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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 **7801 - 7825** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:251	alcohol-induced mental disorder	Ankk1 Drd2 Gsr	13489 14782 244859	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080697	Opitz GBBB syndrome Aliases: Opitz G/BBB Syndrome Opitz GBBB syndrome type I	MID1	4281	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060844	Norrie disease Aliases: Episkopi blindness Norrie-Warburg disease atrophia bulborum hereditaria	FZD4	8322	Homo sapiens (human)	Alliance of Genome Resources
DOID:4325	Ebola hemorrhagic fever Aliases: Ebola virus disease	CD163 IL3	3562 9332	Homo sapiens (human)	Alliance of Genome Resources
DOID:14261	fragile X syndrome Aliases: FRAGILE X MENTAL RETARDATION SYNDROME MARKER X SYNDROME MARTIN-BELL SYNDROME	Mmp9	81687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:9455	lipid storage disease Aliases: Lipoid storage diseas inborn lipid storage disorder lipoidosis	Psap Psapl1 Slc7a3 Srebf1 Srebf2	11989 19156 20787 20788 76943	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2799	bronchiolitis obliterans Aliases: Bronchiolitis exudativa Bronchiolitis fibrosa obliterans Obliterative bronchiolitis	Ace Ccl2 Ccl7 Cd86 Csf2 Cxcl9 Foxp3 Gzmb Gzmd Gzme Gzmf Gzmg Il13 Il1rn Il4 Mbl2 Mmp9 Muc1 Nos3 Sftpd Tlr9	11421 12524 12981 14939 14941 14942 14943 14944 16163 16181 16189 17195 17329 17395 17829 18127 20296 20306 20371 20390 81897	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070253	congenital disorder of glycosylation type IIa Aliases: Alkuraya syndrome CDG IIa CDG2A CDGIIa CDGS2 carbohydrate-deficient glycoprotein syndrome, type II congenital disorder of glycosylation, type IIa mental retardation, growth retardation, prominent columella, and open mouth	mgat2	100000478	Danio rerio (zebrafish)	Alliance of Genome Resources
DOID:2957	pulmonary tuberculosis	Akt1 Atf3 C3 Ccl2 Ccr5 Cd14 Cd1d1 Crp Ereg Havcr2 Il13 Il15 Il1rn Il4r Kir3dl1 Lta Plaur Sftpa1 Slc11a1 Tlr4 Tnf	116553 117029 24185 24232 24770 24773 24835 25008 25084 25109 25389 25419 25670 29260 316519 353253 363578 50692 59325 60350 60582	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0111535	progressive osseous heteroplasia Aliases: POH ectopic ossification familial type familial ectopic ossification osteoma cutis	Ctnnb1 Sparc Spp1	24791 25353 84353	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:2349	arteriosclerosis Aliases: Arteriosclerotic vascular disease	ldlr.L ldlr.S tgfb1.L	373644 397757 397778	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:8649	tongue cancer Aliases: malignant neoplasm of tongue	FGFR3 RICTOR	2261 253260	Homo sapiens (human)	Alliance of Genome Resources
DOID:1440	Machado-Joseph disease Aliases: Azorean disease MJD SCA3 spinocerebellar ataxia 3 spinocerebellar ataxia type 3	Atg6	42850	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:9281	phenylketonuria Aliases: Folling's disease PKU maternal phenylketonuria phenylalaninemia	Duox Zw	32974 33477	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060695	hyperekplexia Aliases: Kok disease congenital stiff man syndrome familial startle disease hereditary hyperekplexia startle disease	glc-1 glc-2	172103 180086	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050869	villous adenoma	Rnf43	207742	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:14503	neuronal ceroid lipofuscinosis Aliases: hereditary ceroid lipofuscinosis	PEP4	855949	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:8923	skin melanoma Aliases: cutaneous melanoma malignant ear melanoma malignant lip melanoma malignant lower limb melanoma malignant melanoma of ear and/or external auricular canal malignant melanoma of skin of lower limb malignant melanoma of skin of trunk except scrotum malignant melanoma of skin of upper limb malignant neck melanoma malignant scalp melanoma malignant trunk melanoma malignant upper limb melanoma	Aff4 Arhgap44 Ccl2 Cd40 Ddr1 Fanca Grm1 Icam1 Mmp1a Mmp2 Mmp9 Oca2 Stat3 Tyr	12305 14087 14816 15894 17390 17395 18431 20296 20848 216831 21939 22173 83995 93736	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13413	hepatic encephalopathy Aliases: Portal-systemic encephalopathy	STE6 ZWF1	853671 855480	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080390	nephrotic syndrome type 1 Aliases: Finnish congenital nephrosis	syg-2	181561	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110399	retinitis pigmentosa 37 Aliases: RP37	NR2E3	10002	Homo sapiens (human)	Alliance of Genome Resources
DOID:12802	mucopolysaccharidosis I Aliases: Hurler syndrome Hurler-Scheie syndrome Lipochondrodystrophy MPS I - Hurler syndrome Mucopolysaccharidosis, MPS-I Mucopolysaccharidosis, type 1 iduronidase deficiency disease	Idua	34544	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:4202	brain stem glioma Aliases: Brainstem Neuroglial tumor	ver-1	175182	Caenorhabditis elegans	Alliance of Genome Resources
DOID:1210	optic neuritis	Aqp4 Ccr5 Sod2	117029 24787 25293	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0081102	familial gestational hyperthyroidism	Tshr	25360	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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