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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 **5076 - 5100** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:2170	vaginitis	ABO CTNS GALNS GLA LYZ MBL2	1497 2588 2717 28 4069 4153	Homo sapiens (human)
DOID:13003	vertebrobasilar insufficiency Aliases: Vertebro-basilar insufficiency Vertebrobasilar arterial insufficiency Vertebrobasilar artery syndrome	ACE CALR CAT CD74 CHKA CYP2C19 DHCR24 FCN1 G6PD GLA GPX3 ICAM1 LTC4S MCFD2 NAMPT OGG1 OLR1 PARP1 PIGA PIK3CA PIK3CB PIK3CD PIK3CG PLA2G7 PTEN PTGS2 SELL SELP SIRT6 SMPD3 SULT1E1	10135 1119 142 1557 1636 1718 2219 2539 2717 2878 3383 4056 4968 4973 51548 5277 5290 5291 5293 5294 55512 5728 5743 6402 6403 6783 7941 811 847 90411 972	Homo sapiens (human)
DOID:0110771	hereditary spastic paraplegia 18 Aliases: IDMDC SPG18 autosomal recessive spastic paraplegia 18 autosomal recessive spastic paraplegia type 18 intellectual disability, motor dysfunction and joint contractures	B4GALNT1 CYP2B6 CYP2U1 CYP39A1 CYP7B1 FAR1 GBA2 L1CAM MAG PCYT2 PLA2G6 PNPLA6 SELENOI SLC33A1 ST3GAL5	10908 113612 1555 2583 3897 4099 51302 57704 5833 8398 84188 85465 8869 9197 9420	Homo sapiens (human)
DOID:0111263	combined malonic and methylmalonic acidemia Aliases: CMAMMA combined malonic and methylmalonic aciduria	ACSF3	197322	Homo sapiens (human)
DOID:0070437	hyperphosphatasia with impaired intellectual development syndrome 6 Aliases: GPIBD40 HPMRS4 glycosylphosphatidylinositol biosynthesis defect 40 hyperphosphatasia with mental retardation syndrome 4	PIGY	84992	Homo sapiens (human)
DOID:9261	nasopharynx carcinoma Aliases: Nasopharyngeal carcinoma malignant Nasopharyngeal tumor malignant neoplasm of nasopharynx nasopharynx cancer	Mapk14 Trp53	22059 26416	Mus musculus (house mouse)
DOID:4137	common bile duct disease	Slc25a13	50799	Mus musculus (house mouse)
DOID:0070468	Yoon-Bellen neurodevelopmental syndrome Aliases: YOBELN	OGDH OGDHL	4967 55753	Homo sapiens (human)
DOID:13452	scleritis	Tnf	24835	Rattus norvegicus (Norway rat)
DOID:0060714	autosomal recessive congenital ichthyosis 5 Aliases: ARCI5 autosomal recessive congenital nonlamellar and nonerythrodermic ichthyosis	ALDH3A2 ALOX12B CERS3 COG7 CYP2B6 GBA1 STS SULT2B1	1555 204219 224 242 2629 412 6820 91949	Homo sapiens (human)
DOID:4989	pancreatitis	Htr2a Lepr Tlr2 Tlr4	15558 16847 21898 24088	Mus musculus (house mouse)
DOID:0112361	spondylocostal dysostosis 3 Aliases: SCDO3 autosomal recessive spondylocostal dysostosis 3	lfng	30158	Danio rerio (zebrafish)
DOID:3498	pancreatic ductal adenocarcinoma Aliases: ductal adenocarcinoma of the pancreas	ABO ACACB ACE AKR1B10 AKR7A2 APRT ARSA ATP6AP2 B3GALNT1 CALR CD44 CEACAM5 CEACAM6 CEL CEMIP CHGA CHKA CHST15 COL9A2 CYP1B1 CYP3A5 CYP4F2 CYP4F3 DAG1 DPEP1 ENO1 FASN FBP1 FCN2 FOLR1 FOLR2 FUT8 GALNT5 GOLPH3 GOT1 GPC1 GPC5 HK1 IDH1 IDUA L1CAM LGALS1 LGALS3 LGALS4 MDH1 MMUT MRC1 MSLN MUTYH NAMPT NEU2 NT5E PAFAH1B2 PARP1 PDHX PGAM1 PGK1 PIK3CA PIK3CB PIK3CD PIK3CG PKM PLD1 PNPLA2 PRKAA2 PRNP PTEN PTGS2 RECK REG3G SIGLEC7 SIRT6 SMUG1 SOAT1 ST6GAL1 VCAM1 VNN1	10135 10159 10232 1048 1056 1113 1119 11227 1298 130120 142 1545 1577 1605 1636 1800 2023 2194 2203 2220 2262 2348 2350 23583 2530 27036 28 2805 2817 3098 32 3417 3425 353 3897 3956 3958 3960 4051 410 4190 4360 4594 4595 4680 4759 4907 5049 51363 51548 5223 5230 5290 5291 5293 5294 5315 5337 5563 5621 57016 57104 57214 5728 5743 64083 6480 6646 7412 8050 811 8434 8529 8574 8706 8876 960	Homo sapiens (human)
DOID:310	MERRF syndrome Aliases: Fukuhara syndrome Myoclonic epilepsy - ragged red fibers Myoclonus epilepsy AND ragged red fibers Myoclonus with epilepsy and with Ragged Red Fibers	CLN5 EPM2A	1203 7957	Homo sapiens (human)
DOID:10223	dermatomyositis Aliases: Polymyositis with skin involvement dermatopolymyositis	Tl	43222	Drosophila melanogaster (fruit fly)
DOID:885	fascioliasis Aliases: Fasciola hepatica infection Infection by Fasciola Liver flukes Sheep liver fluke infection	HPGDS PSAP SLC17A5	26503 27306 5660	Homo sapiens (human)
DOID:6498	seborrheic keratosis	Pik3ca	18706	Mus musculus (house mouse)
DOID:3650	lactic acidosis	Dlat Pygl	64035 81654	Rattus norvegicus (Norway rat)
DOID:0110370	retinitis pigmentosa 55 Aliases: RP55	Arl6	56297	Mus musculus (house mouse)
DOID:0050559	Fukuyama congenital muscular dystrophy	fktn.S	495324	Xenopus laevis (African clawed frog)
DOID:9296	cleft lip Aliases: Labium leporinum cheiloschisis cleft lip, unilateral, complete complete unilateral cleft lip hare lip	Sdc rt	37447 39297	Drosophila melanogaster (fruit fly)
DOID:12377	spinal muscular atrophy	Hexb	15212	Mus musculus (house mouse)
DOID:9849	Meniere's disease Aliases: Meniere disease Mnire's vertigo Otogenic vertigo	FCGR3B HPGDS MICA NT5E PARP1	100507436 142 2215 27306 4907	Homo sapiens (human)
DOID:4249	Gerstmann-Straussler-Scheinker syndrome Aliases: Gerstmann-Straussler-Scheinker disease PRION DEMENTIA	ACHE APRT CYP7A1 G6PC1 GBE1 GYG1 GYS2 MDH1 MGAM PRNP PYGL PYGM SI SLC37A4	1581 2538 2542 2632 2992 2998 353 4190 43 5621 5836 5837 6476 8972	Homo sapiens (human)
DOID:0060786	hypomyelinating leukodystrophy Aliases: HLD	DEGS1	8560	Homo sapiens (human)

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