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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 **15851 - 15875** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:2297	leptospirosis Aliases: Fort Bragg fever Leptospirosis icterohaemorrhagica Rat Catcher's Yellows Weil's disease nanukayami fever spirochetal jaundice	ache	114549	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0081355	congenital myopathy 22B	para	32619	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050963	spinocerebellar ataxia type 13	Kcnc3	16504	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112315	brain small vessel disease 3 Aliases: BSVD3	Colgalt1	290637	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050816	urofacial syndrome Aliases: Ochoa syndrome hydronephrosis with peculiar facial expression	sma-10	176849	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050683	Bothnia retinal dystrophy Aliases: Vasterbotten dystrophy	RLBP1	6017	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112231	lissencephaly 7 with cerebellar hypoplasia Aliases: LIS7	CDK5	1020	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060180	colitis	Adipoq Adrb3 Arrb1 Bmp6 Cckbr Ccl2 Cd40 Crhr2 Cxcr2 Esr2 H2-D1 H2-K1 H2-M2 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7 H2-T3 Havcr1 Hp Icam1 Icos Ikbkb Il10 Il17a Kdr Nos3 Ntrk1 Ntrk2 Ppargc1a Ptgs2 Rela Sell Selp Sis Tacr1 Tacr2 Tlr3 Tlr4 Vcam1	109689 110557 11450 11556 12161 12426 12765 12922 13983 142980 14964 14972 14990 15006 15007 15013 15015 15018 15043 15439 15894 16150 16153 16171 16542 171283 18127 18211 18212 19017 19225 19697 20296 20343 20344 21336 21337 21898 21939 22329 54167 69983	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4441	dysgerminoma	ver-4	186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9268	glycine encephalopathy Aliases: Non-ketotic hyperglycinemia nonketotic hyperglycinemia	AMT GCSH GLDC SLC6A9	2653 2731 275 6536	Homo sapiens (human)	Alliance of Genome Resources
DOID:61	mitral valve disease Aliases: Mitral RH valve dis. Rheumatic mitral insufficiency Rheumatic mitral valve changes Rheumatic mitral valve regurgitation chronic rheumatic mitral valve disease of mitral valve rheumatic disease of mitral valve rheumatic mitral valve incompetence	Ace	11421	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13375	temporal arteritis Aliases: Horton's disease giant cell arteritis	CCL2 CHI3L1 CSF2 DLL1 ELN FCGR2A FCGR3A HLA-DRB1 IFNG IL17A IL21R IL4 JAG1 MBL2 MFGE8 MMP2 MMP9 TLR4	1116 1437 182 2006 2212 2214 28514 3123 3458 3565 3605 4153 4240 4313 4318 50615 6347 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:4183	pseudopseudohypoparathyroidism Aliases: Normocalcemic pseudohypoparathyroidism	Gnas	14683	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3770	pulmonary fibrosis Aliases: Fibrosis of lung	Ace Agt B3gat1 Bad Bdkrb1 Bdnf Ccl11 Ccl2 Ccr5 Cdh1 Chi3l1 Chrm3 Col1a1 Col1a2 Csf2 Cysltr1 Dnm1l Hgf Hsp90ab1 Hspd1 Icam1 Igfbp3 Il13 Il15 Il1a Il1rn Il4 Jag1 Mmp9 Nfe2l2 Ngf Notch1 Pdgfra Ptgs2 Serpine1 Sftpa1 Sftpb Tfpi Tgfb1 Tgfbr2 Timp1 Tnf	114099 114114 116510 116553 116630 117029 117108 192155 24179 24225 24260 24310 24446 24484 24493 24617 24770 24773 24835 25267 25464 25496 25670 287287 29146 29393 29397 29436 29527 301252 310738 59086 60582 63868 64639 81509 81687 81810 83502 83619 84352 89824	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:893	Wilson disease Aliases: Cerebral pseudosclerosis Westphal pseudosclerosis Westphal-Strumpell syndrome Wilson's disease hepatolenticular degeneration	ANXA5 ATP7A ATP7B CP CYP27B1 HMGCR SMPD1	1356 1594 308 3156 538 540 6609	Homo sapiens (human)	Alliance of Genome Resources
DOID:3025	acinar cell carcinoma Aliases: acinic cell carcinoma	APC	324	Homo sapiens (human)	Alliance of Genome Resources
DOID:9470	bacterial meningitis	Ache Bdnf Cd46 Chi3l1 Crp Mmp9 Ngf Parp1	24225 25419 25591 29333 310738 81687 83817 89824	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2772	irritant dermatitis Aliases: irritant contact dermatitis primary irritant dermatitis	Il4	16189	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11198	DiGeorge syndrome Aliases: 22q11.2 deletion syndrome DiGeorge sequence DiGeorge's syndrome Pharyngeal pouch syndrome	ALDH1A2 CHRD CRKL DICER1 DOCK1 DVL1 ESS2 FGF8 HOXA3 KAT6A NDST1 PLXND1 TGFBR2 UFD1 VEGFA	1399 1793 1855 2253 23129 23405 3200 3340 7048 7353 7422 7994 8220 8646 8854	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110142	Bartter disease type 1 Aliases: BARTS1 Bartter syndrome type 1 Bartter syndrome type 1 antenatal hyperprostaglandin E syndrome 1 hypokalemic alkalosis with hypercalciuria 1 antenatal	SLC12A1	6557	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080560	congenital disorder of glycosylation Ih Aliases: congenital disorder of glycosylation 1h	ALG8	854233	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1188	mononeuropathy	GAL	51083	Homo sapiens (human)	Alliance of Genome Resources
DOID:3310	atopic dermatitis Aliases: Atopic neurodermatitis Besnier's prurigo allergic dermatitis atopic eczema	adm-4 asp-17 lev-9	180250 181041 188252	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0060646	congenital chylothorax	ItgaPS4 ItgaPS5 scb	36692 36693 37732	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4257	Caffey disease Aliases: cortical congenital hyperostosis infantile cortical hyperostosis	Col1a1	29393	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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