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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 **601 - 625** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:11446	sciatic neuropathy	ABCC8 ABCC9 AGT AKAP12 AMIGO3 APOA1 APOE BDKRB1 BDKRB2 BDNF C3 CACNA1D CACNA1H CACNA1I CAPN1 CASP7 CAT CCL2 CCL5 CDKN1B CERS2 CNR2 CREB1 CYP11A1 CYP17A1 DBN1 FAS FGFR1 FTO FUBP1 GC GDNF GFRA1 GFRA3 GPX3 GRIN1 GRIN2B GSK3B HGF HMGB1 HRH3 HSD3B1 ICAM1 IL10 IL1RN IL6 IL6R JAK1 JAM3 KARS1 KCNC4 KCNJ11 LAMP2 LRP1 MAG MAP2 MC4R MMP9 MPZ MTOR NEFH NEFL NEFM NF1 NGFR NLGN2 NLGN3 NRG1 OPRL1 OPRM1 PCNA PCSK5 PDGFRA PDGFRB PLAT PLAU PMP22 PPARGC1A PTAFR QARS1 RANBP1 RANGAP1 REG3G RGMA SCN10A SERPINE1 SERPINF1 SLC17A8 SNW1 SOD1 TIMP3 TLR4 TNF TNFRSF1A TNFRSF1B	10060 1027 10891 11255 1269 130120 1385 1583 1586 1627 183 2260 22938 246213 2475 2638 2668 2674 2676 2878 2902 2904 2932 29956 3082 3084 3146 3283 335 3383 348 355 3557 3569 3570 3586 3716 3735 3749 3767 386724 3920 4035 4099 4133 4160 4318 4359 4741 4744 4747 4763 4804 4987 4988 5054 5111 5125 5156 5159 5176 5327 5328 5376 54413 56963 5724 57555 5859 5902 5905 623 624 627 6336 6347 6352 6647 6833 7078 7099 7124 7132 7133 718 776 79068 823 83700 840 847 8880 8911 8912 9590	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080855	Parkinsonism	ABAT ABCC8 ABCC9 BAD BDNF CASP9 CNR1 COMT COX1 CSF2 CX3CL1 DRD2 DRD3 EGFR ENO2 ESR1 GBA1 GDNF GFRA1 GFRA2 GRM8 GSK3A HSPA1A HSPA9 KCNJ11 LRRK2 MAPT MMP3 NDUFS3 NFKB2 NGF NGFR NOS1 NTRK1 PARK7 PINK1 PTGS2 RELA RET SHH SLC11A2 SLC17A8 SLC6A3 SLC6A4 SRC TNFRSF1B VDAC1	10060 11315 120892 1268 1312 1437 18 1813 1814 1956 2026 2099 246213 2629 2668 2674 2675 2918 2931 3303 3313 3767 4137 4314 4512 4722 4791 4803 4804 4842 4891 4914 572 5743 5970 5979 627 6376 6469 65018 6531 6532 6714 6833 7133 7416 842	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:5844	myocardial infarction Aliases: Myocardial infarct heart attack	ACE2 ACE ADAMTS1 ADD1 ADIPOQ ADRB1 ADRB2 AGER AGT AGTR1 AHSG AIMP1 AKT1 ALDH2 ANGPT1 ANGPT2 ANXA5 APEX1 APOA1 APOA4 APOC3 APOE APOH AVPR1A BDKRB1 BDKRB2 BRINP3 C3 C7 C8A C8B CACYBP CAMK2D CASR CAT CCL2 CCL5 CCN2 CCR2 CCR3 CD14 CD36 CD40LG CD59 CDKN1B CFL1 CHI3L1 CIITA CLU COL1A1 COL3A1 COL4A1 COL6A3 CS CSF2 CSF3 CSNK2A1 CSNK2A3 CTLA4 CTSB CYBB CYP11B1 CYP1B1 CYP2J2 CYP2R1 DAB2 DAG1 DCN DVL1 DYRK1A ECE1 EDN1 EDN2 EDNRA EDNRB EPAS1 EPHB1 EPO EPOR ERBB2 ERBB4 ESR1 F12 F13A1 F2 F3 F5 F7 FGB FLT1 FN1 FOS FTO FZD2 G6PD GATA4 GCLC GP1BA GP6 GPX1 GSK3B GSN HADH HFE HGF HIF1A HMGB1 HP HSD11B2 HSPD1 ICAM1 IGF1R IL10 IL17A IL18BP IL4R IL6R INHBA ITGA2 ITGA3 ITGB1 ITGB3 ITIH4 KCNK2 KCNN4 KDM6A KDR KLK1 LAMP2 LCAT LGALS2 LIPG LPA LPL LRP1 LRP8 LRPAP1 LTA MAP3K7 MDH2 MDK MEF2C MIF MLXIPL MMP13 MMP14 MMP1 MMP2 MMP3 MMP9 MTOR MYH7 NCAM1 NFE2L2 NGF NOS2 NOS3 NPPA NPPB NPR1 NR1H3 NRG1 OLR1 OPA1 OPRD1 OPRK1 PAPPA PCSK2 PDE5A PDGFD PEBP1 PECAM1 PGF PLA2G7 PLAT PLAU PLAUR PLCB1 PLCB3 PON1 POSTN PPARA PPARGC1A PROC PSMA6 PTGIS PTGS2 RAD50 RANBP1 RBP4 REG1A REG1B REN RPS6KB1 RYR1 SDC1 SDC4 SELP SERPINE1 SHH SIRT1 SIRT3 SMAD4 SOD1 SOD2 SOD3 SPARC SPP1 TBX3 TEK TFPI TGFB1 TGFB2 TGFBR1 TGFBR2 THBS1 TLR4 TNC TNF TNFRSF11B TNFRSF14 TNFRSF1A TNFRSF1B TNFSF11 TNFSF4 TREM1 TRPV1 TTN UTS2R VCAN VDAC2 VEGFA VEGFB VWF YBX1	10062 10068 10111 1027 10631 1072 10891 1116 118 1191 120227 1232 1277 1281 1282 1293 1431 1437 1440 1457 1462 1490 1493 1508 153 1536 154 1545 1573 1584 1601 1605 1634 1636 177 183 185 1855 1859 1889 1906 1907 1909 1910 197 2034 2047 2056 2057 2064 2066 207 2099 2147 2152 2153 2155 2161 2162 217 2244 2321 23236 2335 23410 23411 2353 2475 2535 2539 2626 27101 2729 2811 283106 2837 284 285 2876 2932 2934 3033 3077 308 3082 3084 3091 3146 3240 328 3291 3329 335 337 3371 3383 339479 345 348 3480 350 3566 3570 3586 3605 3624 3673 3675 3688 3690 3700 3776 3783 3791 3816 3920 3931 3957 4018 4023 4035 4043 4049 4089 4191 4192 4208 4261 4282 4312 4313 4314 4318 4322 4323 4625 4684 4780 4803 4843 4846 4878 4879 4881 4904 4973 4976 4982 4985 4986 5037 5054 5069 51085 51206 5126 5175 5228 5327 5328 5329 5331 54210 5444 5465 552 5624 5687 5740 5743 5902 59272 5950 5967 5968 5972 6198 623 624 6261 6347 6352 6382 6385 6403 6469 6647 6648 6649 6678 6696 6885 6926 7010 7035 7040 7042 7046 7048 7057 7099 7124 7132 7133 718 7273 7292 729230 730 731 732 7403 7417 7422 7423 7442 7450 7804 79068 7941 80310 817 846 847 8600 8654 8764 9255 929 9370 9388 948 9510 959 966	Homo sapiens (human)	Alliance of Genome Resources
DOID:3526	cerebral infarction Aliases: CVA - Cerebral infarction Cerebral infarct	A2M ACE ADORA1 AGER ANXA1 APOA5 APOB APOE BRINP3 CBS EPHX2 F2 F5 F7 FOLH1 GPX3 GRIN1 GSN HIF1A HLA-A HLA-B HLA-DRB1 HMGB1 HNF1A ICAM1 IFNB1 ITGA9 ITGAM KALRN KCNN4 LIPG LPA LTA MAP2 MTR MYRF NR1H3 PARK7 PDX1 PLA2G7 PON1 PON2 PRKCH PROS1 PTGIS RBP4 SERPINE1 SERPING1 SLC6A1 SOS1 TBXAS1 THBD TNF TNFRSF11B TOMM40 TYMS VIM	10062 10452 11315 116519 134 1636 177 2 2053 2147 2153 2155 2346 2878 2902 2934 301 3091 3105 3106 3123 3146 338 3383 339479 3456 348 3651 3680 3684 3783 4018 4049 4133 4548 4982 5054 5444 5445 5583 5627 5740 5950 6529 6654 6916 6927 7056 710 7124 7298 7431 745 7941 875 8997 9388	Homo sapiens (human)	Alliance of Genome Resources
DOID:13001	carotid stenosis Aliases: Carotid artery stenosis Stenosis, carotid artery	F2 IL10 IL4 LPA MMP1 MMP3 MT2A NR1H3 PLA2G7 PROCR PTGIS TLR2 TLR4 VCAM1	10062 10544 2147 3565 3586 4018 4312 4314 4502 5740 7097 7099 7412 7941	Homo sapiens (human)	Alliance of Genome Resources
DOID:7693	abdominal aortic aneurysm Aliases: AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1	ACE ADM AHCY APOE CCL2 CSF2 ELN EZH2 FASLG FOLH1 FTO HLA-DQA1 HLA-DRB1 IFNG IL10 ITGAM ITGAV KNG1 LOX MMP12 MMP13 MMP14 MMP1 MMP2 MMP3 MMP8 MMP9 MTHFD1 MTR MYH11 NOS2 NR1H3 P2RY12 PLA2G7 PON1 POSTN SELL SERPINE1 SLC19A1 SOD2 SORT1 TYMS	10062 10631 133 1437 1636 191 2006 2146 2346 3117 3123 3458 348 356 3586 3684 3685 3827 4015 4312 4313 4314 4317 4318 4321 4322 4323 4522 4548 4629 4843 5054 5444 6272 6347 6402 64805 6573 6648 7298 79068 7941	Homo sapiens (human)	Alliance of Genome Resources
DOID:1936	atherosclerosis	ADD1 ADIPOQ AGER AGT APOA1 APOE CASR CD36 CD40 CD40LG CLU COL4A2 CPE CSF1 F2 FAS FCGR2A GPX3 GRN HMGB1 HNRNPC HP HPR HSPA1A ITGAM LDLR LPA MMP1 MMP2 NGF NGFR NONO NOS3 NPPB NR1H3 PARP15 PDGFD PECAM1 PLA2G7 PLAU PLTP PON1 PON3 PTGES3 PTGIS RBP4 SELP SIRT1 STAT3 STAU1 UBR1 VIM WIZ	10062 10728 118 1191 1284 1363 1435 165631 177 183 197131 2147 2212 23411 2878 2896 3146 3183 3240 3250 3303 335 348 355 3684 3949 4018 4312 4313 4803 4804 4841 4846 4879 5175 5328 5360 5444 5446 5740 58525 5950 6403 6774 6780 7431 7941 80310 846 9370 948 958 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:5425	ovarian hyperstimulation syndrome Aliases: secondary Meig's syndrome	DRD2 F3 FSHR IL6 KDR NR1H3 SERPINF1 TFPI VEGFA	10062 1813 2152 2492 3569 3791 5176 7035 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:6713	cerebrovascular disease Aliases: CVA cerebrovascular disorder stroke	AGT AGTR1 APOE ARHGEF7 G6PD GLCE GPX3 GRP LMNA NR1H3 P2RY12 SELE	10062 183 185 2539 26035 2878 2922 348 4000 6401 64805 8874	Homo sapiens (human)	Alliance of Genome Resources
DOID:5082	liver cirrhosis Aliases: Cirrhosis cirrhosis of liver	ABCB11 ABCB4 ACE ADAMTS13 ADAR ADIPOQ AGER AGT AKAP12 ALB APOA1 AZGP1 C5 CCL2 CCL5 CCN2 CCR1 CD163 CD36 CENPC CLDN1 CPEB1 CPEB4 CSF1R CYP3A4 CYP3A5 CYP3A7-CYP3A51P CYP3A7 DNMT1 DRD4 EDN1 EGFR EGR1 ELN ENTPD2 F2 F3 F5 FBN1 FGFR4 FLT1 FUBP1 GCLC GDF1 GGT1 GLI3 GLUL GOLM1 GP1BA GPC3 HFE HLA-DPA1 HLA-DQA1 HLA-DQB1 HLA-DRB1 HP HRAS ICAM1 IFNA2 IFNG IGF1R IGF2 IL10 IL18BP IL21 IRF5 ITGB6 ITIH4 KDR KIR3DS1 KLKB1 KRT18 KRT8 LBP LGALS3 MBL2 MMP1 MMP2 MPO MUC2 MYC NFE2L2 NOS3 NPPB PARP1 PDGFB PDGFD PDIA3 PECAM1 PGF PHKG2 PIK3CG PLAUR PNPLA3 PTGS2 RAD50 RBP4 RELA RELN SERPINA1 SERPINE1 SERPINH1 SLC6A4 SMO SOD2 SPAG9 SPINT1 TFPI TGFB1 TGFB2 THPO TLR3 TLR4 TNF UTP4 VASH1 VCAM1 VEGFA VEGFC WDR35 XRCC1	10068 100861540 10111 103 1060 11093 1230 142 1436 1490 1551 1576 1577 1636 177 1786 1815 183 1906 1956 1958 2006 213 2147 2152 2153 2200 2264 22846 2321 2657 2678 2719 2729 2737 2752 2811 2923 3077 3113 3117 3119 3123 3240 3265 335 3383 3440 3458 3480 3481 3586 3663 3694 3700 3791 3813 3818 3856 3875 3929 3958 4153 4312 4313 4353 4583 4609 4780 4846 4879 5054 51280 5155 5175 5228 5244 5261 5265 5294 5329 563 5649 5743 57539 59067 5950 5970 6347 6352 64506 6532 6608 6648 6692 7035 7040 7042 7066 7098 7099 7124 727 7412 7422 7424 7515 80310 80315 80339 84916 8647 871 8880 9043 9076 9332 9370 948 954 9590	Homo sapiens (human)	Alliance of Genome Resources
DOID:1485	cystic fibrosis Aliases: CF mucoviscidosis	ABCB11 ABCB1 ABCB4 ABCB5 ABCC12 ABCC4 ADRB1 ADRB2 ADRB3 AGER C5 CCL11 CCL2 CCR3 CD14 CD40LG CFTR CLCA1 CLCN2 CSF3R CXCR3 CYP1A1 EDEM1 EDN1 FAS FASLG FCGR2A GCLC HAVCR2 HFE HLA-G HSPA1A HSPD1 IGFBP3 IL13 IL17A IL18BP IL1A IL1RN IL6 IL9 IL9R LEP LTA MBL2 MIF MMP9 MPO MUC1 MUC2 MUC5AC MUC5B NOS1 NOS2 NOS3 PPARA PRSS1 PTGDR2 PTGS2 PTX3 SCNN1B SERPINA3 SFTPA1 SFTPB SFTPC SFTPD TGFB1 TIMP1 TLR4 TLR5 TLR9 TNF	10068 10257 1080 11251 1179 1181 12 1232 1441 153 154 1543 155 177 1906 2212 2729 2833 3077 3135 3303 3329 340273 3486 355 3552 3557 356 3569 3578 3581 3596 3605 3952 4049 4153 4282 4318 4353 4582 4583 4586 4842 4843 4846 5243 5244 54106 5465 5644 5743 5806 6338 6347 6356 6439 6440 6441 653509 7040 7076 7099 7100 7124 727 727897 84868 8647 929 94160 959 9695	Homo sapiens (human)	Alliance of Genome Resources
DOID:3083	chronic obstructive pulmonary disease Aliases: COLD COPD chronic obstructive airway disease chronic obstructive lung disease	ABCC1 ACE ADAM33 ADAM9 ADIPOQ ADRB1 ADRB2 AGER BAMBI BDKRB2 C3 C5 C5AR1 CAT CCL11 CCL1 CCL2 CCL5 CCL7 CCN2 CCR3 CCR5 CD28 CD40 CD80 CD86 CFTR CHI3L1 CHRM3 CHRNA3 CHRNA5 CHRNA7 CLCA1 CMA1 COL1A1 CRHR1 CSF2 CTLA4 CXCR2 CXCR3 CYP1A1 CYP1A2 CYP2E1 DEFB1 EDN1 EGFR EGR1 ELN ERBB3 F2 F2RL1 FAIM2 FAS FASLG FLT1 GC GRIK5 GRIN2B GZMA GZMB HDAC2 HHIP HLA-DPB1 HP HSPA4 HTR2A ICAM1 IL12B IL13 IL13RA1 IL16 IL17A IL18BP IL1RL1 IL1RN IL5 IL5RA IL6 IL9 KDR LEP LEPR LRP1B MAP2K4 MBL2 MCAM MMP1 MMP9 MPO MUC1 MUC5AC MUC5B NFE2L2 NOD2 NOS1 NOS2 NR3C1 NTF3 NTRK1 PLAU PLAUR PON1 PPARGC1A PTGS2 SELP SERPINA1 SERPINA3 SERPINE1 SFTPA1 SFTPB SFTPC SFTPD SLC6A4 SMAD4 SMPD3 SOD3 STAT1 STAT4 TGFB1 TIMP1 TLR4 TNF TNFRSF1A TNFRSF1B VEGFA XRCC5	10068 1080 10891 1116 1131 1136 1138 1139 1179 12 1215 1232 1234 1277 1394 1437 1490 1493 153 154 1543 1544 1571 1636 1672 177 1906 1956 1958 2006 2065 2147 2150 23017 2321 25805 2638 2833 2901 2904 2908 3001 3002 3066 3115 3240 3308 3356 3383 355 3557 356 3567 3568 3569 3578 3579 3593 3596 3597 3603 3605 3791 3952 3953 4089 4153 4162 4312 4318 4353 4363 4582 4586 4780 4842 4843 4908 4914 5054 5265 5328 5329 53353 5444 55512 5743 624 6346 6347 6352 6354 6356 6403 64127 6416 6439 64399 6440 6441 6532 653509 6649 6772 6775 7040 7076 7099 7124 7132 7133 718 727 727897 728 7422 7520 80332 847 8754 9173 9370 940 941 942 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:3042	allergic contact dermatitis	CCR1 CCR5 FLT1 IL18BP KDR MMP3 MMP9 TLR4 VEGFA	10068 1230 1234 2321 3791 4314 4318 7099 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:14018	alcoholic liver cirrhosis Aliases: Alcoholic Cirrhosis Alcoholic cirrhosis of liver Laennec's cirrhosis Laennec's cirrhosis, alcoholic Portal cirrhosis	ALDH2 CYP2E1 DDR1 DDR2 GABRG2 IL18BP LEP MMP13 NR1D1 PLAU SERPINE1 SERPINF1 SOD2 TG TLR9	10068 1571 217 2566 3952 4322 4921 5054 5176 5328 54106 6648 7038 780 9572	Homo sapiens (human)	Alliance of Genome Resources
DOID:3565	meningioma Aliases: meningeal neoplasm meningothelial cell tumor neoplasm of the meninges primary Meningeal tumor	Arhgap28 Epb41l3 Hgf Spon2	100689 13823 15234 268970	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9970	obesity	Abca1 Abcg5 Abcg8 Acacb Ace Acsl1 Adamts20 Adamts4 Adipoq Adora1 Adrb2 Adrb3 Ager Ahsg Ak1 Akt2 Aldh1a1 Aldh1b1 Aldh2 Alms1 Amh Angptl6 Aoc3 Apob Apoc3 Apod App Atp4b Atp5f1b Atp5f1c Azgp1 Bad Bdnf Bmp5 Bmp6 Bmp7 Bmp8a Bmp8b Bnip3 C3 C5ar1 Cadm2 Canx Cckar Ccl2 Ccl7 Cd36 Cd40 Cd40lg Cfd Cnr1 Col1a1 Col3a1 Col4a1 Comt Cpb2 Cpe Cps1 Cpt1a Crhbp Crhr1 Cst3 Ctnnb1 Ctsc Dchs1 Dcn Drd1 Drd2 Drd4 Eif6 Enpp1 Esr1 Esr2 F2 F7 Fads1 Fat4 Fgfr1 Fgg Fjx1 Flii Foxc2 Fto G6pd2 G6pdx Gabra6 Gapdh Gck Gfpt1 Ghsr Gipr Glp1r Glul Gnas Gnrhr Gorasp2 Gpr12 Gpx1 Gucy2c Hdac4 Hdac6 Hfe Hgf Hk1 Hk2 Hmgcs1 Hp Hrh3 Hsd11b1 Hsd17b4 Hspa1a Htr1b Htr2a Htr2c Icam1 Ifng Igf1r Igfbp3 Il10 Il15 Il1rn Il3 Il6ra Inppl1 Irs1 Itgam Itih4 Itpr1 Itpr3 Jup Kdm3a Lbp Lcn2 Lep Lepr Lipc Lipg Lpl Mapt Mbl2 Mc3r Mc4r Mchr1 Mmp9 Mtor Myc Nampt Ncoa1 Neil1 Nfe2l2 Nmur1 Nmur2 Nos3 Notch1 Notch2 Notch3 Nox4 Npy1r Npy2r Npy5r Nr3c1 Nucb2 Oprm1 Pcsk1 Pcsk1n Pdx1 Pgf Pik3r1 Plat Plaur Plcb3 Plin1 Plin2 Plin3 Plxnb1 Plxnb2 Plxnb3 Plxnd1 Pnpla2 Pnpla3 Pomc Pon2 Ppara Pparg Ppargc1a Prkaa1 Prkaa2 Prkcb Prkci Prlhr Ptprf Pum1 Pum2 Rbp4 Rela Ren1 Rps6kb1 Sdc1 Sdc3 Sdk1 Sdk2 Sec16a Selp Serpina12 Serpinf1 Sftpb Sirt6 Slc10a1 Slc15a1 Slc15a2 Slc2a1 Slc6a14 Slc6a3 Snap25 Sorbs1 Srebf2 Stat3 Stim1 Stim2 Tbc1d5 Tcf12 Tcf4 Tcf7l2 Tgfb1 Th Thbd Thbs1 Timp1 Tlr4 Tnf Tnfrsf1a Trf Tsc1 Tulp1 Ucp2 Vwf Wdtc1 Wnt10b Wnt1 Zfhx2 a	100705 103968 103988 104263 105787 108079 11303 11421 11450 11520 11537 11539 11555 11556 11596 11625 11636 11652 11668 11669 116873 116939 11705 11754 11814 11815 11820 11945 11947 11949 12007 12015 12064 12160 12161 12162 12163 12164 12176 12266 12273 12330 12387 12425 12491 12801 12825 12826 12842 12846 12876 12894 12919 12921 13010 13032 13162 13179 13488 13489 13491 13982 13983 140570 140571 14061 14068 14081 14182 14221 14234 14248 14380 14381 14399 14433 14583 14645 14652 14683 14715 14738 14767 14775 14815 14917 15185 15216 15234 15275 15277 15439 15450 15483 15488 15551 15558 15560 15894 15978 16001 16009 16153 16168 16181 16187 16194 16332 16367 16409 16418 16427 16438 16440 16480 16803 16819 16846 16847 16891 16956 17195 17201 17202 17395 17762 17869 17977 18024 18127 18128 18129 18131 18166 18167 18168 18390 18548 18605 18609 18654 18708 18751 18759 18791 18793 18797 18976 19013 19016 19017 19268 193740 19662 19697 19701 20296 20306 20317 20344 20388 20411 20493 20525 20614 20788 207911 208188 20848 20866 208715 208727 20969 20970 21406 21413 21416 216749 21803 21823 21824 21825 21857 21898 21926 21937 21939 21947 22041 22157 22228 22371 223838 22408 22410 226278 227231 227648 230796 233651 235611 236266 237979 238055 239102 239857 240913 26383 27409 30052 329628 330222 330260 381853 50490 50518 50721 53322 56373 56643 56717 56774 57738 59027 64930 66853 66905 67470 67784 68054 70231 70726 72238 72508 72535 72774 76267 80912 80913 99296 99571	Mus musculus (house mouse)	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	Abcb1b Abcc2 Abcc3 Abcg5 Abcg8 Acaca Acacb Acadm Acadvl Actb Adamts13 Adipoq Adrb3 Ahcy Ahcyl Akt1 Aldh2 Atp5f1a Azgp1 Ccl2 Cd163 Col1a1 Dgat2 Ezh2 Fasn Foxo1 Fto G6pd2 G6pdx Gpt Gsr Hadha Hfe Hmgcr Hp Ifna11 Ifna12 Ifna13 Ifna16 Ifna1 Ifna4 Ifna9 Igf1r Igfbp7 Il10 Il13 Il1rn Insr Irs1 Irs2 Krt18 Lep Lepr Lpl Mlxipl Mlycd Nampt Nfe2l2 Pla2g7 Plin1 Plin2 Plin3 Pnpla3 Pon2 Ppargc1a Sidt2 Sirt2 Sirt4 Sirt6 Slc7a3 Sod2 Srebf1 Stat3 Tfrc Tg Tlr4 Tlr9 Tnf Ubr2 Ucp2	100705 103968 107476 11364 11370 11450 11461 11520 11556 11615 11651 11669 116939 11946 11989 12007 12780 12842 14056 14104 14380 14381 14782 15216 15357 15439 15962 15964 15967 15972 16001 16153 16163 16181 16337 16367 16668 16846 16847 16956 18024 18669 19017 20296 20656 20787 20848 214597 21819 21898 21926 22042 22228 224826 230396 230398 242519 26383 269378 27226 27409 279028 29817 330260 384783 50721 56458 56690 58805 59027 64383 66905 67470 67800 75387 76282 76408 81897 93671 97212	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9452	steatotic liver disease Aliases: Fatty change of liver SLD Steatosis of liver alcoholic fatty liver fatty liver disease hepatic lipidosis hepatic steatosis	Abca1 Abcc2 Abcc3 Acaca Acacb Adipoq Adrb2 Ahcy Ahcyl Alpl Apob Cd163 Cpe Cps1 Ctsb Dgat2 Fgfr1 G6pc1 Gck Ggt1 Gpt Gpx1 Hadha Hspa5 Htr2a Htr2b Il10 Il13ra2 Ins1 Ins2 Insr Ldlr Lep Lrp6 Mc4r Nfkb1 Nox4 Pnpla3 Ppara Pparg Ppargc1a Ptgs2 Rela Sec63 Slco1a4 Ucp2	100705 103988 107476 11303 11450 11555 11615 11647 116939 12780 12876 13030 140740 14182 14377 14598 14775 14828 15558 15559 16153 16165 16333 16334 16337 16835 16846 16974 17202 18033 19013 19016 19017 19225 19697 22228 227231 238055 269378 28250 50490 67800 76282 76408 93671 97212	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080000	muscular disease	Acaca Acacb Clu Cpt2 Fasn Hmgcr Itga7 Lpl Nmt1	100705 107476 12759 12896 14104 15357 16404 16956 18107	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060404	chromosome 17q12 deletion syndrome Aliases: 17q12 microdeletion syndrome	Acaca Acacb	100705 107476	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0060309	syndromic X-linked intellectual disability Aliases: syndromic X-linked mental retardation	ARX ATP6AP2 CASK DDX3X HUWE1 NKAP PHF2 PHF8 ZFX	10075 10159 1654 170302 23133 5253 7543 79576 8573	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060811	syndromic X-linked intellectual disability Turner type Aliases: Brooks-Wisniewski-Brown syndrome MRXST X-linked intellectual disability, Brooks type mental retardation and macrocephaly syndrome mental retardation, X-linked syndromic, Turner type	HUWE1	10075	Homo sapiens (human)	Alliance of Genome Resources

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