GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **101 - 125** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0110860	polycystic kidney disease 3 Aliases: Apkd3 Pkd3 Polycystic Kidney Disease, Adult, Type III	aagr-4	180400	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1574	alcohol use disorder Aliases: Ethanol abuse alcohol abuse	W01F3.2 acr-2 acr-3 cpl-1 dop-1 dop-4 egl-3 gab-1 gbb-2 glp-1 glr-1 glr-2 let-23 lev-1 lin-12 ncam-1 npr-11 pkc-2 sph-1 tbh-1 unc-29 unc-38 unc-47 unc-63 zmp-2 zmp-4	172105 172150 172703 174462 175383 175999 176204 176282 176286 176431 176691 177608 178269 179412 179991 180111 180351 180418 180714 180936 180937 181166 181639 182921 183715 191240	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110460	dilated cardiomyopathy 2A Aliases: CMD2A	Tnni3	21954	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13544	low tension glaucoma Aliases: Normal tension glaucoma	glt-4	188744	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111263	combined malonic and methylmalonic acidemia Aliases: CMAMMA combined malonic and methylmalonic aciduria	ACSF3	197322	Homo sapiens (human)	Alliance of Genome Resources
DOID:14789	spondyloepiphyseal dysplasia congenita Aliases: Late Spondyloepiphyseal Dysplasia	col2a1	394828	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:9513	plasma cell leukemia Aliases: plasma cell leukaemia plasmacytic leukaemia plasmacytic leukemia	CD40 TERT	7015 958	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110461	X-linked dilated cardiomyopathy Aliases: CMD3B DMD-related dilated cardiomyopathy	Dmd	13405	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2033	communication disorder	Col6a3 Ddb1	12835 13194	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110196	Charcot-Marie-Tooth disease type 4G Aliases: CMT4G Charcot-Marie-Tooth neuropathy type 4G HMSNR autosomal recessive Charcot-Marie-Tooth disease type 4G hereditary motor and sensory neuropathy Russe type	Hex-t2	43191	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:3883	Lynch syndrome Aliases: COCA 1 HNPCC - hereditary nonpolyposis colon cancer Hereditary Defective Mismatch Repair syndrome Hereditary non-polyposis colon cancer Hereditary non-polyposis colon cancer syndrome Hereditary non-polyposis colorectal cancer Hereditary non-polyposis colorectal cancer syndrome Hereditary nonpolyposis colon cancer Hereditary nonpolyposis colon cancer syndrome Hereditary nonpolyposis colorectal cancer syndrome hereditary nonpolyposis colorectal cancer hereditary nonpolyposis colorectal neoplasm	acvr2a.L	399283	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0080459	developmental and epileptic encephalopathy 12 Aliases: DEE12 early infantile epileptic encephalopathy 12	PLCB1	23236	Homo sapiens (human)	Alliance of Genome Resources
DOID:9563	bronchiectasis Aliases: Polynesian bronchiectasis	W01F3.2 zmp-4	179991 180351	Caenorhabditis elegans	Alliance of Genome Resources
DOID:10591	pre-eclampsia Aliases: gestational hypertension hypertension induced by pregnancy pre-eclamptic toxaemia preeclampsia preeclampsia/eclampsia pregnancy associated hypertension pregnancy toxemia proteinuric hypertension of pregnancy toxaemia of pregnancy	ACE ACVR2B ADD1 AGT AKR1C3 ALB APELA ARID1A ATP2B4 C3 CALB1 CCL5 CCN3 CD274 CD40 CD40LG CD46 CHI3L1 CLU COMT CORIN CREBBP CUBN CYP11B2 CYP24A1 CYP27B1 CYP2J2 CYP2R1 DNAH8 EBI3 EDN2 ENG ENTPD1 EPAS1 ERBB2 F2 F2R F3 F5 FAS FASLG FLT1 GATA2 GC GPX1 GPX3 GSN HIF1A HLA-A HLA-DQB1 HNF1A HP HSD11B1 ICAM1 IL1RN IL6 ITGA4 ITGAM ITPR1 ITPR2 ITPR3 KCNN4 LCN2 LEP LEPR MMP2 MMP9 NOS3 NOTCH2 NR1H3 OGG1 PDCD1 PDE5A PEG10 PGF PLAUR PPARG PROC PTGS1 PTPN2 RBP4 ROBO1 ROBO4 RYR1 RYR2 RYR3 SERPINA1 SERPINE1 SERPINF2 SLC2A1 TFPI TIMP1 TLR3 TLR4 TNF TNFRSF1B TRPV5 TRPV6 VEGFA	100506013 10062 10148 10699 1116 118 1191 120227 1312 1387 1573 1585 1591 1594 1636 1769 183 1907 2022 2034 2064 213 2147 2149 2152 2153 23089 2321 2624 2638 2876 2878 29126 2934 3091 3105 3119 3240 3290 3383 355 3557 356 3569 3676 3684 3708 3709 3710 3783 3934 3952 3953 4179 4313 4318 4846 4853 4856 493 4968 5054 5133 5228 5265 5329 5345 54538 5468 55503 5624 56302 5742 5771 5950 6091 6261 6262 6263 6352 6513 6927 7035 7076 7098 7099 7124 7133 718 7422 793 8029 8289 8644 8654 93 953 958 959	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080546	non-alcoholic fatty liver Aliases: NAFL nonalcoholic fatty liver	ngf.S	108709389	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0070355	overactive bladder syndrome Aliases: OAB overactive bladder urge syndrome urgency-frequency syndrome	Bdkrb1 Cd40lg Crp Ngf Penk Trpa1	25419 29237 310738 312896 81509 84349	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:705	Leber hereditary optic neuropathy Aliases: Leber's hereditary optic neuropathy Leber's optic atrophy	ENV9	854420	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0070521	peeling skin syndrome 2 Aliases: PSS2	TGM5	9333	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111394	mucopolysaccharidosis type IIIB Aliases: MPS3B MPSIIIB Mucopoly-saccharidosis type 3B Mucopolysaccharidosis type 3B N-acetyl-alpha-glucosaminidase deficiency NAGLU deficiency Sanfilippo syndrome type B mucopolysaccharidosis type IIIB (Sanfilippo B)	GNS NAGLU SGSH	2799 4669 6448	Homo sapiens (human)	Glyco-Disease Genes Database Glyco-Disease Genes Database Glyco-Disease Genes Database Alliance of Genome Resources
DOID:0111805	syndromic microphthalmia 6 Aliases: Bakrania-Ragge syndrome MCOPS6 anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia microphthalmia and pituitary anomalies microphthalmia with brain and digit anomalies syndromic microphthalmia type 6	dbl-1	179068	Caenorhabditis elegans	Alliance of Genome Resources
DOID:9351	diabetes mellitus Aliases: diabetes	Abcg2 Apob Aqp1 Aqp4 Bmp6 Cd40lg Cdh1 Cftr Cpb2 Cyp1a1 Dll4 F7 Fuca1 G6pd Gck Ggt1 Gipr Hfe Hgf Hmgcr Hp Icam1 Igf1r Il10 Il2ra Ins1 Ins2 Insrr Kcnj11 Lrp1 Ogt Pdx1 Ppara Ptprn2 Ptprn Serpine1 Shbg Slc22a12 Slc2a1 Slc2a3 Sod3 Tfpi Tgfb1 Timp1 Tlr4 Vim	113936 116510 116568 116660 24255 24296 24375 24377 24385 24446 24464 24505 24506 24617 24775 24778 25024 25240 25293 25325 25352 25464 25551 25644 25675 25704 25718 25747 260320 26295 29199 29260 29436 29535 29714 299858 311332 312382 365398 54225 59086 60663 81818 83502 83535 84349	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110728	neuronal ceroid lipofuscinosis 5 Aliases: CLN5 neuronal ceroid lipofuscinosis 5 variable age of onset	CLN5	1203	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050694	Brown-Vialetto-Van Laere syndrome	rft-2	178842	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0080807	autosomal dominant craniodiaphyseal dysplasia	Sost	74499	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2738	pseudoxanthoma elasticum Aliases: Gronblad-Strandberg syndrome	vegfaa xylt1 xylt2	30682 560951 563446	Danio rerio (zebrafish)	Alliance of Genome Resources

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