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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 **3626 - 3650** of **4649** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:2340	craniosynostosis Aliases: Premature closure of cranial sutures	ALX4 BBS9 FGFR2 FGFR3 FLNA NELL1 NOG SKI TCF12 TWIST1	2261 2263 2316 27241 4745 60529 6497 6938 7291 9241	Homo sapiens (human)	Alliance of Genome Resources
DOID:2344	polyclonal hypergammaglobulinemia	COPG1	22820	Homo sapiens (human)	Alliance of Genome Resources
DOID:2349	arteriosclerosis Aliases: Arteriosclerotic vascular disease	ABCG5 ABCG8 ACAT1 AKR1B1 ALDH3A1 ALOX5 ALPL APOA1 APOB APOH B2M CCL5 CD36 CDH13 CHI3L1 EGR1 ESR1 F13A1 F7 FURIN HGF HP HSPD1 IFNGR1 IGFBP3 IL10 IL15 IL6ST ITGA2 ITGA7 KDR LCAT LDLR LEPR LMNA LOX MAP3K7 MET MMP12 MMP13 MMP14 MMP1 MMP2 MMP3 MMP9 MSR1 NME2 NOTCH4 NPPC PAPPA PON1 PPARG PTGER4 PTGS2 RELA SERPINA1 TBXAS1 TGFB1 TGFBR2 TLR4 TNFRSF14	1012 1116 1958 2099 2155 2162 218 231 240 249 3082 3240 3329 335 338 3459 3486 350 3572 3586 3600 3673 3679 3791 38 3931 3949 3953 4000 4015 4233 4312 4313 4314 4318 4321 4322 4323 4481 4831 4855 4880 5045 5069 5265 5444 5468 567 5734 5743 5970 6352 64240 64241 6885 6916 7040 7048 7099 8764 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:2352	hemochromatosis Aliases: Haemochromatosis diabetes bronze iron storage disorder	B2M HFE HJV TFR2 TNF	148738 3077 567 7036 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:2355	anemia Aliases: anaemia	ACE ANK1 APC BMP6 EPO EPOR G6PD GDF15 GPX1 HBB HK1 IL10 IREB2 PON1 SLC11A2 SLC4A10 SLC4A11 SLC4A1 SLC4A2 SLC4A4 SLC4A5 SLC4A7 SLC4A8 SLC4A9 TF TNF TNFRSF1A VCAM1	1636 2056 2057 2539 286 2876 3043 3098 324 3586 3658 4891 5444 57282 57835 6521 6522 654 7018 7124 7132 7412 83697 83959 8671 9497 9498 9518	Homo sapiens (human)	Alliance of Genome Resources
DOID:2361	macrocytic anemia Aliases: ANEMIA MACROCYTIC Macrocytic anaemia	KIT	3815	Homo sapiens (human)	Alliance of Genome Resources
DOID:2366	West Nile fever	CCR5 KIR3DS1 RFC1	1234 3813 5981	Homo sapiens (human)	Alliance of Genome Resources
DOID:2367	neuroaxonal dystrophy	NAGA PLA2G6	4668 8398	Homo sapiens (human)	Alliance of Genome Resources
DOID:2373	hereditary elliptocytosis Aliases: Congenital elliptocytosis ovalocytosis	EPB41 SLC4A1	2035 6521	Homo sapiens (human)	Alliance of Genome Resources
DOID:2377	multiple sclerosis Aliases: Generalized multiple sclerosis insular sclerosis	A2M ACAN ACHE ADIPOQ AGER AGT APOA1 APOC2 B4GALT5 B4GALT6 BDNF CACNA1B CCL1 CCL2 CCL5 CCL7 CCR3 CCR5 CD24 CD28 CD40 CD46 CD86 CIITA CLEC16A COL1A1 CTLA4 CTSB EDN1 FAS FASLG FCGR2A FCGR3A GABRA3 GC GLI1 GRM8 GRN H6PD HDAC1 HLA-DPB1 HLA-DQA1 HLA-DQB1 HLA-DRA HLA-DRB1 HLA-DRB3 HSP90AB1 HSPA8 IFNB1 IFNG IGF2 IL13 IL17A IL21R IL23R IL2RA IL4 IL4R IL6 IRF5 JAG1 KIF1B LRCH1 MAG MBP MMP12 MMP9 MOG MPHOSPH9 NECTIN2 NEFH NEFL NGFR NOTCH4 PDCD1 PHACTR2 PLA2G7 PRF1 PTPRC RGMA RHOA SHH SLC11A1 SPP1 TLR4 TNF TNFRSF1A	100133941 10198 1232 1234 1277 149233 1493 1508 176 177 182 183 1906 2 2212 2214 23095 23143 23274 2556 2638 2735 2896 2918 3065 3115 3117 3119 3122 3123 3125 3312 3326 335 344 3456 3458 3481 355 3559 356 3565 3566 3569 3596 3605 3663 387 4099 4155 4179 4261 43 4318 4321 4340 4744 4747 4804 4855 50615 5133 5551 56963 5788 5819 627 6346 6347 6352 6354 6469 6556 6696 7099 7124 7132 774 7941 9331 9334 9370 940 942 9563 958 9749	Homo sapiens (human)	Alliance of Genome Resources
DOID:2378	relapsing-remitting multiple sclerosis Aliases: RRMS Relapsing-remitting MS	ADAMTS14 APOA4 CD36 CD80 CSPG4 CTSS FAS GRN HAVCR1 HSPA8 MMP19 MMP9 NEFH NEFL NOD2 NOG SERPINE1 TIMP1	140766 1464 1520 26762 2896 3312 337 355 4318 4327 4744 4747 5054 64127 7076 9241 941 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:2383	neonatal jaundice Aliases: neonatal hyperbilirubinemia neonatal icterus	G6PD	2539	Homo sapiens (human)	Alliance of Genome Resources
DOID:2384	Wernicke encephalopathy Aliases: Wernicke's disease Wernicke's encephalopathy	FOS PTGS2	2353 5743	Homo sapiens (human)	Alliance of Genome Resources
DOID:2388	renal artery disease Aliases: renal vascular disease vascular disorder of kidney	EDN1	1906	Homo sapiens (human)	Alliance of Genome Resources
DOID:2394	ovarian cancer Aliases: malignant Ovarian tumor malignant tumour of ovary ovarian neoplasm ovary neoplasm primary ovarian cancer tumor of the Ovary	ABCB1 AKT1 ANGPT1 ANXA7 APC APEX1 APOB BARD1 BRCA1 BRCA2 CALR CBS CCN2 CD59 CD82 CD9 CDH13 CDH1 CHI3L1 COMT CRKL CTNNB1 CYP19A1 DDR1 EEF1A2 EFEMP2 EGF ERBB2 ESR1 F2 F7 FAS FGF7 HDAC3 HFE HIF1A ICAM1 IL10 ITGA8 JAK1 JUP KLK10 KLK4 KLK6 LEF1 MBL2 MET MMP1 MMP8 MRE11 MSH6 MSLN MUC16 MYO6 NASP NBN NME1 NME2 NOD2 NOS3 NRG1 OGG1 OPCML PEBP1 PECAM1 PIK3CA POLE PRKCA PRSS8 PTEN PTGS1 RUNX3 SERPINC1 SFN SHMT1 SLCO1B3 SMAD4 SOD2 SPINT1 STAT3 TBX3 TFF1 TFRC TIMP1 TNF TNFRSF1A TNFRSF1B TYMP UGT1A1 UTRN VEGFC YAP1	1012 10232 10413 1116 1312 1399 1490 1499 1588 1890 1917 1950 2064 207 2099 2147 2155 2252 2810 28234 284 2956 30008 3077 3084 3091 310 324 328 338 3383 355 3586 3716 3728 3732 4089 4153 4233 4312 4317 4361 462 4646 4678 4683 4830 4831 4846 4968 4978 5037 51176 5175 5243 5290 5426 54658 5578 5652 5653 5655 5728 5742 580 64127 6470 6648 6692 672 675 6774 6926 7031 7037 7076 7124 7132 7133 7402 7424 780 811 8516 864 875 8841 928 94025 9622 966 999	Homo sapiens (human)	Alliance of Genome Resources
DOID:2431	glomus tumor Aliases: Glomus neoplasm Glomus tumour	GLMN	11146	Homo sapiens (human)	Alliance of Genome Resources
DOID:2436	glomangioma Aliases: Glomuvenous Malformation	GLMN	11146	Homo sapiens (human)	Alliance of Genome Resources
DOID:2450	central retinal vein occlusion	PROC SERPINF1	5176 5624	Homo sapiens (human)	Alliance of Genome Resources
DOID:2451	protein S deficiency Aliases: Protein S deficiency disease	PROS1 TFPI	5627 7035	Homo sapiens (human)	Alliance of Genome Resources
DOID:2452	thrombophilia Aliases: hypercoagulability state	CD46 F2 FGA HLA-DQA1 PLG PROC SERPINA10 THBD	2147 2243 3117 4179 51156 5340 5624 7056	Homo sapiens (human)	Alliance of Genome Resources
DOID:2468	psychotic disorder Aliases: mental or behavioural disorder	MT2A NRG1	3084 4502	Homo sapiens (human)	Alliance of Genome Resources
DOID:2475	chronic conjunctivitis	FAS LAMP2	355 3920	Homo sapiens (human)	Alliance of Genome Resources
DOID:2476	hereditary spastic paraplegia Aliases: French settlement disease Strumpell-Lorrain disease familial spastic paraplegia hereditary spastic paraparesis	ALDH18A1 AP5Z1 ATL2 ATL3 ATP13A2 ATP13A3 ATP13A5 BSCL2 CAPN1 CAPN3 DNM1 DNM2 ERLIN1 ERLIN2 HSPD1 KIF5B L2HGDH NIPAL1 NIPAL4 PNPLA6 PNPLA7 PSMC4 RTN1 RTN2 RTN3 RTN4 SEC23IP SPAST	10313 10613 10908 11160 11196 152519 1759 1785 23400 25923 26580 3329 344905 348938 375775 3799 5704 57142 5832 6252 6253 64225 6683 79572 79944 823 825 9907	Homo sapiens (human)	Alliance of Genome Resources
DOID:2477	motor peripheral neuropathy Aliases: HSMN HSMN - Hereditary sensory and motor neuropathy Hereditary motor and sensory neuropathy Peripheral Motor Neuropathy neuropathic muscular atrophy	EGR2 SLC12A6	1959 9990	Homo sapiens (human)	Alliance of Genome Resources
DOID:2490	congenital nervous system abnormality Aliases: congenital neurologic anomaly	TUBA1A	7846	Homo sapiens (human)	Alliance of Genome Resources

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