GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Display
results per page.

Clear

Submissions

GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **6051 - 6075** of **7942** in total

« First

‹ Prev

…

239

240

241

242

243

244

245

246

247

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:0111242	congenital muscular dystrophy-dystroglycanopathy type A6 Aliases: MDDGA6 Walker-Warburg syndrome or muscle-eye-brain disease, LARGE-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A6	large1	100498555	Xenopus tropicalis (tropical clawed frog)
DOID:1470	major depressive disorder Aliases: clinical depression major depression recurrent major depression single major depressive episode unipolar depression	Htr2a	29595	Rattus norvegicus (Norway rat)
DOID:0070516	Mitchell syndrome	ACOX1	51	Homo sapiens (human)
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	pomt2.L	108698684	Xenopus laevis (African clawed frog)
DOID:11202	primary hyperparathyroidism Aliases: familial primary hyperparathyroidism	ACE ALPP APRT ATRNL1 CYP19A1 KL MCAT PTGS2 SDHC	1588 1636 250 26033 27349 353 5743 6391 9365	Homo sapiens (human)
DOID:2685	ossifying fibromyxoid tumor Aliases: Ossifying Fibromyxoma ossifying fibromyxoid tumour	ENO2	2026	Homo sapiens (human)
DOID:0060041	autism spectrum disorder	ext1a ext1b ndst1a ndst1b ndst2a ndst2b ndst3	100317129 100329944 497279 497280 570459 793524 798226	Danio rerio (zebrafish)
DOID:11446	sciatic neuropathy	Gsk3b Hmgb1 Kcnj11 Pcna Ppargc1a Tlr4 Tnf	24835 25459 25737 29260 83516 83535 84027	Rattus norvegicus (Norway rat)
DOID:11984	hypertrophic cardiomyopathy Aliases: hypertrophic obstructive cardiomyopathy	Cs	170587	Rattus norvegicus (Norway rat)
DOID:12930	dilated cardiomyopathy Aliases: primary dilated cardiomyopathy	cs fkrp	100145309 550067	Xenopus tropicalis (tropical clawed frog)
DOID:841	extrinsic allergic alveolitis Aliases: alveolitis hypersensitivity pneumonitis	Tnf	24835	Rattus norvegicus (Norway rat)
DOID:0111275	speech-language disorder-1 Aliases: CAS articulatory apraxia childhood apraxia of speech developmental apraxia of speech developmental verbal dyspraxia speech and language disorder with orofacial dyspraxia speech-language disorder type 1	ACE ALDH2 B3GAT1 CHI3L1 FASN FCGR3B GALT LGALS1	1116 1636 217 2194 2215 2592 27087 3956	Homo sapiens (human)
DOID:9181	amebiasis Aliases: amoebiasis entamoebiasis	PIK3CA PIK3CB PIK3CD PIK3CG	5290 5291 5293 5294	Homo sapiens (human)
DOID:0090137	complex cortical dysplasia with other brain malformations 1 Aliases: CDCBM1 cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation	ATP6V0A2 ATP6V1A B3GALNT2 B4GAT1 CRPPA DAG1 DHCR24 DLST FIG4 FKRP FKTN HSPG2 LARGE1 NSDHL PAFAH1B1 PIGP PIGQ POMGNT1 POMGNT2 POMK POMT1 POMT2 RXYLT1 SDC2 STS TMTC3	10329 10585 11041 148789 160418 1605 1718 1743 2218 23545 29954 3339 412 5048 50814 51227 523 55624 6383 729920 79147 84197 84892 9091 9215 9896	Homo sapiens (human)
DOID:0080512	Meier-Gorlin syndrome 1	ACHE CLEC7A COMT CYP4F3 FASN LYZ PIK3CA PIK3CG PLA2G4A PLCB1	1312 2194 23236 4051 4069 43 5290 5294 5321 64581	Homo sapiens (human)
DOID:170	endocrine gland cancer Aliases: Endocrine tumor endocrine neoplasm malignant Endocrine tumor malignant neoplasm of endocrine gland malignant tumour of endocrine gland neoplasm of endocrine gland neoplasm of endocrine system	CHGA PTEN SDHB SDHC	1113 5728 6390 6391	Homo sapiens (human)
DOID:7398	cerebral primitive neuroectodermal tumor Aliases: PNET of Cerebrum	ABO AMACR CD38 CHGA ENO2 HMMR HPGDS MELTF MRC1 PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGS2 SIGLEC7 UGCG	1113 2026 23600 27036 27306 28 3161 4241 4360 5290 5291 5293 5294 5728 5743 7357 952	Homo sapiens (human)
DOID:2513	basal cell carcinoma Aliases: Basal cell cancer Basal cell carcinoma of skin Basal cell neoplasm Basal cell tumor Epithelioma basal cell Rodent ulcer malignant Basal cell neoplasm malignant basal cell tumor	ACE ACSL5 BAAT CAT CD38 CD44 CD74 CDH13 CEACAM5 CHKA CLEC4G COLEC10 CYP19A1 CYP1A1 CYP1B1 CYP24A1 CYP27A1 CYP27B1 CYP2B6 CYP2R1 DCN FASN GALNT14 GAPDH GPC3 HAS1 HAS3 HPGDS HPSE HSD17B7 HYAL3 ICAM1 KLRK1 LGALS1 LGALS3 LYPD5 MICA MMUT MRC1 NAMPT NCAM1 NEIL3 NEU1 NT5E NTHL1 OGG1 PGP PIK3CA PIK3CB PIK3CD PIK3CG PLAUR PLD2 PPT1 PRKAA2 PTEN PTGS1 PTGS2 RGMA SC5D SCD SDC1 SIRT2 SIRT6 SMUG1 SOAT1 TEX101 TNKS2 TP53 TYMP UMPS	100507436 1012 10135 1048 10584 10855 1119 120227 1543 1545 1555 1588 1591 1593 1594 1634 1636 1890 2194 22914 22933 23583 2597 2719 27306 283871 284348 3036 3038 3383 339390 3956 3958 4360 4594 4684 4758 4907 4913 4968 51478 51548 51703 5290 5291 5293 5294 5329 5338 55247 5538 5563 56963 570 5728 5742 5743 6309 6319 6382 6646 7157 7372 79623 80351 83639 8372 847 952 960 972	Homo sapiens (human)
DOID:3633	beta-mannosidosis Aliases: Beta-D-mannosidosis beta-mannosidase deficiency lysosomal beta-mannosidase deficiency	Manba	110173	Mus musculus (house mouse)
DOID:971	tendinitis	ABO ACAN ACLY ADH1B B3GALT6 CD14 CD44 CHAT CYP19A1 DCN ENPP1 EXT1 EXT2 EXTL3 FMOD HPSE HSPG2 IDH1 IDH2 KL LRP5 PRNP PTEN PTGIS SIGLEC7 VCAN	10855 1103 125 126792 1462 1588 1634 176 2131 2132 2137 2331 27036 28 3339 3417 3418 4041 47 5167 5621 5728 5740 929 9365 960	Homo sapiens (human)
DOID:6406	double outlet right ventricle Aliases: Dextrotransposition of aorta Double outlet right ventricle with subpulmonary ventricular septal defect Taussig-Bing syndrome or defect	CERS1 CFC1 COMT DGCR2 GPC3 NT5E PTEN PTGS2 TMEM260 UGCG	10715 1312 2719 4907 54916 55997 5728 5743 7357 9993	Homo sapiens (human)
DOID:10983	Alport syndrome Aliases: Hereditary Nephritis	ACE ACSL4 B3GAT1 CYP24A1	1591 1636 2182 27087	Homo sapiens (human)
DOID:0080208	metabolic dysfunction-associated steatotic liver disease Aliases: MAFLD MASLD NAFLD metabolic dysfunction-associated fatty liver disease metabolic dysfunction-related steatotic liver disease metabolic-associated fatty liver disease non-alcoholic fatty liver disease nonalcoholic fatty liver disease	dgat2	395003	Xenopus tropicalis (tropical clawed frog)
DOID:0110672	congenital myasthenic syndrome 21 Aliases: CMS21 congenital myasthenic syndrome 21, presynaptic	CHAT	1103	Homo sapiens (human)
DOID:0111181	familial hemiplegic migraine 1 Aliases: FHM1 MHP1 familial hemiplegic migraine1 with progressive cerebellar ataxia	PMM2 PRKCSH	5373 5589	Homo sapiens (human)

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements