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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 **11401 - 11425** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism ▼	Source
DOID:649	prion disease Aliases: Prion disease pathway Prion protein disease Spongiform Encephalopathy prion induced disorder transmissible spongiform encephalopathy	CX3CL1 SOD1 USP14	6376 6647 9097	Homo sapiens (human)	Alliance of Genome Resources
DOID:11729	Lyme disease Aliases: Bannwarth syndrome Bannworth's syndrome Lyme borreliosis Neurological Lyme disease lyme neuroborreliosis neuroborreliosis	PLAUR	5329	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111758	Y-linked deafness 2 Aliases: DFNY2	TBL1Y	90665	Homo sapiens (human)	Alliance of Genome Resources
DOID:684	hepatocellular carcinoma Aliases: Hepatoma	A2M ABCA1 ABCB1 ABCB4 ABCC3 ABCE1 ACE ACER3 ADIPOQ AFP AK3 AKR1B1 AKT1 AKT2 ALB ALDH2 ALDH7A1 ALDOC ALX4 ANXA2 ANXA6 APC APEX1 APOA1 APOA2 APOA4 APOC2 APOC3 APOC4 APRT ARID1A ARID2 ASPM ASS1 ATP7B AZGP1 BAX BCORL1 BMI1 C3 CA12 CA9 CAD CADM1 CADM2 CALR CAPN3 CASP9 CAT CBFB CBL CBX2 CBX4 CCL2 CCL5 CD274 CD68 CDH1 CDK12 CDK13 CEBPB CEP164 CES1 CHD4 CHD5 CKAP4 CLDN1 CLPTM1L COL18A1 COX1 CPS1 CSF1R CTLA4 CTNNB1 CTSB CTSL CTSV CUX1 CXCR4 CYP2C19 CYP2E1 DDR1 DDR2 DDX3X DICER1 DNMT1 DSN1 EFEMP1 EFTUD2 EGF EGFR ENAH ENG EP300 EPCAM EPO ERBB3 ERBB4 ERN1 EZH2 F2 FAS FASLG FGFR1 FGFR2 FGFR4 FLT3 FOSL2 FOXA1 FOXM1 FOXO1 FOXP1 FTH1 FUBP1 G6PC1 G6PD GC GGT1 GMPS GNMT GOLM1 GPC1 GPC3 GPX1 GPX3 GRB7 HAVCR1 HAVCR2 HDAC2 HDAC4 HFE HIF1A HILPDA HLA-DPA1 HLA-DQA1 HLA-DQB1 HMGCS2 HNF1A HNRNPA1 HNRNPA2B1 HNRNPAB HNRNPD HNRNPH1 HP HPRT1 HRAS ICAM1 IDH2 IFNA2 IFNL1 IGF1R IGF2 IGF2R IKZF1 IL10 IL12A IL15RA IL18R1 IL21 IL2 IL6 IL6ST ING3 INSR IQGAP2 ITIH4 JAG1 JAK1 JUND KAT2B KCNH1 KDM1A KDM3A KDM6A KDR KIF1B KIR3DS1 KLF4 KLRF1 KMT2B KRAS KRT18 LEP LEPR LPAR1 LRP1B MAP2K2 MAP2K4 MAP3K1 MAP4K4 MBL2 MCM7 MDM2 MECP2 MET MME MPO MTDH MTOR MYC MYD88 ND5 NEIL3 NFE2L1 NFE2L2 NFKB1 NLRC5 NOS2 NRAS NRG1 NRP1 NUF2 PAFAH1B1 PCNA PDCD1 PDGFRL PFAS PHF6 PIK3CA PIK3CB PIK3R3 PINX1 PLAU PLCG1 PLOD3 PNPLA3 PON1 PPARA PPARG PPAT PPP1R9A PPP1R9B PRDM1 PREX2 PRL PTCH1 PTEN PTGS2 PTK2 PTPN13 PTPRB RAC1 RB1 RBM10 RECQL RGN RICTOR RNF43 RUNX1 RUNX3 RYR3 SARDH SERPINB5 SERPINF1 SF3B1 SF3B4 SHC1 SIX1 SKP2 SLC38A1 SLC7A5 SLCO1B3 SMAD4 SMARCA4 SMARCB1 SMARCC1 SMC3 SMG9 SMO SNRPE SNW1 SOAT2 SOD2 SOX30 SPAG9 SPOCK1 SPOP SPP1 SRC SRF STAT4 STAT5B STC2 STIM1 STMN1 TBX3 TEK TEP1 TERT TET1 TET2 TFRC TGFA TGFBR2 TLR2 TLR3 TLR4 TLR9 TNF TNFAIP3 TP53 TRAF7 TSC2 TTK TTR TYMS UACA VAV1 VEGFA VEGFC WNT2 XPO1 XPO5 XRCC1 YWHAZ ZFHX3	10262 10320 1051 1066 10788 10970 11063 1108 1373 1436 1493 1499 1508 1514 1515 1523 1557 1571 1636 1654 174 1757 1786 182 19 1902 1950 1956 196528 2 2022 2033 2056 2065 2066 207 208 2081 213 2146 2147 217 2202 2260 2263 2264 22897 22938 230 23028 2305 2308 23095 231 2322 23405 23451 2355 23705 2475 2495 253260 253559 2538 2539 259266 26038 2638 26762 2678 27086 2719 27232 2817 28234 282618 2876 2878 2886 29126 29923 302 3066 3077 3084 309 3091 3113 3117 3119 3158 3169 3178 3181 3182 3184 3187 324 3240 3251 3265 328 335 336 337 3383 3418 344 3440 345 346 3480 3481 3482 353 355 3558 356 3569 3572 3586 3592 3601 3643 3700 3716 3727 3756 3791 3813 3845 3875 3925 3952 3953 4072 4089 4153 4176 4193 4204 4214 4233 4311 4353 445 4512 4540 4609 4615 463 4779 4780 4790 4843 4893 4921 501 5048 50808 5111 51280 5133 51348 5157 51755 5176 5198 5243 5244 5268 5290 5291 5328 5335 53353 540 54106 5444 54556 5465 5468 5471 54790 54894 54984 55075 55247 55331 55607 55740 55818 56006 5605 5617 563 5727 5728 5743 5747 57510 5783 5787 581 5879 59067 5925 5965 60529 6059 6263 63035 6347 6352 639 6416 6464 648 6495 6502 6597 6598 6599 6608 6635 6648 6695 6696 6714 6722 6775 6777 6786 6926 6927 7010 7011 7015 7037 7039 7048 7097 7098 7099 7124 7128 7157 718 7249 7272 7276 7298 7403 7409 7422 7424 7472 7514 7515 7534 768 771 780 7852 790 79980 80243 80312 80339 80781 81037 811 8140 81539 8241 825 8289 83540 8405 84166 842 84231 84295 8435 84687 847 84733 84868 8503 8535 861 8614 8621 864 865 867 8714 8809 8829 8833 8850 8880 8985 9043 9076 9104 9126 92140 9314 9343 9370 9448 968 9757 9759 999	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060614	ulnar-mammary syndrome Aliases: Pallister ulnar-mammary syndrome Schinzel syndrome	TBX3	6926	Homo sapiens (human)	Alliance of Genome Resources
DOID:646	viral encephalitis Aliases: epidemic encephalitis	E2F1 MMP9	1869 4318	Homo sapiens (human)	Alliance of Genome Resources
DOID:11121	pulpitis Aliases: pulp stones	IFNG IL1R1 TLR4	3458 3554 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:10873	Kuhnt-Junius degeneration Aliases: Exudative senile macular degeneration of retina Neovascular age-related macular degeneration Senile macular degeneration, wet Wet senile macular retinal degeneration	ANXA5 APOE C3 CCL2 CCR2 CFI ELN FLT1 IGF1R IGFBP2 IL6 KDR LOXL1 NOS3 PDGFB PDGFRB PON1 SOD2 TLR2 TLR3 VEGFA	2006 2321 308 3426 348 3480 3485 3569 3791 4016 4846 5155 5159 5444 6347 6648 7097 7098 718 729230 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:10914	amnestic disorder Aliases: Amnestic syndrome Korsakoff's psychosis or syndrome amnesia	BCHE BDNF CREB1 DRD3 HRH3 HTR7 IRS1 IRS2 IRS4 MAPT	11255 1385 1814 3363 3667 4137 590 627 8471 8660	Homo sapiens (human)	Alliance of Genome Resources
DOID:8283	peritonitis Aliases: Retractile mesenteritis acute generalized peritonitis primary bacterial peritonitis sclerosing mesenteritis	A2M ALDOB ESR1 FOXP1 GUSB IL6 NPPA PLAT PLAU TNF	2 2099 229 27086 2990 3569 4878 5327 5328 7124	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110424	dilated cardiomyopathy 1CC Aliases: CMD1CC	NEXN	91624	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:0070138	autosomal recessive cutis laxa type IIIB Aliases: ARCL3B De Barsy syndrome B	PYCR1	5831	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080403	orofacial cleft 10 Aliases: nonsyndromic cleft lip with or without cleft palate 10	SUMO1	7341	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080239	autosomal recessive intellectual developmental disorder 61 Aliases: Alwadei syndrome autosomal recessive intellectual developmental disorder-61 autosomal recessive mental retardation 61	RUSC2	9853	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111292	idiopathic generalized epilepsy 10 Aliases: EIG10	GABRD	2563	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112021	non-syndromic X-linked intellectual disability ARX-related Aliases: ARX-related intellectual disability MRXARX X-linked mental retardation 29 X-linked mental retardation 29 and others X-linked mental retardation 32 X-linked mental retardation 33 X-linked mental retardation 38 X-linked mental retardation 43 X-linked mental retardation 52 X-linked mental retardation 54 X-linked mental retardation 76 X-linked mental retardation 87 X-linked mental retardation with or without seizures ARX-related	ARX	170302	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080984	X-linked intellectual developmental disorder 109 Aliases: Fragile XE syndrome fragile site on chromosome Xq28	AFF2	2334	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070346	neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies	INTS1	26173	Homo sapiens (human)	Alliance of Genome Resources
DOID:13608	biliary atresia Aliases: Atresia of bile duct Congenital biliary atresia biliary atresia, congenital	ADD3 ADIPOQ CD14 DLK1 GGT1 GLI2 ICAM1 PTEN SHH SPINT1 SPINT2 SPP1 TGFB1	10653 120 2678 2736 3383 5728 6469 6692 6696 7040 8788 929 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050736	autosomal dominant disease	FGFR3	2261	Homo sapiens (human)	Alliance of Genome Resources
DOID:5113	nutritional deficiency disease	SOD1	6647	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081319	multiple synostoses syndrome 3	FGF9	2254	Homo sapiens (human)	Alliance of Genome Resources
DOID:8481	rheumatic myocarditis Aliases: Rheumatic degeneration of myocardium Rheumatic fever with myocarditis Rheumatoid myocarditis active rheumatic fever with myocarditis acute rheumatic carditis acute rheumatic myocarditis	GSN ICAM1 SELE VCAM1	2934 3383 6401 7412	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081361	spastic quadriplegic cerebral palsy 3 Aliases: CPSQ3	ADD1 ADD2 ADD3	118 119 120	Homo sapiens (human)	Alliance of Genome Resources

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