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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 **15201 - 15225** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:1074	kidney failure Aliases: renal failure	AMBP CD80 DRD1 EDN1 GFER GRP HIF1A KL MT1E MT1H MT2A NAMPT NPHS1 PARP1 PHEX PPARGC1A RHCG SERPINF1 SLC22A2 SLCO4C1 SPP1 TBXA2R TLR2 TLR4 TNFRSF1B	10135 10891 142 1812 1906 259 2671 2922 3091 353189 4493 4496 4502 4868 51458 5176 5251 6582 6696 6915 7097 7099 7133 9365 941	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080652	calcium oxalate nephrolithiasis	AMBP CASR F2 FN1 IL1RN OXGR1 SLC26A1	10861 2147 2335 259 27199 3557 846	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110065	amelogenesis imperfecta type 1F Aliases: AI1F amelogenesis imperfecta hypoplastic type IF amelogenesis imperfecta type IF	AMBN	258	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060602	alpha-methylacyl-CoA racemase deficiency Aliases: AMACR deficiency	AMACR	23600	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111068	congenital bile acid synthesis defect 4 Aliases: CBAS4 intrahepatic cholestasis with defective conversion of trihydroxycoprostanic acid to cholic acid trihydroxycoprostanic acid in bile	AMACR	23600	Homo sapiens (human)	Alliance of Genome Resources
DOID:8634	prostate carcinoma in situ Aliases: PIN III carcinoma in situ of prostate grade III PIN	AMACR APEX1 AREG ATM AURKB BTG2 CDKN1B CREB3L4 CSF1R CYP19A1 ESR1 FGF6 FGF8 FLT1 FZD4 HDAC1 LEF1 LRP1 MAP2K4 MAP2K6 PHB1 PRSS8 PTGS2 RELA SMAD4 ST14	1027 1436 148327 1588 2099 2251 2253 2321 23600 3065 328 374 4035 4089 472 51176 5245 5608 5652 5743 5970 6416 6768 7832 8322 9212	Homo sapiens (human)	Alliance of Genome Resources
DOID:14525	Reye syndrome Aliases: Reye's syndrome	ALY2 LDB19	853361 854500	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:1686	glaucoma	ALY2 LDB19	853361 854500	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:10534	stomach cancer Aliases: gastric cancer gastric neoplasm	ALY2 BUD2 CYC8 GCY1 GIS1 IDP2 IDP3 LDB19 YBR053C YPR1	850871 851670 851974 852342 852410 853361 853770 854287 854500 855723	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9256	colorectal cancer	ALY2 BUD2 CYC8 ERS1 GIS1 GPX1 GPX2 HXK1 LDB19 OSH2 PBS2 RHO1	850438 850614 851543 851670 852410 852546 853313 853361 853770 853842 854500 856294	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060285	parietal foramina Aliases: Caitlin marks enlarged parietal foramina hereditary cranium bifidum	ALX4	60529	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081046	frontonasal dysplasia 2	ALX4	60529	Homo sapiens (human)	Alliance of Genome Resources
DOID:4926	bronchiolo-alveolar adenocarcinoma Aliases: Bronchioalveolar lung carcinoma Bronchioloalveolar carcinoma Minimally Invasive Lung Adenocarcinoma	ALX4 DNMT1 EGFR EGR1 KRAS TP53	1786 1956 1958 3845 60529 7157	Homo sapiens (human)	Alliance of Genome Resources
DOID:2340	craniosynostosis Aliases: Premature closure of cranial sutures	ALX4 BBS9 FGFR2 FGFR3 FLNA NELL1 NOG SKI TCF12 TWIST1	2261 2263 2316 27241 4745 60529 6497 6938 7291 9241	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112038	non-syndromic X-linked intellectual disability 1 Aliases: MRX1 MRX18 MRX78 X-linked mental retardation 1 X-linked mental retardation 1/78 X-linked mental retardation 18 X-linked mental retardation 78	ALX4 ARX IQSEC2	170302 23096 60529	Homo sapiens (human)	Alliance of Genome Resources
DOID:14213	hypophosphatasia Aliases: deficiency of alkaline phosphatase	ALPL	249	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110913	adult hypophosphatasia Aliases: mild hypophosphatasia	ALPL	249	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110914	infantile hypophosphatasia Aliases: Hops phosphoethanolaminuria	ALPL	249	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110915	childhood hypophosphatasia	ALPL	249	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080326	familial hypertrophic cardiomyopathy	ALPK3 CORIN FHOD3 MYBPC3 MYH15 MYH1 MYH7 MYL9	10398 10699 22989 4607 4619 4625 57538 80206	Homo sapiens (human)	Alliance of Genome Resources
DOID:10459	common cold Aliases: Acute viral rhinopharyngitis Nasopharyngitis - acute Nasopharyngitis, acute acute coryza acute nasopharyngitis acute rhinitis rhino-sinusitis	ALOX5 CX3CL1 IFNA2 IL10 IL1A IL1RN TSLP	240 3440 3552 3557 3586 6376 85480	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080821	exercise-induced bronchoconstriction Aliases: exercise-induced asthma	ALOX5 CCL5 TACR1	240 6352 6869	Homo sapiens (human)	Alliance of Genome Resources
DOID:10247	pleurisy	ALOX5 ANXA1 BDKRB1 BDKRB2 CCL11 CSF3 ELANE ESR1 ICAM1 IL15 IL17A IL1RN NOS2 PLA2G6 PTAFR PTGS2 SERPINE1 TNF	1440 1991 2099 240 301 3383 3557 3600 3605 4843 5054 5724 5743 623 624 6356 7124 8398	Homo sapiens (human)	Alliance of Genome Resources
DOID:10762	portal hypertension	ALOX5 ANGPT2 AVP AVPR1A BDKRB2 CCL2 CPEB1 CPEB4 CX3CL1 DBH EDN1 EDNRA EDNRB F5 FGFR2 HSP90AA1 MTOR NGFR NOS1 NOS3 NR1D1 PRL PTEN PTGS2 REN SERPINF1 TMEM67 TNF VASH1 VEGFA	1621 1906 1909 1910 2153 2263 22846 240 2475 285 3320 4804 4842 4846 5176 551 552 5617 5728 5743 5972 624 6347 6376 64506 7124 7422 80315 91147 9572	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060710	autosomal recessive congenital ichthyosis 2 Aliases: ARCI2 BROCQ congenital ichthyosiform erythroderma nonbullous form NCIE1 nonbullous congenital ichthyosiform erythroderma 1	ALOX12B	242	Homo sapiens (human)	Alliance of Genome Resources

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