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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 **7901 - 7925** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source
DOID:0060844	Norrie disease Aliases: Episkopi blindness Norrie-Warburg disease atrophia bulborum hereditaria	fz4	31659	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome Aliases: Berdon syndrome Megacystis microcolon intestinal hypoperistalsis syndrome megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH visceral myopathy	CHRM3 LMOD1 MYH11 MYL9 MYLK	10398 1131 25802 4629 4638	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080055	achondrogenesis type IB Aliases: achondrogenesis Fraccaro type	Slc26a2	117267	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8398	osteoarthritis Aliases: Osteoarthrosis and allied disorder degenerative arthritis degenerative joint disease hypertrophic arthritis osteoarthrosis	C27A7.3 W01F3.2 adm-2 daf-1 daf-2 dbl-1 ddr-2 enpp-1 grd-2 mua-3 mup-4 scav-2 scav-3 sma-6 srp-6 srp-7 ver-1 ver-3 ver-4 zmp-3 zmp-4	174044 175182 175410 176060 176430 176673 176787 176829 178748 179068 179125 179195 179663 179665 179991 180349 180351 180622 181289 181489 186632	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110014	age related macular degeneration 1 Aliases: ARMD1 age related maculopathy 1	gldi-2 him-4	174116 181187	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0081312	T-cell non-Hodgkin lymphoma	fgfr1.L fgfr1.S	397782 399444	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0060371	Parkinson's disease 8 Aliases: autosomal dominant Parkinson disease 8 autosomal dominant Parkinson's disease 8	LRRK1 LRRK2	120892 79705	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060201	amyotrophic lateral sclerosis type 10 Aliases: ALS10 TARDBP-related frontotemporal lobar degeneration with TDP43 inclusions amyotrophic lateral sclerosis 10 amyotrophic lateral sclerosis 10, with or without frontotemporal dementia	TARDBP	23435	Homo sapiens (human)	Alliance of Genome Resources
DOID:9410	panhypopituitarism Aliases: Simmond's disease Simmonds' disease combined pituitary hormone deficiency	Robo1	19876	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080957	primary hypoalphalipoproteinemia 1 Aliases: familial HDL deficiency familial hypoalphalipoproteinemia	ABCA1	19	Homo sapiens (human)	Alliance of Genome Resources
DOID:5614	eye disease	myrf-1 myrf-2	174614 181229	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0110274	autosomal recessive limb-girdle muscular dystrophy	HMGCR JAG2 LAMA2 POGLUT1 POMT2 POPDC3	29954 3156 3714 3908 56983 64208	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081138	agammaglobulinemia 6	Cd79b	15985	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2512	nevoid basal cell carcinoma syndrome Aliases: Gorlin syndrome NBCCS basal cell nevus syndrome	GLI1 PTCH1 SHH SMO	2735 5727 6469 6608	Homo sapiens (human)	Alliance of Genome Resources
DOID:13223	uterine fibroid Aliases: Plexiform leiomyoma UTERUS FIBROMA leiomyoma of Corpus Uteri uterine leiomyoma	Col4a1 vkg	33726 33727	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:6196	reactive arthritis Aliases: Fiessinger Leroy Reiter syndrome Post-bacterial arthropathy Reiter disease Reiter's disease postdysenteric arthropathy	Cyp1a1 H2-D1 H2-K1 H2-M2 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7 H2-T3 Sod2	110557 13076 14964 14972 14990 15006 15007 15013 15015 15018 15043 20656	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:8455	pyridoxine deficiency anemia Aliases: vitamin B6 deficiency syndrome	AHCY	191	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111536	Buschke-Ollendorff syndrome Aliases: BOS dermatofibrosis lenticularis disseminata with osteopoikilosis dermatoosteopoikilosis disseminated dermatofibrosis with osteopoikilosis osteopathia condensans disseminata	Lemd3	380664	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:2799	bronchiolitis obliterans Aliases: Bronchiolitis exudativa Bronchiolitis fibrosa obliterans Obliterative bronchiolitis	Ace Ccl2 Ccl7 Csf2 Il13 Il1rn Il4 Mmp9 Nos3 Sftpd	116553 116630 24310 24600 24770 25350 287287 287561 60582 81687	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0070056	autosomal dominant intellectual developmental disorder 26 Aliases: MRD26 autosomal dominant mental retardation 26 autosomal dominant non-syndromic intellectual disability 26	AUTS2	26053	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070262	congenital disorder of glycosylation type IIj Aliases: CDG IIj CDG syndrome type IIj CDG2J CDGIIdj COG4-CDG Carbohydrate deficient glycoprotein syndrome type IIj Congenital disorder of glycosylation type 2j	COG4 ERS1	850438 856220	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0090055	dystonia 25	Gnal	14680	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:9975	cocaine dependence	Ankk1 Bdnf Chrna3 Chrnb3 Comt Drd2 Egr1 Fos Gabbr1 Gria1 Htr2a Htr2c Htr3a Lrrc7 Manea Ngf Oprd1 Oprk1 Oprm1 Per2 Sirt2 Tenm3	108043 110834 12064 12846 13489 13653 14281 14799 15558 15560 15561 18049 18386 18387 18390 18627 23965 242274 242362 244859 54393 64383	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050419	complement factor I deficiency Aliases: C3 INACTIVATOR DEFICIENCY COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY	Cfi	12630	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050866	oral squamous cell carcinoma Aliases: mouth squamous cell carcinoma	cdh1 clptm1l fgfr4 gapdh	100000160 114424 317743 436653	Danio rerio (zebrafish)	Alliance of Genome Resources

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