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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 **1026 - 1050** of **4649** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▼
DOID:2339	Crouzon syndrome Aliases: Craniofacial Dysostosis	FGFR2	2263	Homo sapiens (human)	Alliance of Genome Resources
DOID:2326	gastroenteritis Aliases: cholera morbus infectious colitis, enteritis and gastroenteritis	LALBA TGFA	3906 7039	Homo sapiens (human)	Alliance of Genome Resources
DOID:2320	obstructive lung disease Aliases: respiratory airway obstruction	A2M MMP1	2 4312	Homo sapiens (human)	Alliance of Genome Resources
DOID:2316	brain ischemia Aliases: Ischaemic encephalopathy Ischemic encephalopathy cerebral ischemia	ABCB1 ADAMTS1 AGER AKAP12 AKAP1 AKT1 ALOX15 ALOX5 ANGPT1 ANGPT2 ANXA1 APEX1 AQP3 AQP4 AQP5 AQP8 BAD BMP6 BTG2 C3 CASP6 CAST CAT CCL2 CCR5 CDK5 CLU CP CREB1 CSF2RB CSF3 CSPG4 CTSB CTSC CTSL CTSV DBH DPYSL2 DRD2 EDN1 EPOR F2R FAS FASLG FGA GAL GC GFRA1 GLUD1 GLUD2 HIF1A HSPA1B HSPA8 HSPA9 IL17A IL6ST IRAK1 IRAK4 ITGAM KCNK10 KCNK2 KDR LGALS3 LIF LONP1 MAP2 MAPT MDH2 MDK MMP13 MMP14 MMP2 MMP9 MSI1 NES NOS1 NOS3 NPPA NPTXR NR3C1 OPRM1 PAK1 PCNA PGF PLA2G4A PLAT PPP1R15A PRKACB PRKCA PROZ PTGIS PTGS1 PTGS2 RET SCN5A SELE SERPINE1 SLC11A2 SLC29A1 SLC6A1 SLC8A1 SLC8A2 SLC8A3 SOS1 SRC TEK TGFB1 TJP1 TLR4 TNFRSF1A TTR	1020 1075 10763 1191 1234 1356 1385 1439 1440 1464 1508 1514 1515 1621 177 1808 1813 1906 2030 2057 207 2149 2243 23467 23645 240 246 2638 2674 2746 2747 284 285 2908 301 3091 328 3304 3312 3313 343 355 356 3572 360 3605 361 362 3654 3684 3776 3791 3958 3976 4133 4137 4191 4192 4313 4318 4322 4323 4440 4842 4846 4878 4891 4988 5054 5058 51083 5111 51135 5228 5243 5321 5327 54207 5567 5578 572 5740 5742 5743 5979 6331 6347 6401 6529 654 6543 6546 6547 6654 6714 7010 7040 7082 7099 7132 718 7276 7832 8165 831 839 847 8858 9361 9510 9590	Homo sapiens (human)	Alliance of Genome Resources
DOID:231	motor neuron disease	DCTN1 KIF5B NOS1 SOD1 TARDBP VAPA VAPB VWA1	1639 23435 3799 4842 64856 6647 9217 9218	Homo sapiens (human)	Alliance of Genome Resources
DOID:2300	spondylolysis	SLC26A2	1836	Homo sapiens (human)	Alliance of Genome Resources
DOID:2297	leptospirosis Aliases: Fort Bragg fever Leptospirosis icterohaemorrhagica Rat Catcher's Yellows Weil's disease nanukayami fever spirochetal jaundice	ACHE BCHE F2 MBL2	2147 4153 43 590	Homo sapiens (human)	Alliance of Genome Resources
DOID:2280	hidradenitis suppurativa Aliases: Acne inversa, familial	CD163 LCN2 NCSTN TNF	23385 3934 7124 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:2277	gonadal disease	LHCGR	3973	Homo sapiens (human)	Alliance of Genome Resources
DOID:2272	vulvovaginal candidiasis Aliases: Candidal cervix Candidal vulvovaginitis Candidiasis of vulva and vagina Monilial vulvovaginitis	MBL2	4153	Homo sapiens (human)	Alliance of Genome Resources
DOID:2256	osteochondrodysplasia Aliases: Cartilage Development disorder Congenital anomaly of cartilage Osteochondrodysplasia syndrome chondrodystrophy skeletal dysplasia	ATF2 BMPR1B CEBPB CHST3 COL10A1 COL11A2 COL2A1 COL9A1 COL9A2 COL9A3 COMP DYM FLNA FLNB GOLGB1 HSPG2 LIFR MATN3 NPPC PTH1R RNF146 RYR1 SLC26A2 TGFB1 TGFB2 TGFBR1 TRPS1	1051 1280 1297 1298 1299 1300 1302 1311 1386 1836 2316 2317 2804 3339 3977 4148 4880 54808 5745 6261 658 7040 7042 7046 7227 81847 9469	Homo sapiens (human)	Alliance of Genome Resources
DOID:225	syndrome	APOO CDC42 NSD1 NSD2 NSD3 SCAF4 SCAF8 SVIP ZDHHC15	158866 22828 258010 54904 57466 64324 7468 79135 998	Homo sapiens (human)	Alliance of Genome Resources
DOID:2247	spondylosis Aliases: Lumbar spondylosis with myelopathy Spondylogenic compression of lumbar spinal cord Spondylogenic compression of thoracic spinal cord Thoracic or lumbar spondylosis with myelopathy lumbosacral spondylosis without myelopathy spondylosis with myelopathy	KL	9365	Homo sapiens (human)	Alliance of Genome Resources
DOID:224	transient cerebral ischemia Aliases: TIA TIA - Transient ischaemic attack Transient cerebral ischaemia Transient ischemic attacks transient ischemic attack	ACVRL1 ADAMTS1 ADAMTS4 AGER AGT AHR AIFM1 ANK1 ANK2 APOE AQP4 ATF2 ATP5F1B BACE1 BAX C3 CAMK2A CASP7 CASP9 CBL CCL2 CCNH CCR6 CDK5 CHKA CREB1 CSF3 CX3CL1 DAXX DBN1 DLL4 DUSP16 EIF2S1 ELANE ELK1 ENTPD1 EP300 EPO ERCC6 ESR1 F11R F12 FADD FAS FGFR1 FGFR2 FMR1 FTO G6PD GAD1 GAD2 GHSR GLRX GLUL GOT1 GPX3 GRIN2A GRIN2B H2AX HAVCR2 HIF1A HNRNPA2B1 HNRNPAB HRH2 HSF1 HSPA5 HSPA8 HSPB1 HTT ICAM1 IFNB1 IKBKB IL10 IL1RN ITGAM ITGB3 ITPR1 JAK1 KCNK2 KDM1A KLF5 KMT2A LCN2 LMNA LPAR1 LTBP1 MADD MAP2K4 MBD3 MBP MCFD2 MDM2 MECP2 MFF MMP2 MMP9 MT1E MT1H MT2A MTOR NAMPT NEFH NEFL NEFM NF1 NFKB1 NGFR NOS1 NOS3 NOTCH1 NOX1 NRG1 NRP1 NRXN1 OGG1 OPA1 OPTN PARP1 PAWR PCNA PLAT PLAU PLXND1 PPARG PPP1R15A PPP1R9A PTAFR PTEN PTGER4 PTGIS PTPN13 RACK1 ROBO1 ROBO2 RPS6 SEMA3E SERPINE1 SERPINF1 SIN3A SIRT6 SLC12A2 SLC17A6 SLC17A8 SLIT2 SMPD3 SOD1 SOD2 STAT3 TERT TFPI TIAL1 TNF TNFRSF1A TRPC6 UCP2 VWF WNK1 WNK2 XRCC1	10133 10135 1020 10399 1119 1235 1385 1386 142 1440 1616 1627 177 183 1902 196 1965 1991 2002 2033 2056 2074 2099 2161 2260 2263 23028 23129 2332 23621 23645 246213 2475 2539 2571 2572 25942 2693 27035 2745 2752 2805 286 287 2878 2903 2904 3014 3064 3084 3091 3181 3182 3274 3297 3309 3312 3315 3383 3456 348 355 3551 3557 3586 361 3684 3690 3708 3716 3776 3934 4000 4052 4155 4193 4204 4297 4313 4318 4493 4496 4502 4741 4744 4747 4763 4790 4804 4842 4846 4851 4968 4976 5054 506 5074 50848 5111 51548 5176 5327 5328 53615 54567 5468 55512 55607 56947 57084 5724 5728 5734 5740 5783 581 6091 6092 6194 6347 6376 6416 65125 65268 6558 6647 6648 6774 688 7015 7035 7073 7124 7132 718 7225 7351 7450 7515 79068 80824 815 840 842 84868 8567 867 8772 8829 902 90411 9131 9353 9378 94 9507 9510 953 9723	Homo sapiens (human)	Alliance of Genome Resources
DOID:2237	hepatitis Aliases: acute and subacute liver necrosis acute hepatitis acute/subac. necrosis of liver animal hepatitis chronic hepatitis chronic persistent hepatitis	ABO AFP ATP7B F5 GOLM1 IFNG LIPC NOS2 OGG1 PDCD1 SPP1 TF	174 2153 28 3458 3990 4843 4968 51280 5133 540 6696 7018	Homo sapiens (human)	Alliance of Genome Resources
DOID:2236	congenital afibrinogenemia Aliases: Factor I deficiency Fibrinogen deficiency	FGA FGB FGG	2243 2244 2266	Homo sapiens (human)	Alliance of Genome Resources
DOID:2235	prothrombin deficiency Aliases: Congenital factor II deficiency Hereditary factor II deficiency disease hypoprothrombinemia	F2 F7	2147 2155	Homo sapiens (human)	Alliance of Genome Resources
DOID:2234	focal epilepsy Aliases: localisation-related epilepsy partial epilepsy	CNR1 DEPDC5 MMP9	1268 4318 9681	Homo sapiens (human)	Alliance of Genome Resources
DOID:2231	factor XII deficiency Aliases: Factor XII deficiency disease Hageman Factor deficiency deficiency, Hageman	F12	2161	Homo sapiens (human)	Alliance of Genome Resources
DOID:2229	factor XI deficiency Aliases: Congenital factor XI deficiency Hereditary factor XI deficiency disease Rosenthal's disease hemophilia C plasma thromboplastin antecedent deficiency	F11	2160	Homo sapiens (human)	Alliance of Genome Resources
DOID:2228	thrombocytosis Aliases: Thrombocythaemia	CALR CPB2 MPL THPO	1361 4352 7066 811	Homo sapiens (human)	Alliance of Genome Resources
DOID:2226	myeloproliferative neoplasm Aliases: CMPD CMPD, U chronic myeloproliferative disease	ASXL1 CBL CSF3R PDGFRB TET2	1441 171023 5159 54790 867	Homo sapiens (human)	Alliance of Genome Resources
DOID:2224	essential thrombocythemia Aliases: Essential thrombocythaemia familial thrombocytosis hemorrhagic thrombocythemia hereditary thrombocythemia primary Thrombocytosis	CALR CD36 CD40LG ELANE MPL THPO VCAM1 VWF	1991 4352 7066 7412 7450 811 948 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:2223	platelet storage pool deficiency Aliases: Dense body defect Platelet dense granule deficiency Platelet storage pool defect	AP3B1 DOCK7 DTNBP1 LYST SLC7A11	1130 23657 84062 85440 8546	Homo sapiens (human)	Alliance of Genome Resources
DOID:2222	factor X deficiency Aliases: disease, Stuart-Prower	F10	2159	Homo sapiens (human)	Alliance of Genome Resources

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