF5 SRSF6 SRSF7 TP53	10298 177 2022 2033 2147 2624 29072 3480 4321 4609 5155 57007 581 6429 6430 6431 6432 6598 7157 780 7852 79068 84148	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2 Aliases: CVPT2	CASQ2	845	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111635	autosomal recessive nonsyndromic deafness 57 Aliases: DFNB57 autosomal recessive deafness 57	PDZD7	79955	Homo sapiens (human)	Alliance of Genome Resources
DOID:12556	acute kidney tubular necrosis Aliases: ATN - acute tubular necrosis acute renal Failure with tubular necrosis acute renal failure with lesion of tubular necrosis acute tubular necrosis acute tubule necrosis	GLR1	856014	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111639	autosomal recessive nonsyndromic deafness 109 Aliases: DFNB109 autosomal recessive deafness 109	fus	44095	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:10155	intestinal cancer Aliases: malignant intestinal tumors malignant neoplasm of intestine	Egfr Emc1 Erbb2 Erbb3 Erbb4 Kras Lyn Mpc2 Notch1 Notch2 Notch3 Ptpn2 Sox2 Src Wwtr1 Yap1 Yes1	13649 13866 13867 13869 16653 17096 18128 18129 18131 19255 20674 20779 22601 22612 230866 70456 97064	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050827	rheumatic heart disease Aliases: rheumatic carditis	W01F3.2 gpd-1 gpd-3 gpd-4 scav-2 scav-3 zmp-4	174578 174603 176673 176787 179991 180351 180601	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0070149	hereditary sensory and autonomic neuropathy type 7 Aliases: HSAN7 hereditary sensory and autonomic neuropathy type VII	Scn11a	29701	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9253	gastrointestinal stromal tumor Aliases: GANT GIST Stromal tumor of gastrointestinal tract Stromal tumour of gastrointestinal tract gastrointestinal stromal tumour	csf1ra kita	30256 64274	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:1495	cystic echinococcosis Aliases: Echinococcus granulosus infection Echinococcus granulosus infection of lung Echinococcus granulosus infection of thyroid Liver echinococcus granulosus Thyroid echinococcus granulosus echinococcus granulosus echinococcus granulosus infectious disease echinococcus granulosus infectious disease of liver echinococcus granulosus infectious disease of thyroid lung echinococcus granulosus unilocular echinococcosis unilocular hydatid disease	H2-Ab1 H2-Eb1 Il4 Tlr2 Tlr4	14961 14969 16189 21898 24088	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111373	familial progressive hyperpigmentation with or without hypopigmentation Aliases: FPHH MUH melanosis universalis hereditaria	Kitlg	60427	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0081317	multiple synostoses syndrome 1	Nog	25495	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110265	cataract 31 multiple types Aliases: CTRCT31	CHMP4B	128866	Homo sapiens (human)	Alliance of Genome Resources

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