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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 **2226 - 2250** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:13628	favism	G6pd2 G6pdx	14380 14381	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:10763	hypertension Aliases: HTN hyperpiesia vascular hypertensive disorder	abo.2 abo.3 abo.4 abo ace chst12 pon2 ugcg	100144634 100497509 448598 548703 548887 549437 549858 550054	Xenopus tropicalis (tropical clawed frog)	Alliance of Genome Resources
DOID:0110771	hereditary spastic paraplegia 18 Aliases: IDMDC SPG18 autosomal recessive spastic paraplegia 18 autosomal recessive spastic paraplegia type 18 intellectual disability, motor dysfunction and joint contractures	erlin2	100151163	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0111257	gamma-glutamyl transpeptidase deficiency Aliases: GGT deficiency GGT1 deficiency GTG deficiency gamma-glutamyl transferase deficiency glutathionuria	Ggt1	116568	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050851	glomerulosclerosis	ACE AGTR1 AGTR2 APOE COL3A1 HBEGF INF2 MMP1 MMP9 PLA2G7 PLEKHA7 PPARG SERPINE1 SHC1 SPP1	1281 144100 1636 1839 185 186 348 4312 4318 5054 5468 64423 6464 6696 7941	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080119	mitochondrial DNA depletion syndrome 1 Aliases: mitochondrial DNA depletion syndrome 1 (MNGIE type) mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related	Tymp	315219	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:4783	mesangial proliferative glomerulonephritis	fbn-1 pat-2	176076 176240	Caenorhabditis elegans	Alliance of Genome Resources
DOID:2908	Treacher Collins syndrome Aliases: Franceschetti syndrome mandibulofacial dysostosis	Eftud2 Tcof1	20624 21453	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050634	alopecia universalis Aliases: ALOPECIA UNIVERSALIS CONGENITA	Il4	287287	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050558	Ullrich congenital muscular dystrophy Aliases: ULLRICH DISEASE Ullrich scleroatonic muscular dystrophy	COL6A1 COL6A3	1291 1293	Homo sapiens (human)	Alliance of Genome Resources
DOID:10123	pigmentation disease	tpcn2	777614	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:5844	myocardial infarction Aliases: Myocardial infarct heart attack	BUD2 CIT1 CIT2 CIT3 CTS2 CYC8 GLR1 LRO1 MDH1 MDH2 MDH3 PEP4 YLR001C ZWF1	850361 850687 851481 851977 852410 853770 853777 853994 855480 855732 855742 855949 856014 856107	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:9744	type 1 diabetes mellitus Aliases: IDDM insulin-dependent diabetes mellitus type I diabetes mellitus	Ace Ache Adrb1 Aldh2 Aoc3 Apob Avp C3 Ccl11 Ccl2 Ccr5 Cd14 Cd28 Cd38 Cd40lg Chi3l1 Crp Eif2ak3 F7 Fas Faslg Fuca1 G6pd Ghr Hp Iapp Icam1 Ifng Igf2 Igfbp3 Il10 Il15 Il1a Il1rn Il2 Il2ra Il4 Ins1 Ins2 Lta Ncam1 Pdx1 Plat Pon1 Ptprn2 Ptprn Reg1a Sele Sell Slc11a1 Slc18a2 Sod2 Tf Tgfb1 Timp1 Tlr4 Tnf Tnfsf4 Ugt1a1 Vcam1 Xylt1	116510 116562 116660 117029 24221 24232 24310 24375 24377 24464 24476 24483 24484 24493 24505 24506 24586 246097 24714 24770 24787 24825 24835 24861 24925 25008 25235 25325 25361 25385 25419 25464 25544 25549 25660 25668 25670 25692 25704 25712 260320 287287 29259 29260 29397 29473 29535 29539 29702 29714 316519 54225 59086 60350 60582 64133 83817 84024 84349 89814 89824	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:14735	hereditary angioedema Aliases: HANE Hereditary angioneurotic edema	Hs3st-B Spn28Dc sca	32918 34091 36411	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080537	hypermanganesemia with dystonia 2	Slc39a14	213053	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0110334	osteogenesis imperfecta type 1 Aliases: OI1 osteogenesis imperfecta type I	Col1a1	12842	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111592	plasminogen deficiency type I Aliases: hypoplasminogenemia	Plg	18815	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2355	anemia Aliases: anaemia	epor.L	734211	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:699	mitochondrial myopathy Aliases: mitochondrial cytopathy	cle-1	172678	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0111122	nephronophthisis 14 Aliases: NPHP14	ZNF423	23090	Homo sapiens (human)	Alliance of Genome Resources
DOID:1240	leukemia	Abo Ace Bcr Cd28 Dot1l Gpx1 Kras Pdgfra Ptpn11 Ptpn6 Tfpi Trp53	110279 11421 12487 14775 15170 16653 18595 19247 208266 21788 22059 80908	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:5082	liver cirrhosis Aliases: Cirrhosis cirrhosis of liver	Acer Ance Atg6 Axn Egfr InR Mdr49 Mdr65 Parp1 Pxn Sb SerT Snmp2 Spn28Dc Tl btl dally htl mys smo	33196 3355109 34091 34189 34805 36428 37455 37895 38326 38726 38868 39013 39564 41958 42160 42549 42850 43222 43565 44885	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:3114	serous cystadenocarcinoma Aliases: serous adenocarcinoma serous carcinoma	LHCGR TP53 XPC	3973 7157 7508	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050439	Usher syndrome	Arsg Clrn1 Ush2a	22283 229320 74008	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081441	Nicolaides-Baraitser syndrome Aliases: Intellectual disability-sparse hair-brachydactyly syndrome SPARSE HAIR-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME	SNF2	854465	Saccharomyces cerevisiae S288C	Alliance of Genome Resources

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