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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 **51 - 75** of **4649** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:13619	extrahepatic cholestasis Aliases: extrahepatic biliary Stasis extrahepatic obstructive biliary disease	ABCA1 ABCC4 CYP27A1 CYP7A1 CYP8B1 HMGCS2 HNF1A LGALS1 NFE2L2 OPRM1 PDGFRB SETD7 SLC22A1 SLC22A2	10257 1581 1582 1593 19 3158 3956 4780 4988 5159 6580 6582 6927 80854	Homo sapiens (human)	Alliance of Genome Resources
DOID:3393	coronary artery disease Aliases: CHD Coronary disease coronary arteriosclerosis coronary heart disease	ABCA1 ABCC6 ACAT2 ACE ADIPOQ ADRB3 AGER AGTR1 AHSG APOA1 APOA2 APOA5 APOB APOC3 APOE APOM ARHGAP31 BCHE BRINP3 BTNL2 C1orf167 CBS CCL2 CCR1 CCR2 CCR5 CD14 CD40LG CDH5 CHI3L1 CLCN6 CLU CPE CUBN CYP2R1 ECE1 EDN1 ENG EPHX2 ESR1 F2 F7 FCGR2A FCGR3A FGB FTO GCK GP6 GPX1 GPX3 HFE HGF HMGCR HNF1A HP HSD11B1 HSPD1 IL10 IL15 IL1RL1 IL6 IRS1 ITGA2 KALRN KL LDLR LEPR LIPC LIPG LOX LPA LPL LRP8 LTA LUM MAP3K7 MLXIPL MMP12 MMP1 MMP3 MMP9 MYLK NAMPT NGF NGFR NOD2 NOS2 NOS3 NPPA NR1H3 NR3C1 OGG1 OLR1 PAPPA PECAM1 PLA2G7 PNPLA3 PON1 PON2 PPARA PPARG PTPN1 PTPRD RBP4 SELE SERPINA1 SERPINE1 SERPINF2 SLC2A4 SOAT2 SOD1 SOD3 SPP1 SREBF1 SREBF2 TEK THBD TLL1 TLR4 TNF TNFRSF11B TNFRSF1A TNNI3 TP53 TTN VEGFA VIM VTN XRCC1	1003 10062 10135 1116 116519 1185 1191 120227 1230 1234 1363 155 1636 177 185 1889 19 1906 197 2022 2053 2099 2147 2155 2212 2214 2244 2645 284498 2876 2878 2908 3077 3082 3156 3240 3290 3329 335 336 338 339479 345 348 3569 3586 3600 3667 3673 368 39 3949 3953 3990 4015 4018 4023 4049 4060 4312 4314 4318 4321 4638 4803 4804 4843 4846 4878 4968 4973 4982 5054 5069 51085 51206 5175 5265 5345 5444 5445 5465 5468 55937 56244 57514 5770 5789 590 5950 6347 6401 64127 6517 6647 6649 6696 6720 6721 6885 6927 7010 7056 7092 7099 7124 7132 7137 7157 7273 729230 7422 7431 7448 7515 7804 79068 7941 8029 80339 8435 875 8997 9173 929 9365 9370 9388 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:1387	hypolipoproteinemia Aliases: Hypolipoproteinaemia	ABCA1 APOA1	19 335	Homo sapiens (human)	Alliance of Genome Resources
DOID:10230	aortic atherosclerosis Aliases: Atherosclerosis of aorta	ABCA1 APOE CAPN1 EDN1 LDLR	19 1906 348 3949 823	Homo sapiens (human)	Alliance of Genome Resources
DOID:10787	premature menopause Aliases: Menopause - premature Menopause praecox	ABCA1 HMGCR	19 3156	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080957	primary hypoalphalipoproteinemia 1 Aliases: familial HDL deficiency familial hypoalphalipoproteinemia	ABCA1	19	Homo sapiens (human)	Alliance of Genome Resources
DOID:1388	Tangier disease Aliases: familial alpha-lipoprotein deficiency familial high density lipoprotein deficiency	ABCA1	19	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060713	autosomal recessive congenital ichthyosis 4B Aliases: ARCI4B harlequin ichthyosis harlequin type ichthyosis congenita harlequin type ichthyosis fetalis	ABCA12 CST6 PIGA PRSS8	1474 26154 5277 5652	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060656	autosomal recessive congenital ichthyosis 1 Aliases: ARCI1	ABCA12	26154	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060712	autosomal recessive congenital ichthyosis 4A Aliases: ARCI4A ICR2B ichthyosis congenita IIB lamellar ichthyosis 2	ABCA12	26154	Homo sapiens (human)	Alliance of Genome Resources
DOID:3717	gastric adenocarcinoma Aliases: adenocarcinoma of stomach stomach adenocarcinoma	ABCA13 ALX4 AMIGO2 APOC3 ARID1A CAT CD44 CDK12 GPX1 HLA-DQA1 HNRNPA0 IL6 KMT2D MAP2K4 MAPK14 PLCE1 POLE PTPN13 PTPRA PTPRZ1 RAC1 RNASET2 RNF43 SLC7A5 STAT1 STAT5A STAT5B STAT6 TP53 UBR5 XPO1	10949 1432 154664 2876 3117 345 347902 3569 51196 51366 51755 5426 54894 5783 5786 5803 5879 60529 6416 6772 6776 6777 6778 7157 7514 8085 8140 8289 847 8635 960	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060041	autism spectrum disorder	ABCA3 ARHGAP32 ASH1L AVPR1B BAIAP2 BCL11A BDNF BORCS8-MEF2B BRINP1 CADM2 CAMK2A CASK CFL1 CHD1 CHD2 CHD6 CHD7 CHD8 CHD9 CHRNB2 CNTNAP1 CNTNAP2 CNTNAP3 CNTNAP3B CNTNAP4 CNTNAP5 COMT CREB1 CREBBP CSDE1 CTNNB1 CTNND1 CTNND2 CUL3 CYFIP1 DLGAP4 DSCAM DSCAML1 DYRK1A EIF4B EIF4E ELP2 EN2 EXT1 FMR1 FOXP2 FXR1 FXR2 GABRB3 GAD1 GAD2 GRIN1 HTR2A HTR2B HTR2C IHH ITGA4 ITPR3 KDM5B KMT5B KMT5C LAMC1 LAMC2 LAMC3 LRBA LRFN2 MAOA MBD5 MBD6 MEF2A MEF2B MEF2C MEF2D MET MMP9 MOCOS NAA15 NAA16 NBEA NDST1 NDST2 NDST3 NDST4 NLGN1 NLGN2 NLGN3 NLGN4X NLGN4Y NR3C2 NRCAM NRP2 NRXN1 NRXN2 NRXN3 OPRL1 OPRM1 PAK2 PDGFRB PIANP PKP2 PKP4 POGZ PREX1 PRICKLE1 PTEN RIMS1 RIMS2 SCAMP1 SCAMP2 SCN1A SCN2A SHANK1 SHANK2 SHH SLC25A12 SLC6A2 SLC6A3 SLC6A4 SLC7A5 SLC9A9 SRSF11 SSBP2 SSBP3 SSBP4 SYN1 SYN2 SYN3 SYNGAP1 TAOK1 TAOK2 TBR1 TCF20 TMPRSS9 TPH1 TRPC4 TRPC5 TSC1 TSC2 TSHZ3 UBE3A VRK3 WDFY3 WDR75 ZNF280B ZNF280D	100271849 10066 10319 10458 10716 1072 10765 1105 1106 1141 114785 129684 1312 1385 1387 140883 144165 1499 1500 1501 1620 170463 1826 1859 196500 1975 1977 2020 21 2131 22829 22839 22871 22941 22999 23001 23126 23191 2332 23635 23648 253559 2562 2571 2572 26047 26960 285195 2902 3340 3356 3357 3358 3549 360200 3676 3710 3915 3918 4128 4205 4207 4208 4209 4233 4306 4318 4897 4987 4988 5062 50944 51111 51231 5159 5318 53335 54413 54816 55034 55250 553 55636 55777 55870 5728 57453 57497 57502 57551 57555 57580 57616 57680 627 6323 6326 64579 6469 6530 6531 6532 6853 6854 6942 7166 7223 7224 7248 7249 728577 7337 7812 79612 79937 80155 80205 8087 8140 815 8224 84128 84181 8452 84787 8502 8506 8509 85445 8573 8604 8828 8831 9295 9344 9348 9369 9378 9379 93986 9513 9522 9699 9743 987	Homo sapiens (human)	Alliance of Genome Resources
DOID:12120	pulmonary alveolar proteinosis	ABCA3 CSF2 CSF2RA CSF2RB DEFB1 MARS1 SFTPA1 SFTPB SFTPC SFTPD	1437 1438 1439 1672 21 4141 6439 6440 6441 653509	Homo sapiens (human)	Alliance of Genome Resources
DOID:10584	retinitis pigmentosa Aliases: pericentral pigmentary retinopathy	ABCA4 ADGRV1 AIFM1 BCAN CA4 CAT CC2D2A CLRN1 CNGA1 CNGB1 CRB1 CRB2 CWC27 EDN1 EPG5 EYS FDXR FGFR2 GRIN2B GUCY2D HGF HK1 HKDC1 IMPG1 KL MFRP MT1E MT1H MT2A NGF PDE6B POC5 POMGNT1 PRPF3 PRPF4 PRPF8 PRPH2 PRPS1 PTEN RGR RHO RLBP1 SERPINF1 SLC6A6 SNRNP200 SOD1 USH2A VEGFA	10283 10594 1258 1259 134359 1906 2232 2263 23020 23418 24 286204 2904 3000 3082 3098 346007 3617 4493 4496 4502 4803 5158 5176 55624 5631 5728 57545 57724 5961 5995 6010 6017 63827 6533 6647 7399 7401 7422 762 80201 83552 84059 847 9128 9129 9131 9365	Homo sapiens (human)	Alliance of Genome Resources
DOID:4448	macular degeneration Aliases: Macular degeneration of retina	ABCA4 APOE BAD BAX BMP4 C2 C3 CCL2 CCR2 CD36 CDKN1B CFB CFH CFI CRYAB EFEMP1 ELN ERCC6 ESR1 FAS HSPA8 IL17A KDR MMP2 MMP9 NFE2L2 PON1 PPARGC1A PRPH2 SERPINE1 SERPINF1 SERPING1 SIRT1 SOD1 SRSF10 TLR4 TRA2B	1027 10772 10891 1410 2006 2074 2099 2202 23411 24 3075 3312 3426 348 355 3605 3791 4313 4318 4780 5054 5176 5444 572 581 5961 629 6347 6434 652 6647 7099 710 717 718 729230 948	Homo sapiens (human)	Alliance of Genome Resources
DOID:8466	retinal degeneration Aliases: degeneration of retina	ABCA4 BARD1 BAX BDNF C3 CARD9 CFB CFH CLU CS DMD EYS FCGR1A HDAC4 HGF INHBA KCNH8 LCN2 MERTK NOS3 OTX1 OTX2 PARK7 PDE6B PDHA1 PDHA2 PKD2 PLCB4 PROM1 PROM2 PRPH2 PTPRC RAB6A SERPINF1 SH3RF1 TFPI2 VDAC1 VDAC2 VDAC3	10461 11315 1191 131096 1431 150696 1756 2209 24 3075 3082 346007 3624 3934 4846 5013 5015 5158 5160 5161 5176 5311 5332 57630 5788 580 581 5870 5961 627 629 64170 718 7416 7417 7419 7980 8842 9759	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050817	Stargardt disease Aliases: STARGARDT DISEASE 1	ABCA4 ELOVL4	24 6785	Homo sapiens (human)	Alliance of Genome Resources
DOID:8501	fundus dystrophy Aliases: Retinal Dystrophy	ABCA4 PRPH2	24 5961	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111013	cone-rod dystrophy 3 Aliases: CORD3	ABCA4	24	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110354	retinitis pigmentosa 19 Aliases: RP19	ABCA4	24	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110015	age related macular degeneration 2 Aliases: ARMD2	ABCA4	24	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111364	Alzheimer's disease 9 Aliases: AD9 Alzheimer's disease 9, late onset	ABCA7	10347	Homo sapiens (human)	Alliance of Genome Resources
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	ABCB1 ABCC2 ABCC3 ABCG5 ABCG8 ACACA ACACB ACADM ACADVL ACO1 ACTB ADAMTS13 ADIPOQ ADRB3 AHCY AKT1 ALDH2 APOE ATP5F1A AZGP1 CCL2 CCL5 CCR2 CD163 COL1A1 CYP2E1 DGAT2 EZH2 FASN FOXO1 FTO G6PD GPAM HADHA HFE HMGCR HP HPR IFNA2 IGF1R IGFBP7 IL10 IL13 IL1RN IL6 INSR IRS1 IRS2 KRT18 LEP LEPR LPL MLXIPL MLYCD NAMPT NFE2L2 PKLR PLA2G7 PLIN1 PLIN2 PLIN3 PLIN5 PNPLA3 PON2 PPARGC1A PPARGC1B PPDPF RARRES2 SAMM50 SCD SERPINE1 SIDT2 SIRT1 SIRT2 SIRT3 SIRT4 SIRT6 SLC7A3 SOD2 SREBF1 STAT3 TFRC TG TLR4 TLR9 TNF UBR1 UCP2	10135 10226 10891 11093 123 1244 1277 133522 155 1571 191 197131 207 2146 217 2194 22933 2308 23409 23410 23411 23417 2539 25813 3030 3077 31 3156 32 3240 3250 34 3440 348 3480 3490 3557 3569 3586 3596 3643 3667 37 3875 3952 3953 4023 440503 4780 48 498 5054 51085 51092 51548 5243 5313 5346 54106 5445 563 57678 5919 60 6319 6347 6352 64240 64241 6648 6720 6774 7037 7038 7099 7124 729230 7351 79068 79144 7941 80339 84649 84889 8660 8714 9332 9370	Homo sapiens (human)	Alliance of Genome Resources
DOID:8552	chronic myeloid leukemia Aliases: CML CML - chronic Myelogenous Leukemia Myeloid Leukemia, chronic chronic granulocytic leukaemia chronic granulocytic leukemia chronic myelogenous leukaemia chronic myelogenous leukemia chronic myeloid leukaemia	ABCB1 ABCC2 ABCG2 ABL1 ACE AGT AKT1 BCR CASP6 CD36 CD40 CDKN1B CRKL CYP1A1 CYP3A5 DNMT1 E2F1 EZH2 FAS FASLG FCGR2A FGFR3 GPX1 HES1 HLA-DQA1 HLA-DQB1 IL10 IL1RN MDM2 NCSTN PECAM1 SIPA1 SMAD4 STAT5A TERT TGFB1 USP15 VEGFA XRCC1	1027 1244 1399 1543 1577 1636 1786 183 1869 207 2146 2212 2261 23385 25 2876 3117 3119 3280 355 3557 356 3586 4089 4193 5175 5243 613 6494 6776 7015 7040 7422 7515 839 9429 948 958 9958	Homo sapiens (human)	Alliance of Genome Resources
DOID:9952	acute lymphoblastic leukemia Aliases: ALL acute lymphoblastic leukaemia acute lymphocytic leukaemia precursor lymphoblastic lymphoma/leukemia	ABCB1 ABCC2 ABCG2 ABO BAX BCR CAST CD46 CD79B CD86 CFB CREBBP CSF3 CSPG4 CYP1A1 CYP3A5 DPYD ENG EZH2 F3 FAS FGA FLT3 GNB1 GPI GPX1 HDAC1 HDAC2 HDAC4 HFE HK1 HLA-DQA1 HLA-DQB1 IFNG IKZF1 IL10 IRF4 KDM2B KDM3B KDM6A KMT2A KRAS MEFV MTR MYC NBN NOS3 NOTCH3 NRAS NUP214 PON1 PTEN SNRPE TERT TYMS XRCC1	10320 1244 1387 1440 1464 1543 1577 1806 2022 2146 2152 2243 2322 2782 28 2821 2876 3065 3066 3077 3098 3117 3119 3458 355 3586 3662 3845 4179 4210 4297 4548 4609 4683 4846 4854 4893 51780 5243 5444 5728 581 613 629 6635 7015 7298 7403 7515 8021 831 84678 942 9429 974 9759	Homo sapiens (human)	Alliance of Genome Resources

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