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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 **1326 - 1350** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:4195	hyperglycemia	ADRB1 AKR1B1 AVP CBL CCL11 CYP11A1 CYP2C9 DRD1 EPAS1 F2 F7 GCK GIPR GLP1R GPX1 HCRTR2 HK2 HK3 HKDC1 HP HRH3 HSPD1 HSPG2 HTR2A ICAM1 IL1A IL1RN IL6 ITGAM ITGAV LDHA LEPR MMP9 PCSK1 PDX1 PKLR PLA2G4A PON1 PPARGC1A PRNP PTCH1 SDC1 SOD1 TF TSHB	10891 11255 153 1559 1583 1812 2034 2147 2155 231 2645 2696 2740 2876 3062 3099 3101 3240 3329 3339 3356 3383 3552 3557 3569 3651 3684 3685 3939 3953 4318 5122 5313 5321 5444 551 5621 5727 6356 6382 6647 7018 7252 80201 867	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060180	colitis	ADIPOQ ADRB3 ANXA1 APOA4 ARRB1 BMP6 CAT CCKBR CCL2 CCR1 CD40 CHUK CRHR2 CXCR2 HAVCR1 HLA-B HP HPR ICAM1 ICOS IKBKB IL10 IL17A KDR LCT MIF MSH2 MUC2 NOD2 NOS2 NOS3 NTRK1 NTRK2 PPARGC1A PTGS2 RELA SELL SELP SI TACR1 TACR2 TFF1 TLR3 TLR4 VCAM1	10891 1147 1230 1395 155 26762 29851 301 3106 3240 3250 337 3383 3551 3579 3586 3605 3791 3938 408 4282 4436 4583 4843 4846 4914 4915 5743 5970 6347 6402 6403 64127 6476 654 6865 6869 7031 7098 7099 7412 847 887 9370 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050855	renal fibrosis	ACE ADAM17 AGER CLU CYBB CYP2J2 ECE1 EDNRA ENG FCAR GFER GPR21 GPR52 IFNG KRAS LEPR MMP1 MMP9 PPARGC1A SERPINE1 STAT6 TLR2 TLR4	10891 1191 1536 1573 1636 177 1889 1909 2022 2204 2671 2844 3458 3845 3953 4312 4318 5054 6778 6868 7097 7099 9293	Homo sapiens (human)	Alliance of Genome Resources
DOID:12236	primary biliary cholangitis Aliases: biliary liver cirrhosis cholestatic cirrhosis chronic nonsuppurative destructive cholangitis primary biliary cirrhosis	ABCA1 ABCB4 ABCC2 ACE2 ACE AGT AQP4 CCL5 CCN2 CD14 CD68 COL1A1 CPEB1 CPEB4 CTLA4 DAG1 DNASE1 ENTPD2 FAS HHIP HLA-DQA1 IFNG IL10 IL12A IL12RB1 IL4 IL6 KRT18 LBR LEP LEPR MAS1 MMP13 MMP2 MMP3 MMP9 MUC2 NOS2 NOS3 NR3C1 NUP62 PDE5A PPARGC1A RELA REN RPS6KB1 SLCO1A2 SLCO1C1 SOD2 STAT4 TLR9 TNF UTP4 VEGFA	10891 1244 1277 1490 1493 1605 1636 1773 183 19 23636 2908 3117 3458 355 3565 3569 3586 3592 3594 361 3875 3930 3952 3953 4142 4313 4314 4318 4322 4583 4843 4846 5244 53919 54106 59272 5970 5972 6198 6352 64399 64506 6579 6648 6775 7124 7422 80315 84916 8654 929 954 968	Homo sapiens (human)	Alliance of Genome Resources
DOID:7998	hyperthyroidism Aliases: overactive thyroid	ADIPOQ ANXA1 ANXA2 ANXA5 APOA1 APOA2 APOC3 BDH1 CAT CP CS CTSL CTSV GPX1 HLA-DQB1 IGF1R IL10 MCM7 NR1D1 PCSK1 PPARGC1A SERPINA7 SERPINE1 SLC34A1 SLC9A1 SOD1 TSHR UCP3 UGT1A1 VIM	10891 1356 1431 1514 1515 2876 301 302 308 3119 335 336 345 3480 3586 4176 5054 5122 54658 622 6548 6569 6647 6906 7253 7352 7431 847 9370 9572	Homo sapiens (human)	Alliance of Genome Resources
DOID:3891	placental insufficiency	AGTR1 CYP19A1 EMP2 EPO GRIN1 GRIN2A GRIN2B ITGA2 PDX1 PPARGC1A SERPINE1	10891 1588 185 2013 2056 2902 2903 2904 3651 3673 5054	Homo sapiens (human)	Alliance of Genome Resources
DOID:1287	cardiovascular system disease Aliases: disease of subdivision of hemolymphoid system	ADIPOQ AGER AGT APOA4 APOB CCL2 CD40LG CFH DBI ENPP1 FGB FTO GHRL GIPR GPX1 GPX3 GYS1 HP HSPA1A LIPG MPO PLAUR PPARG PPARGC1A PTGS2 TLR9 UBR1	10891 1622 177 183 197131 2244 2696 2876 2878 2997 3075 3240 3303 337 338 4353 5167 51738 5329 54106 5468 5743 6347 79068 9370 9388 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:11716	prediabetes syndrome Aliases: Prediabetes impaired glucose tolerance prediabetic state	AGT CALCA CCR2 GCG HLA-DRA IL6 KCNJ11 PPARGC1A PTPRN2 RELB SIRT3 SLC4A2 SLC4A8 UCP3	10891 183 23410 2641 3122 3569 3767 5799 5971 6522 729230 7352 796 9498	Homo sapiens (human)	Alliance of Genome Resources
DOID:10376	amblyopia Aliases: lazy eye	ERBB2 ERBB3 ERBB4 NRG1 PPARGC1A	10891 2064 2065 2066 3084	Homo sapiens (human)	Alliance of Genome Resources
DOID:263	kidney cancer Aliases: malignant neoplasm of kidney except pelvis malignant tumour of kidney renal cancer	FGF9 HRAS KRAS LATS1 LATS2 LLGL1 LLGL2 NRAS POLE PPARGC1A SCRIB	10891 2254 23513 26524 3265 3845 3993 3996 4893 5426 9113	Homo sapiens (human)	Alliance of Genome Resources
DOID:1907	malignant fibrous histiocytoma Aliases: Fibroxanthosarcoma MFH	PPARGC1A	10891	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060058	lymphoma Aliases: lymphoid cancer	ATM CHD4 MALT1 PAFAH1B2 RELA	10892 1108 472 5049 5970	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060060	non-Hodgkin lymphoma	ANXA7 ATR CD40 CD79B CTLA4 FCGR2A GPX1 ICAM1 IGF2R KMT2A MALT1 MTSS1 PON1 PRF1 S1PR2 TMEM260	10892 1493 2212 2876 310 3383 3482 4297 5444 545 54916 5551 9294 958 974 9788	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111988	immunodeficiency 12 Aliases: IMD12 combined immunodeficiency due to MALT1 deficiency	MALT1	10892	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060308	autosomal recessive intellectual developmental disorder Aliases: autosomal recessive mental retardation autosomal recessive non-syndromic mental retardation	Cntnap1 Cntnap2 Cntnap4 Cntnap5a Cntnap5b Cntnap5c Tpr Zc3h14	108989 170571 241175 53321 620292 636808 66797 75553	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1470	major depressive disorder Aliases: clinical depression major depression recurrent major depression single major depressive episode unipolar depression	ADCY3 APOA1 APOA4 ARRB1 BDNF CHRM2 CHRNB3 CNTNAP2 CRTC1 CTNND2 EIF4B FOXP2 HSPA1A HSPA1L HTR1B HTR2A HTR2C IL10 IL3 IL5 IL6 MC1R MED12 NOS1 NR3C1 NRG1 NTRK2 PAWR PTEN SLC5A7 SLC6A4 SYN1	109 1129 1142 1501 1975 23373 26047 2908 3084 3303 3305 335 3351 3356 3358 337 3562 3567 3569 3586 408 4157 4842 4915 5074 5728 60482 627 6532 6853 93986 9968	Homo sapiens (human)	Alliance of Genome Resources
DOID:399	tuberculosis	Btnl2 Ccl1 Cd209a Cd209b Cd209c Cd209d Cd274 Cxcl9 Cyp2c29 Ereg H2-Ab1 H2-D1 H2-Eb1 H2-K1 H2-M2 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7 H2-T3 Ifng Ifngr1 Il22 Il22b Il27 Klrk1 Nfe2l2 Pdcd1 Slc11a1 Sp110 Spp1 Tlr1 Tlr2 Tlr6 Tnf Tnfrsf1b	109032 110557 116849 13095 13874 14961 14964 14969 14972 14990 15006 15007 15013 15015 15018 15043 15978 15979 170776 170779 170786 17329 18024 18173 18566 20290 20750 21897 21899 21926 21938 24088 246779 27007 50929 547431 60533 69165	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0112254	hepatic venoocclusive disease with immunodeficiency Aliases: VODI hepatic veno-occlusive disease-immunodeficiency syndrome	Sp110	109032	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110612	primary ciliary dyskinesia 10 Aliases: CILD10 primary ciliary dyskinesia 10 with or without situs inversus	Dnaaf2	109065	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080695	Burn-McKeown syndrome Aliases: Choanal atresia - deafness - cardiac defects - dysmorphism syndrome	TXNL4A	10907	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050753	cerebellar ataxia	AARS1 AARS2 CACNA1A GEMIN5 L2HGDH PNPLA6 PNPLA7 RPGRIP1L SYNE1 VPS13A VPS13C	10908 16 23230 23322 23345 25929 375775 54832 57505 773 79944	Homo sapiens (human)	Alliance of Genome Resources
DOID:1432	blindness Aliases: vision impairment vision loss visual impairment	AQP4 ATP6V0E1 MYO15A PNPLA6 PNPLA7 RPL26 SLC7A14	10908 361 375775 51168 57709 6154 8992	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111271	Oliver-McFarlane syndrome Aliases: OMCS eyelashes long mental retardation long eyelashes-intellectual disability syndrome trichomegaly-retina pigmentary degeneration-dwarfism syndrome	PNPLA6	10908	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111265	Boucher-Neuhauser syndrome Aliases: ataxia-hypogonadism-choroidal dystrophy syndrome	PNPLA6	10908	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110790	hereditary spastic paraplegia 39 Aliases: NTE-related motor neuron disorder NTEMND SPG39 autosomal recessive spastic paraplegia 39 autosomal recessive spastic paraplegia type 39 spastic paraplegia due to NTE mutation spastic paraplegia due to neuropathy target esterase mutation	PNPLA6	10908	Homo sapiens (human)	Alliance of Genome Resources

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