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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 **776 - 800** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:3247	rhabdomyosarcoma	ANGPT2 CAD	285 790	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050580	hereditary lymphedema	ANGPT2 CALCRL CELSR1 FLT4 PIEZO1 THSD1 TIE1 VEGFC	10203 2324 285 55901 7075 7424 9620 9780	Homo sapiens (human)	Alliance of Genome Resources
DOID:2920	membranoproliferative glomerulonephritis Aliases: Lobular glomerulonephritis chronic glomerulonephritis, lobular	ANGPT2 CCL2 CCN2 CCR6 CDKN1B CFB CFH CXCR1 EDN1 EP300 F5 FN1 MYOC PFN1 PRF1 SPARC TGFBR2 TSLP	1027 1235 1490 1906 2033 2153 2335 285 3075 3577 4653 5216 5551 629 6347 6678 7048 85480	Homo sapiens (human)	Alliance of Genome Resources
DOID:13025	retinopathy of prematurity Aliases: Retrolental fibroplasia premature retinopathy	ANGPT2 DLL4 EPO EPOR FLT1 HGF HLA-B HLA-DRB1 ICAM1 IGFBP3 IHH IL10 KDR NOS1 NOS2 NOS3 NOTCH1 SERPINE1 SERPINF1 SOD1 VEGFA	2056 2057 2321 285 3082 3106 3123 3383 3486 3549 3586 3791 4842 4843 4846 4851 5054 5176 54567 6647 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050876	Caroli disease	ANGPT2	285	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111061	familial hypobetalipoproteinemia 2 Aliases: FHBL2 combined familial hypolipidemia	ANGPTL3 APOB	27329 338	Homo sapiens (human)	Alliance of Genome Resources
DOID:12971	hereditary spherocytosis Aliases: Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia	ANK1 EPB42 SLC4A1 SPTA1 SPTB	2038 286 6521 6708 6710	Homo sapiens (human)	Alliance of Genome Resources
DOID:2843	long QT syndrome Aliases: LQT long Q-T syndrome	ANK2 ARHGAP36 KCNE1 KCNE2 KCNH2 KCNH6 KCNH7 KCNQ1 KCNQ2 KCNQ3 KCNQ5 SCN5A	158763 287 3753 3757 3784 3785 3786 56479 6331 81033 90134 9992	Homo sapiens (human)	Alliance of Genome Resources
DOID:12849	autistic disorder Aliases: Kanner's syndrome autism autistic disorder of childhood onset childhood autism infantile autism	ANK2 C4B CCL2 CNTNAP2 DAB1 EIF4E EN2 FOXP2 GABRA2 GABRA4 GABRA5 GABRB1 GABRB2 GABRR2 GLO1 GRM8 GRN HLA-DRB1 HRAS HSPD1 IL6 KCNQ3 KDM4C KMT2E LAMB1 MECP2 MET MTR NF1 NLGN1 NLGN3 NLGN4X NTRK2 PECAM1 PIK3CG PTCHD1 RELN RPP25 SETDB1 SHANK2 SLC25A12 SLC6A4 SLC9A9 TNF VLDLR	139411 1600 1977 2020 22871 22941 23081 2555 2557 2558 2560 2561 2570 26047 2739 285195 287 2896 2918 3123 3265 3329 3569 3786 3912 4204 4233 4548 4763 4915 5175 5294 54413 54913 55904 5649 57502 6347 6532 7124 721 7436 8604 93986 9869	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111700	ankyrin-B-related cardiac arrhythmia Aliases: ankyrin-B syndrome	ANK2	287	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050824	sinoatrial node disease Aliases: SA node sinuatrial node	ANK2	287	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081202	autosomal recessive intellectual developmental disorder 37	ANK3	288	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050946	Charlevoix-Saguenay spastic ataxia	ANKFY1 SACS	26278 51479	Homo sapiens (human)	Alliance of Genome Resources
DOID:14780	KBG syndrome	ANKRD11	29123	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111133	focal segmental glomerulosclerosis 8 Aliases: FSGS8	ANLN	54443	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090052	dystonia 24	ANO3	63982	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L Aliases: LGMD2L muscular dystrophy, limb-girdle, type 2L	ANO5 FKTN	203859 2218	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070201	Miyoshi muscular dystrophy 3 Aliases: MMD3 Miyoshi myopathy 3	ANO5	203859	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111338	isolated elevated serum creatine phosphokinase levels Aliases: elevated serum CPK idiopathic hyperCKemia isolated hyperCKemia	ANO5	203859	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111533	gnathodiaphyseal dysplasia Aliases: GDD Levin syndrome 2 gnathodiaphyseal sclerosis osteogenesis imperfecta with unusual skeletal lesions osteogenesis imperfecta, Levin type	ANO5	203859	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111052	Scott syndrome Aliases: BDPLT7 SCTS bleeding abnormality due to deficiency of platelet biding of factor X familial prothrombin consumption inhibitor familial prothrombin conversion defect platelet-type bleeding disorder 7 prothrombin consumption deficiency	ANO6	196527	Homo sapiens (human)	Alliance of Genome Resources
DOID:3614	Kallmann syndrome Aliases: Hypogonadism with anosmia Kallman syndrome Kallman's syndrome familial hypogonadism with anosmia	ANOS1	3730	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090094	hypogonadotropic hypogonadism 1 with or without anosmia Aliases: dysplasia olfactogenitalis of de morsier	ANOS1	3730	Homo sapiens (human)	Alliance of Genome Resources
DOID:1508	candidiasis Aliases: Disseminated candidiasis systemic candidiasis	ANP32B ANP32E ARPC5 ARPC5L CCT2 DHX36 EIF4E ELOA2 ELOA FTH1 FUT3 FUT4 FUT5 FUT6 FUT7 FUT9 LTF PRKD2 RRAGC SEC13 SMAP1 SMAP2 SMARCE1 UBXN4	10092 10541 10576 10690 170506 1977 23190 2495 2525 2526 2527 2528 2529 25865 4057 51224 60682 6396 64121 64744 6605 6924 81611 81873	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060081	triple-receptor negative breast cancer	ANTXR1 BARHL1 KDM6A	56751 7403 84168	Homo sapiens (human)	Alliance of Genome Resources

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