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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 **13451 - 13475** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▼	Organism	Source
DOID:5453	pulmonary venoocclusive disease Aliases: pulmonary veno-occlusive disease	Atf4 Eif2ak3 Kcnk3	11911 13666 16527	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4930	nasal cavity adenocarcinoma Aliases: adenocarcinoma of the nasal cavity	CLU	1191	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060449	gelatinous drop-like corneal dystrophy Aliases: GDCD corneal amyloidosis primary familial amyloidosis of the cornea subepithelial amyloidosis of the cornea	CLU TACSTD2	1191 4070	Homo sapiens (human)	Alliance of Genome Resources
DOID:4251	conjunctival disease	CLU IL6 TNFAIP6	1191 3569 7130	Homo sapiens (human)	Alliance of Genome Resources
DOID:11656	cicatricial pemphigoid Aliases: Cicatricial pemphigoid with ocular involvement Ocular pemphigoid benign mucous membrane pemphigoid benign mucous membrane pemphigoid with ocular involvement ocular pemphigus	CLU HLA-DQB1 HLA-DRB1 IL1RN TNF	1191 3119 3123 3557 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050426	Stevens-Johnson syndrome	CLU HLA-A HLA-B HLA-DQB1 TNF	1191 3105 3106 3119 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:8691	mycosis fungoides Aliases: mycosis fungoides lymphoma	CLU HIF1A HLA-DQB1 SOD2	1191 3091 3119 6648	Homo sapiens (human)	Alliance of Genome Resources
DOID:4449	macular retinal edema Aliases: macular edema macular oedema macular retinal oedema	APOH CCL2 CLU EPO FLT1 HIF1A IL6 KDR NOS3 SERPINF1 VEGFA	1191 2056 2321 3091 350 3569 3791 4846 5176 6347 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:3429	inclusion body myositis	CCR2 CD36 CLU DAG1 FAS MYH15 MYH1 MYH7 SOD2 VCP	1191 1605 22989 355 4619 4625 6648 729230 7415 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:4780	anti-basement membrane glomerulonephritis Aliases: anti-GBM glomerulonephritis	AGT AGTR1 BAX CCL2 CCL5 CD40LG CD80 CLU CSF1 CSF1R CTLA4 CX3CL1 FCGR3A HLA-DPB1 HLA-DRB1 IL10 IL17A IL1RN IL4 ITGA4 MAPK14 MIF MMP12 MMP14 NOS2 PDCD1 SELP SLIT2 SYK TNF	1191 1432 1435 1436 1493 183 185 2214 3115 3123 3557 3565 3586 3605 3676 4282 4321 4323 4843 5133 581 6347 6352 6376 6403 6850 7124 9353 941 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080000	muscular disease	ACACA ACACB CLU CPT2 FASN HMGCR ITGA7 LPL	1191 1376 2194 31 3156 32 3679 4023	Homo sapiens (human)	Alliance of Genome Resources
DOID:11555	Fuchs' endothelial dystrophy Aliases: FCED Fuchs' corneal dystrophy Fuchs' endothelial corneal dystrophy	AGBL1 C3 CLU COL8A2 LOXHD1 SLC4A11 TCF4 ZEB1	1191 123624 125336 1296 6925 6935 718 83959	Homo sapiens (human)	Alliance of Genome Resources
DOID:13378	Kawasaki disease Aliases: Kawasaki's disease MLNS acute febrile MCLS acute febrile mucocutaneous lymph node syndrome mucocutaneous lymph node syndrome	ADIPOQ AGER BTNL2 CCR2 CCR5 CD40 CD40LG CLU FLT1 HMGB1 HP HSPA1A HSPA1L MBL2 MMP9 NPPB SELP TIMP1 TLR4 TNF VEGFA	1191 1234 177 2321 3146 3240 3303 3305 4153 4318 4879 56244 6403 7076 7099 7124 729230 7422 9370 958 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:2256	osteochondrodysplasia Aliases: Cartilage Development disorder Congenital anomaly of cartilage Osteochondrodysplasia syndrome chondrodystrophy skeletal dysplasia	Atf2 Cebpb Chst3 Col11a2 Col2a1 Comp Flnb Hspg2 Lifr Matn3 Pth1r Rnf146 Ryr1 Slc26a2 Tgfb1 Tgfb2 Tgfbr1	11909 12608 12815 12824 12845 13521 15530 16880 17182 19228 20190 21803 21808 21812 286940 53374 68031	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080322	polycystic kidney disease	Atf1 C9 Ctsb Ctsh Dll4 Ganab Gnas Gpbar1 Kif3a Mtor Myc Nos3 Pkd1 Pkd2 Pla2g4a Pparg Ptgs1 Ptgs2 Ptma Sod1 Stam2 Stam Tnc Xylt2	11908 12279 13030 13036 14376 14683 16568 17869 18127 18763 18764 18783 19016 19224 19225 19231 20655 20844 217119 21923 227289 54485 56324 56717	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3755	antithrombin III deficiency Aliases: AT III deficiency hereditary thrombophilia due to congenital antithrombin deficiency	Serpinc1	11905	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:11247	disseminated intravascular coagulation Aliases: DIC Defibrination syndrome Diffuse or disseminated intravascular coagulation	Adamts13 Elane F13a1 F2 F3 Fga Gp6 Il10 Plat Proc Serpinc1 Tfpi Thbd Tnf	11905 14061 14066 14161 16153 18791 19123 21788 21824 21926 243816 279028 50701 74145	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10159	osteonecrosis Aliases: Avascular necrosis of bone aseptic necrosis bone necrosis	A2m Abcb1a Abcb1b Col2a1 F2 F5 Il23r Lrp5 Nos3 Plat Plg Proc Serpinc1 Tfpi Trpv4 Vwf	11905 12824 14061 14067 16973 18127 18669 18671 18791 18815 19123 209590 21788 22371 232345 63873	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110916	hereditary spherocytosis type 1 Aliases: HS1 SPH1 hereditary spherocytosis 1	ADD2 ANK1 EPB42 SPTA1	119 2038 286 6708	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070340	classic citrullinemia	Ass1	11898	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9273	citrullinemia Aliases: ASS deficiency deficiency of citrulline-aspartate ligase	Ass1 Slc25a13	11898 50799	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111527	spinal muscular atrophy with progressive myoclonic epilepsy Aliases: Jankovic-Rivera syndrome SMA-PME SMAPME hereditary myoclonus-progressive distal muscular atrophy syndrome	Asah1	11886	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1927	sphingolipidosis Aliases: sphingolipidoses	Asah1	11886	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050464	Farber lipogranulomatosis Aliases: Farber disease N-laurylsphingosine deacylase deficiency acid ceramidase deficiency	Asah1	11886	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10581	metachromatic leukodystrophy Aliases: MLD Scholz cerebral sclerosis arylsulfatase A deficiency deficiency of cerebroside-sulfatase sulfatide lipoidosis	Arsa Psap	11883 19156	Mus musculus (house mouse)	Alliance of Genome Resources

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