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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 **3801 - 3825** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0080281	schizophrenia 19	RBM12	10137	Homo sapiens (human)	Alliance of Genome Resources
DOID:11105	fundus albipunctatus Aliases: Pigmentary retinal dystrophy retinitis punctata albescens	prph2.S rho.L rho.S	108715858 380209 398002	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0111167	Dyggve-Melchior-Clausen disease Aliases: DMC disease pseudo-Morquio disease type I	Rab8b	235442	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:987	alopecia	Bdnf Dsg4 Esr2 H2-D1 H2-K1 H2-M2 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7 H2-T3 Prss8	110557 12064 13983 14964 14972 14990 15006 15007 15013 15015 15018 15043 16769 76560	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070537	spastic tetraplegia, thin corpus callosum, and progressive microcephaly Aliases: SPATCCM	SLC1A4	6509	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080751	keratosis pilaris atrophicans	LRP1	4035	Homo sapiens (human)	Alliance of Genome Resources
DOID:769	neuroblastoma	asic-2 daf-2 mec-10 mec-4 scd-2	175410 179054 181101 181728 189058	Caenorhabditis elegans	Alliance of Genome Resources
DOID:12177	common variable immunodeficiency Aliases: CVID acquired agammaglobulinemia acquired hypogammaglobulinemia common variable agammaglobulinemia sporadic hypogammaglobulinemia	Fcgr2a Fcgr2al1 Fcgr2b Icos Pecam1	116591 289211 29583 498276 64545	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:1062	Fanconi syndrome Aliases: Congenital Fanconi syndrome De Toni-Fanconi syndrome Fanconi-de Toni syndrome Fanconi-de-Toni syndrome Infantile nephropathic cystinosis Lignac-Fanconi syndrome adult Fanconi Anemia adult Fanconi syndrome deToni Fanconi syndrome	ERS1	850438	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080060	autosomal recessive spinocerebellar ataxia 12 Aliases: SCAR12	ENV9	854420	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060462	Desbuquois dysplasia Aliases: Desbuquois syndrome micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification	xylt1	560951	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0050680	Boomerang dysplasia	Flnb	286940	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1742	drug psychosis Aliases: Drug-induced psychosis Drug-induced psychotic disorder	Dop2R	33007	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110791	hereditary spastic paraplegia 3A Aliases: FSP1 SPG3A autosomal dominant familial spastic paraplegia 1 autosomal dominant spastic paraplegia 3 autosomal dominant spastic paraplegia type 3 strumpell disease	Atl3	109168	Mus musculus (house mouse)	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	YPR1	851974	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0112365	spondylocostal dysostosis 1 Aliases: SCDO1 autosomal recessive spondylocostal dysostosis 1	dlb dlc	30120 30141	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:3393	coronary artery disease Aliases: CHD Coronary disease coronary arteriosclerosis coronary heart disease	BPT1 BUD2 CTS2 EMI2 GLK1 GLR1 HMG1 HMG2 HXK1 HXK2 OGG1 VVS1	850317 850614 850645 851171 851977 852128 852543 852639 853770 854900 854942 856014	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:8991	cervix uteri carcinoma in situ Aliases: CIN III CIN III - carcinoma in situ of cervix CIN III - severe dyskaryosis Cervix Ca in situ Severe Dysplasia of the Cervix Uteri Severe dysplasia of cervix carcinoma in situ of cervix carcinoma in situ of uterine cervix carcinoma of cervix stage 0 cervical intraepithelial neoplasia grade III with severe dysplasia squamous intraepithelial neoplasia, grade III	Cadm1 Cd46 Cdh1 Cdkn1b Faslg Igfbp3 Mmp2 Phb1 Ptgs2 Vegfa	24484 25344 25385 29333 29527 363058 81686 83502 83571 83785	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9597	Krukenberg carcinoma Aliases: Krukenberg neoplasm	Cd44	12505	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080860	primary ovarian insufficiency 3	FOXL2	668	Homo sapiens (human)	Alliance of Genome Resources
DOID:12388	neurohypophyseal diabetes insipidus Aliases: Pituitary diabetes insipidus Vasopressin deficiency vasopressin defective diabetes insipidus	Avp	11998	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060448	Fleck corneal dystrophy Aliases: FCD Francois-Neetens speckled corneal dystrophy	FAB1	850574	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070250	autosomal dominant Emery-Dreifuss muscular dystrophy 5 Aliases: EDMD5 Emery-Dreifuss muscular dystrophy 5, autosomal dominant	Syne2	319565	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3907	lung squamous cell carcinoma Aliases: Epidermoid cell carcinoma of the lung	Atrx Bsg Chrna5 Chrnb4 Clptm1l Csf1r Ctnnb1 Ddr2 Fap Fgf9 Fgfr4 Frzb Gpx1 Idh1 Idh2 Lamc2 Ptch1 Ptpn13 Ptprj Sftpb Slc7a5 Src	108015 110835 12215 12387 12978 14089 14180 14186 14775 15926 16782 18214 19206 19249 19271 20378 20388 20539 20779 218335 22589 269951	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3390	palmoplantar keratosis Aliases: Keratosis palmaris et plantaris Palmoplantar Keratoderma palmo-plantar keratodermas	Gja1 Jup	14609 16480	Mus musculus (house mouse)	Alliance of Genome Resources

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