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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **7851 - 7875** of **7942** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism
DOID:987	alopecia	ABO ACAT1 ACE ACER1 AGA AGXT AKR1C4 ALOX12B ATP6V0A2 CERS3 CYP17A1 CYP19A1 CYP27B1 DCN DGAT1 EBP EOGT FADS2 FAR2 FUT3 HPGDS HSD11B1 HSD3B1 ICAM1 KDSR KLRK1 LSS PARP1 PCYT1A PLCD1 PNPLA6 PRNP PRSS8 PTGDS PTGS2 SHMT1 SOAT1 SRD5A1 SRD5A2 ST3GAL4 STS VCAN	10682 10908 1109 125981 142 1462 1586 1588 1594 1634 1636 175 189 204219 22914 23545 242 2525 2531 27306 28 285203 3283 3290 3383 38 4047 412 5130 5333 55711 5621 5652 5730 5743 6470 6484 6646 6715 6716 8694 9415	Homo sapiens (human)
DOID:3534	Lafora disease Aliases: Lafora Progressive Myoclonic Epilepsy Lafora's disease MYOCLONIC EPILEPSY OF LAFORA	gys1 gys2	373082 394155	Danio rerio (zebrafish)
DOID:10022	ampulla of Vater benign neoplasm Aliases: tumor of the ampulla of Vater	CALR	811	Homo sapiens (human)
DOID:0060479	Shwachman-Diamond syndrome Aliases: Shwachman syndrome Shwachman-Bodian-Diamond syndrome Shwachman-Diamond type metaphyseal dysplasia pancreatic insufficiency and bone marrow dysfunction	CYP2E1 LYZ PAFAH1B1 PTEN PTGS2	1571 4069 5048 5728 5743	Homo sapiens (human)
DOID:1588	thrombocytopenia	Tnf	24835	Rattus norvegicus (Norway rat)
DOID:224	transient cerebral ischemia Aliases: TIA TIA - Transient ischaemic attack Transient cerebral ischaemia Transient ischemic attacks transient ischemic attack	G6pd2 G6pdx Got1 Nampt Ogg1 Pcna Sirt6 Tnf Ucp2	14380 14381 14718 18294 18538 21926 22228 50721 59027	Mus musculus (house mouse)
DOID:8577	ulcerative colitis Aliases: Left-sided ulcerative colitis	Igf2 Tnf	24483 24835	Rattus norvegicus (Norway rat)
DOID:12798	mucopolysaccharidosis	Gusb Hyal1	110006 15586	Mus musculus (house mouse)
DOID:7519	endocervical carcinoma Aliases: carcinoma of endocervix carcinoma of the Endocervix	PTGS2	5743	Homo sapiens (human)
DOID:9352	type 2 diabetes mellitus Aliases: NIDDM insulin resistance non-insulin-dependent diabetes mellitus type 2 diabetes type II diabetes mellitus	W03G11.3 aldo-1 cht-1 gpdh-3 gspd-1 ogt-1 parp-1 ugt-62	172509 175591 176000 176788 178046 180628 189173 266823	Caenorhabditis elegans
DOID:37	skin disease Aliases: Genodermatosis skin and subcutaneous tissue disease	Tnf	21926	Mus musculus (house mouse)
DOID:14764	Larsen syndrome Aliases: dominant larsen syndrome	CHST3	9469	Homo sapiens (human)
DOID:5504	tanycytic ependymoma	AKR1A1 ASAH1 CALR CD38 CD44 CHI3L1 IDH1 IDH2 IL18R1 IL1R1 L1CAM PIK3CA PIK3CB PIK3CD PIK3CG PTEN PTGS2 TDG TNFRSF10C	10327 1116 3417 3418 3554 3897 427 5290 5291 5293 5294 5728 5743 6996 811 8794 8809 952 960	Homo sapiens (human)
DOID:8552	chronic myeloid leukemia Aliases: CML CML - chronic Myelogenous Leukemia Myeloid Leukemia, chronic chronic granulocytic leukaemia chronic granulocytic leukemia chronic myelogenous leukaemia chronic myelogenous leukemia chronic myeloid leukaemia	Akt1	11651	Mus musculus (house mouse)
DOID:8778	Crohn's disease Aliases: Crohn disease Crohn's disease of colon Crohn's disease of large bowel Granulomatous Colitis Pediatric Crohn's disease	ATG26	850886	Saccharomyces cerevisiae S288C
DOID:10652	Alzheimer's disease Aliases: Alzheimer disease Alzheimers dementia	Apod Bad Eno1 Gapdh Gapdhs Gsk3b Gsto2 Htr2a Igf2 Ins1 Ins2 Lep Parp1 Pck1 Pik3r1 Ppara Ppargc1a Tlr4 Tnf	24333 24383 24483 24505 24506 24835 25239 25513 25591 25608 25747 29260 29595 309465 362282 64639 66020 83516 84027	Rattus norvegicus (Norway rat)
DOID:3762	cytochrome-c oxidase deficiency disease Aliases: MITOCHONDRIAL COMPLEX IV DEFICIENCY	CHKB EHHADH GAA GBE1 HADHA OTOA PLCE1 PTGS1 PTGS2 SIRT4	1120 146183 1962 23409 2548 2632 3030 51196 5742 5743	Homo sapiens (human)
DOID:0111460	cardiofaciocutaneous syndrome 1 Aliases: CFC1	BRAF CFC1	55997 673	Homo sapiens (human)
DOID:10140	dry eye syndrome Aliases: Tear film insufficiency dry eye disease	Tlr4	29260	Rattus norvegicus (Norway rat)
DOID:4137	common bile duct disease	Slc25a13	50799	Mus musculus (house mouse)
DOID:0080575	Larsen-like syndrome B3GAT3 type Aliases: Larsen-like syndrome, B3GAT3 type multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome	GlcAT-I	251900	Drosophila melanogaster (fruit fly)
DOID:0060391	chromosome 13q14 deletion syndrome Aliases: deletion 13q14	CYP11A1 FREM1 PAFAH1B1 PRNP	1583 158326 5048 5621	Homo sapiens (human)
DOID:0080573	congenital disorder of glycosylation Ix Aliases: congenital disorder of glycosylation 1x	STT3B	201595	Homo sapiens (human)
DOID:13186	megaesophagus	AGA CALR ECI1 FUT3 GMPPA	1632 175 2525 29926 811	Homo sapiens (human)
DOID:0060074	ductal carcinoma in situ	Tp53 Tymp	24842 315219	Rattus norvegicus (Norway rat)

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