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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 **8801 - 8825** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0014667	disease of metabolism Aliases: metabolic disease	ins.L ins.S	378695 378696	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:1240	leukemia	GCY1 YPR1	851974 854287	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:2977	primary hyperoxaluria	Grhpr	76238	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111039	hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase Aliases: hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency	AHCY	191	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110807	hereditary spastic paraplegia 55 Aliases: SPG55 autosomal recessive spastic paraplegia 55 autosomal recessive spastic paraplegia type 55	MTRFR	91574	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060838	isolated microphthalmia 7 Aliases: MCOP7	gdf3	30125	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0060161	Kennedy's disease Aliases: Kennedy disease SBMA Spinobulbar Muscular Atrophy X-Linked Bulbo-Spinal Atrophy X-linked Spinal and Bulbar Muscular Atrophy spinal bulbar muscular atrophy	gdnf.L	779087	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0081312	T-cell non-Hodgkin lymphoma	Fgfr1 Tp53	24842 79114	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0110633	rigid spine muscular dystrophy 1 Aliases: Eichsfeld type congenital muscular dystrophy MDRS1 RSMD1 RSS SEPN1-related myopathy classic MmD classic multiminicore disease classic multiminicore myopathy congenital merosin-positive muscular dystrophy with early spine rigidity desmin-related myopathy with Mallory bodies desmin-related myopathy with Mallory body-like inclusions early-onset desmin-related myopathy rigid spine syndrome severe classic form minicore myopathy severe classic form multicore myopathy severe classic form multiminicore disease	Selenon	74777	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111446	progressive myoclonus epilepsy 3 Aliases: CLN14 disease EPM3 PME type 3 Progressive myoclonic epilepsy due to KCTD7 deficiency Progressive myoclonus epilepsy type 3 neuronal ceroid lipofuscinosis 14	WHI2	854208	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:234	colon adenocarcinoma Aliases: Colonic adenocarcinoma adenocarcinoma of colon	csf1ra rnaset2	64274 791890	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:0110813	hereditary spastic paraplegia 62 Aliases: SPG62 autosomal recessive spastic paraplegia 62 autosomal recessive spastic paraplegia type 62	Erlin1	226144	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050840	cervical dystonia Aliases: spasmodic torticollis	H2-Ab1	14961	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111594	distal arthrogryposis type 5D Aliases: DA5D distal arthrogryposis type 5 without ophthalmoparesis distal arthrogryposis type 5 without ophthalmoplegia	Ecel1	13599	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:3602	toxic encephalopathy Aliases: neurotoxicity neurotoxicity syndrome	Abcb1a Abcb1b Abcg2 Drd2 Epha4 Ephx1 Igf1r Il10 Slc18a2	13489 13838 13849 16001 16153 18669 18671 214084 26357	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:4362	cervical cancer Aliases: cervical neoplasm cervix cancer cervix uteri cancer neoplasm of uterine cervix tumor of the Cervix Uteri uterine cervical neoplasm	CDC25 PBS2 PCM1	851019 853313 856652	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:5223	infertility	ATM BRCA2 CDC23 CDKN1B CSF1R ESR1 METTL3	1027 1436 2099 472 56339 675 8697	Homo sapiens (human)	Alliance of Genome Resources
DOID:9471	meningitis	HCN1 HCN2 IGF2 PLAU PLAUR	3481 348980 5328 5329 610	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060696	hyperekplexia 1 Aliases: HKPX1	Glra1	25674	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9255	frontotemporal dementia Aliases: Wilhemsen-Lynch disease frontotemporal lobar degeneration multiple system tauopathy with presenile dementia pallidopontonigral degeneration	YPS3 YPS7	850812 851950	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:13223	uterine fibroid Aliases: Plexiform leiomyoma UTERUS FIBROMA leiomyoma of Corpus Uteri uterine leiomyoma	COL4A1 COL4A2 COL6A3 IRS1 TNRC6B TSC2	1282 1284 1293 23112 3667 7249	Homo sapiens (human)	Alliance of Genome Resources
DOID:3748	esophagus squamous cell carcinoma Aliases: SCC of esophagus SCC of oesophagus oesophagus squamous cell carcinoma	Axn Calr Egfr Jra Kdm4B btl cora gbb htl kug nAChRalpha1 nAChRalpha6 nAChRbeta1 nAChRbeta2 ptc	318918 34304 35851 36057 37205 37455 37778 38545 39564 40191 41166 42160 42918 42920 43565	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0080573	congenital disorder of glycosylation Ix Aliases: congenital disorder of glycosylation 1x	Stt3b	68292	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1596	depressive disorder Aliases: mental depression	Adra2a Bax Bdnf Chrm2 Chrna3 Chrnb3 Chrnb4 Crhbp Crhr1 Crhr2 Cyp1a2 Dbh Drd1 Drd2 Drd5 Esr2 Fos Gabra5 Gdnf Gpm6a Gpm6b Gpx1 Gsk3b Htr1a Htr2a Htr3b Il1rn Il6ra Jun L1cam Ncam1 Nefl Ngf Ngfr Npy1r Npy2r Nr3c1 Ntrk2 Oprk1 Panx1 Plp1 Ren1 Slc5a7 Slc6a2 Slc6a4 Snca Sncg Th Trem1 Xirp2	108015 108043 110834 110886 11551 12028 12064 12919 12921 12922 13077 13166 13488 13489 13492 13983 14281 14573 14758 14775 14815 15550 15558 15567 16181 16194 16476 16728 17967 18039 18049 18053 18166 18167 18212 18387 18823 19701 20538 20617 20618 21823 234267 241431 243764 55991 56637 57014 58217 63993	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8670	eating disorder	HDAC4	9759	Homo sapiens (human)	Alliance of Genome Resources

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