GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

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	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **76 - 100** of **4115** in total

« First

‹ Prev

1

2

3

4

5

6

7

8

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0080208	metabolic dysfunction-associated steatotic liver disease Aliases: MAFLD MASLD NAFLD metabolic dysfunction-associated fatty liver disease metabolic dysfunction-related steatotic liver disease metabolic-associated fatty liver disease non-alcoholic fatty liver disease nonalcoholic fatty liver disease	ABCC2 ADIPOQ ADRB3 AKT1 ALDH2 CCR2 DGAT2 HFE IL6 LEPR PNPLA3 PPARGC1A SAMM50 SOD2 TG	10891 1244 155 207 217 25813 3077 3569 3953 6648 7038 729230 80339 84649 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:4947	cholangiocarcinoma Aliases: adult primary Cholangiocarcinoma adult primary cholangiocellular carcinoma cholangiosarcoma	ABCC2 ALB APC ASPH EZH2 FASLG GNAS MGMT NAT2 OGG1 PPIA PREX2 RNF43 SLC7A5 THBS1 WDHD1	10 11169 1244 213 2146 2778 324 356 4255 444 4968 5478 54894 7057 80243 8140	Homo sapiens (human)	Alliance of Genome Resources
DOID:2741	bilirubin metabolic disorder Aliases: hereditary hyperbilirubinemia hyperbilirubinemia	ABCC2 HGF SLCO1B1 SLCO1B3 SOD2 UGT1A1	10599 1244 28234 3082 54658 6648	Homo sapiens (human)	Alliance of Genome Resources
DOID:12308	Dubin-Johnson syndrome Aliases: Dubin Johnson syndrome chronic idiopathic jaundice	ABCC2	1244	Homo sapiens (human)	Alliance of Genome Resources
DOID:2044	drug-induced hepatitis Aliases: Drug-induced chronic hepatitis	ABCC2	1244	Homo sapiens (human)	Alliance of Genome Resources
DOID:2738	pseudoxanthoma elasticum Aliases: Gronblad-Strandberg syndrome	ABCC6 CAT ELN GPX1 MMP2 SOD2 VEGFA XYLT1 XYLT2	2006 2876 368 4313 64131 64132 6648 7422 847	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050644	arterial calcification of infancy Aliases: generalized arterial calcification of infancy idiopathic infantile arterial calcification infantile arteriosclerosis	ABCC6 ENPP1	368 5167	Homo sapiens (human)	Alliance of Genome Resources
DOID:10763	hypertension Aliases: HTN hyperpiesia vascular hypertensive disorder	ABCC8 ABO ACE2 ACE ADD1 ADD2 ADRA1A ADRB1 ADRB2 ADRB3 AGT AGTR1 ALDH2 ANGPT1 ATP1A2 AVPR1A BDKRB1 BDKRB2 BRCA1 CACNB2 CCR5 CD14 CHGA CLCNKB CLU COL6A3 COMT CORIN CYP11B2 CYP2C9 CYP2J2 CYP2R1 CYP4A11 DBH DRD1 DRD2 ECE1 EDN1 EDN2 EDNRA EPHX2 F11R F7 FTO GCK GLCE GNAS GPX3 HGF HLA-DQA1 HP HSD11B1 HSD11B2 HSD3B1 HTR2A IL1RN IL6 INPPL1 INVS ITGA9 KCNMB1 KDR KLK1 LEP LEPR LOX LPL MMP1 MMP2 MMP9 MOV10 MTR NOS2 NOS3 NPHP3 NPPB NPPC NPR3 OGG1 PON1 PPARG PRLHR PTGIS PTPRD RAMP2 REN SLC6A2 SLC8A1 SOD1 SOD2 TNF TRHR UCP2 VEGFA WNK1 XRCC1	10266 10699 1113 118 1188 119 1191 120227 1234 1293 1312 148 153 154 155 1559 1573 1579 1585 1621 1636 1812 1813 183 185 1889 1906 1907 1909 2053 2155 217 26035 2645 27031 27130 2778 28 2834 284 2878 3082 3117 3240 3283 3290 3291 3356 3557 3569 3636 3680 3779 3791 3816 3952 3953 4015 4023 4312 4313 4318 4343 4548 477 4843 4846 4879 4880 4883 4968 50848 5444 5468 552 5740 5789 59272 5972 623 624 65125 6530 6546 6647 6648 672 6833 7124 7201 7351 7422 7515 783 79068 929	Homo sapiens (human)	Alliance of Genome Resources
DOID:2018	hyperinsulinism Aliases: hyperinsulinemia	ABCC8 AGT GCK GLUD1 IL6 INS KCNJ11 LTA PTPRF	183 2645 2746 3569 3630 3767 4049 5792 6833	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060639	permanent neonatal diabetes mellitus Aliases: PDMI PNDM permanent diabetes mellitus of infancy	ABCC8 GCK INS KCNJ11	2645 3630 3767 6833	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112262	leucine-sensitive hypoglycemia of infancy Aliases: LIH leucine-induced hypoglycemia	ABCC8	6833	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070219	familial hyperinsulinemic hypoglycemia 1 Aliases: HHF1	ABCC8	6833	Homo sapiens (human)	Alliance of Genome Resources
DOID:12930	dilated cardiomyopathy Aliases: primary dilated cardiomyopathy	ABCC9 ACTC1 APOE CAP2 CDK8 CS DES DMD DSG2 DSP EMD EYA4 FKRP GPX1 HFE HLA-DQB1 LDB3 LEPR LMNA MEF2A MMP1 MYH7 NEBL NFATC4 PRKCA RBM20 RBPJ SOD2 SP4 TNNI3 TTN VCL VEZF1	10060 1024 10486 10529 11155 1431 1674 1756 1829 1832 2010 2070 282996 2876 3077 3119 348 3516 3953 4000 4205 4312 4625 4776 5578 6648 6671 70 7137 7273 7414 7716 79147	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050650	familial atrial fibrillation Aliases: ATFB	ABCC9 KCNE2 KCNQ1 NPPA NUP155 SCN1B SCN2B SCN5A ZFHX3	10060 3784 463 4878 6324 6327 6331 9631 9992	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type Aliases: Cantu syndrome	ABCC9	10060	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110451	dilated cardiomyopathy 1O Aliases: CMD1O dilated cardiomyopathy with ventricular tachycardia	ABCC9	10060	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070600	intellectual disability and myopathy syndrome Aliases: ABCC9-related intellectual disability and myopathy AIMS IDMYS	ABCC9	10060	Homo sapiens (human)	Alliance of Genome Resources
DOID:10588	adrenoleukodystrophy Aliases: ALD Bronze Schilder disease Encephalitis periaxialis concentrica Encephalitis periaxialis, Schilder's Siemerling-Creutzfeldt Disease X-linked adrenoleukodystrophy diffuse sclerosis sudanophilic cerebral sclerosis	ABCD1	215	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111066	congenital bile acid synthesis defect 5 Aliases: CBAS5	ABCD3	5825	Homo sapiens (human)	Alliance of Genome Resources
DOID:905	Zellweger syndrome Aliases: cerebrohepatorenal syndrome congenital iron overload	ABCD3	5825	Homo sapiens (human)	Alliance of Genome Resources
DOID:9538	multiple myeloma Aliases: myeloma	ABCG2 ACE APOE CD40 CD40LG CFHR1 CTLA4 CYP1A1 CYP2C19 FCGR2A FGG GPX1 GPX3 HFE HK1 ICAM1 IL10 IL1A IL1RN IL4R IRF4 KRAS MEFV MET MTR NRAS PON1 ROBO1 SOD2 SPARC SPP1 TFRC TGFB1 TNF TNFRSF10A TNFRSF17 TP53 TYMS VEGFA XPO5 XRCC5	1493 1543 1557 1636 2212 2266 2876 2878 3077 3078 3098 3383 348 3552 3557 3566 3586 3662 3845 4210 4233 4548 4893 5444 57510 608 6091 6648 6678 6696 7037 7040 7124 7157 7298 7422 7520 8797 9429 958 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:13189	gout Aliases: Articular gout Gouty arthropathy gouty arthritis	ABCG2 ADRB3 HP PRPS1 SLC17A3	10786 155 3240 5631 9429	Homo sapiens (human)	Alliance of Genome Resources
DOID:707	B-cell lymphoma Aliases: B-cell lymphocytic neoplasm	ABCG2 BRD2 BTK CD40 EZH2 IL21R	2146 50615 6046 695 9429 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:2349	arteriosclerosis Aliases: Arteriosclerotic vascular disease	ABCG5 ABCG8 AKR1B1 ALDH3A1 ALOX5 APOB ESR1 F13A1 HP HSPD1 IL10 IL6ST ITGA2 LCAT LDLR MMP12 MMP13 MMP1 MMP2 MMP3 MMP9 MSR1 PON1 PTGER4 PTGS2 SERPINA1 TLR4	2099 2162 218 231 240 3240 3329 338 3572 3586 3673 3931 3949 4312 4313 4314 4318 4321 4322 4481 5265 5444 5734 5743 64240 64241 7099	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090019	sitosterolemia 1 Aliases: phytosterolemia	ABCG5 ABCG8	64240 64241	Homo sapiens (human)	Alliance of Genome Resources

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Guidelines

International Collaboration

Acknowledgements