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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 **6226 - 6250** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0050771	pheochromocytoma Aliases: phaeochromocytoma	Nrg	31792	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0110444	dilated cardiomyopathy 1X Aliases: CMD1X dilated cardiomyopathy with mild or no proximal muscle weakness	FKTN	2218	Homo sapiens (human)	Glyco-Disease Genes Database Alliance of Genome Resources
DOID:0110682	congenital myasthenic syndrome 16 Aliases: CMS16 congenital myasthenic syndrome acetazolamide-responsive	Scn4a	25722	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0080567	congenital disorder of glycosylation Ip Aliases: congenital disorder of glycosylation 1p	alg11.L alg11.S	108709929 733388	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:1934	dysostosis	EFNB1 KIF3A	11127 1947	Homo sapiens (human)	Alliance of Genome Resources
DOID:2527	nephrosis	ACE ANGPT1 ANGPT2 CAT CCL1 CCL7 CD36 CD59 CFH CX3CL1 CYP11A1 CYP27B1 EDN1 F2 GATA3 GPX1 HAVCR1 LAMB2 LRP2 NES NPPA NPPB PDPN PTPRU SREBF2 VIM	10076 10630 10763 1583 1594 1636 1906 2147 2625 26762 284 285 2876 3075 3913 4036 4878 4879 6346 6354 6376 6721 7431 847 948 966	Homo sapiens (human)	Alliance of Genome Resources
DOID:3087	gingivitis Aliases: acute gingivitis chronic gingivitis	FMOD IL6 VEGFA	2331 3569 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090034	myoclonic dystonia 11	SGCE	8910	Homo sapiens (human)	Alliance of Genome Resources
DOID:1459	hypothyroidism Aliases: Thyroid deficiency Thyroid insufficiency	C14B9.8 W01C8.5 bli-3 cts-1 cwn-1 daf-7 duox-2 gpx-3 gpx-5 grd-2 lad-2 ncam-1 pbo-4 pgal-1 wrt-6	171608 172108 173399 175237 176149 176437 177078 180349 180418 180638 180836 181178 181285 182513 186188	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110218	Brugada syndrome 1 Aliases: BRGDA1	Scn5a	20271	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3382	liposarcoma Aliases: lipomatous cancer	FUS IL22	2521 50616	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060917	facioscapulohumeral muscular dystrophy 3 Aliases: FSHD3 facioscapulohumeral muscular dystrophy type 3	LRIF1	55791	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111731	familial episodic pain syndrome 3 Aliases: FEPS3	para	32619	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0070204	familial partial lipodystrophy type 3 Aliases: FPLD3 PPARG-related FPLD PPARG-related familial partial lipodystrophy familial partial lipodystrophy associated with PPARG mutations	Pparg	19016	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080600	COVID-19 Aliases: 2019 Novel Coronavirus (2019-nCoV) 2019-nCoV infection COVID19 SARS-CoV-2 infection Wuhan coronavirus infection Wuhan seafood market pneumonia virus infection	Acer Ance-3 Ance Spn28Dc fw sca	32162 34091 34189 34805 34808 36411	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4752	multiple system atrophy Aliases: Shy-Drager syndrome	Ambra1 Coq2 Fas Igf2 Slc1a1 Slc6a6 Snca	14102 16002 20510 20617 21366 228361 71883	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1682	congenital heart disease Aliases: Congenital Heart Defects Congenital anomaly of heart Heart Malformation congenital heart defect heart defect	gdf3 jag1a notch1a tll1 vegfaa	140421 30125 30682 30718 474335	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0060500	drug allergy	IL2	3558	Homo sapiens (human)	Alliance of Genome Resources
DOID:11829	degenerative myopia Aliases: degenerative progressive high myopia pathological myopia progressive high (degenerative) myopia progressive high myopia	HLA-DQB1 LRP2	3119 4036	Homo sapiens (human)	Alliance of Genome Resources
DOID:1094	attention deficit hyperactivity disorder Aliases: ADHD attention deficit disorder hyperkinetic disorder	Adgre1 Adgrl1 Adgrl2 Adgrl3 Adgrl4 Adra2a Baiap2 Bdnf Brinp1 Cdh2 Chrnb2 Comt Csnk1d Dbh Drd4 Drd5 Git1 Grin2b Grm8 Hmgcr Htr1b Mef2c Mef2d Mmp9 Nf1 Ntrk2 Per1 Ptchd1 Slc6a2 Slc6a3 Slc6a4 Snap25 Tacr1 Ust Vegfa	104318 108100 11444 11551 12064 12558 12846 13162 13166 13491 13492 13733 14812 14823 15357 15551 15567 170757 17260 17261 17395 18015 18212 18626 20538 20614 211612 21336 216963 22339 319387 330814 338362 56710 99633	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111541	pigmented paravenous chorioretinal atrophy Aliases: PPRCA	Crb1	170788	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111166	molybdenum cofactor deficiency type C Aliases: MOCOD type C MOCODC combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C molybdenum cofactor deficiency complementation group C	Gphn	268566	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111134	focal segmental glomerulosclerosis 9 Aliases: FSGS9	Crb2	241324	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111130	focal segmental glomerulosclerosis 5 Aliases: FSGS5	INF2	64423	Homo sapiens (human)	Alliance of Genome Resources
DOID:11589	Riley-Day syndrome Aliases: HSAN III familial autonomic nervous dysfunction familial dysautonomia	Elp1	230233	Mus musculus (house mouse)	Alliance of Genome Resources

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