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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **7401 - 7425** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
57127	Rh family B glycoprotein	RHBG	Homo sapiens (human)
3420	isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit beta	IDH3B Aliases: RP46	Homo sapiens (human)	Zollinger-Ellison syndrome bipolar disorder blindness cataract cone-rod dystrophy congenital nystagmus corneal disease diabetes mellitus dissociated nystagmus early infantile epileptic encephalopathy eye disease fundus albipunctatus fundus dystrophy glaucoma hidradenitis suppurativa hidradenitis hyperinsulinism hypogonadism intellectual disability keratoconus learning disability obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus pompholyx retinitis pigmentosa 46 retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus stomach cancer stomach carcinoma type 2 diabetes mellitus
9439	mediator complex subunit 23	MED23	Homo sapiens (human)
2745	glutaredoxin	GLRX	Homo sapiens (human)
2059	EGFR pathway substrate 8, signaling adaptor	EPS8	Homo sapiens (human)
9101	ubiquitin specific peptidase 8	USP8	Homo sapiens (human)
23092	Rho GTPase activating protein 26	ARHGAP26	Homo sapiens (human)
8542	apolipoprotein L1	APOL1	Homo sapiens (human)
3575	interleukin 7 receptor	IL7R	Homo sapiens (human)
100431172	killer cell lectin like receptor F2	KLRF2	Homo sapiens (human)
6514	solute carrier family 2 member 2	SLC2A2 Aliases: GLUT-2	Homo sapiens (human)	B-cell lymphoma Fanconi syndrome Laron syndrome X-linked dominant hypophosphatemic rickets abdominal obesity-metabolic syndrome 1 achondroplasia atopic dermatitis breast cancer breast carcinoma cancer carcinoma cardiovascular system disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cystinosis cystinuria dental caries dentin caries dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma essential hypertension familial adenomatous polyposis galactokinase deficiency galactosemia gastrinoma gestational diabetes glomerulonephritis glucose intolerance glucose metabolism disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease heart disease hepatitis C hepatocellular carcinoma hyperglycemia hypertension hypoglycemia hypokalemia hypophosphatemia insulinoma intestinal atresia islet cell tumor kidney disease kidney failure lactic acidosis large intestine cancer liver cancer lung squamous cell carcinoma maturity-onset diabetes of the young melanoma myelomeningocele neonatal diabetes nephritis nephrosis obesity obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteomalacia oxyphilic adenoma papillary renal cell carcinoma permanent neonatal diabetes mellitus placental insufficiency prediabetes syndrome pyoureter renal carcinoma renal cell carcinoma renal glycosuria renal oncocytoma rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma spondyloepimetaphyseal dysplasia, Sponastrime type squamous cell carcinoma steatotic liver disease tethered spinal cord syndrome tongue squamous cell carcinoma transient neonatal diabetes mellitus tropical sprue type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus viral infectious disease
123283	threonyl-tRNA synthetase 3	TARS3	Homo sapiens (human)
7416	voltage dependent anion channel 1	VDAC1	Homo sapiens (human)
120776	olfactory receptor family 2 subfamily D member 2	OR2D2	Homo sapiens (human)
23268	dynamin binding protein	DNMBP	Homo sapiens (human)
23193	glucosidase II alpha subunit	GANAB Aliases: G2AN GIIA GluII KIAA0088 neutral alpha-glucosidase AB	Homo sapiens (human)	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
3059	hematopoietic cell-specific Lyn substrate 1	HCLS1	Homo sapiens (human)
9033	polycystin 2 like 1, transient receptor potential cation channel	PKD2L1	Homo sapiens (human)
85444	leucine rich repeat and coiled-coil centrosomal protein 1	LRRCC1	Homo sapiens (human)
6208	ribosomal protein S14	RPS14	Homo sapiens (human)
55556	enolase superfamily member 1	ENOSF1 Aliases: FUCD HSRTSBETA L-fuconate dehydratase TYMSAS rTS	Homo sapiens (human)	Down syndrome Hailey-Hailey disease Holt-Oram syndrome Klippel-Trenaunay syndrome Marfan syndrome Plasmodium falciparum malaria Rothmund-Thomson syndrome Rubinstein-Taybi syndrome VACTERL association Werner syndrome adult lymphoma arachnoiditis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB cancer central nervous system cancer central nervous system lymphoma cerebral malaria childhood leukemia childhood lymphoma colorectal cancer colorectal carcinoma congenital central hypoventilation syndrome cutaneous mastocytosis cutis laxa diffuse cutaneous mastocytosis embryoma endometrial cancer endometrial carcinoma exanthem gliosarcoma hepatitis B herpes zoster high grade glioma intellectual disability large intestine cancer learning disability leukemia lymphoma mal de Meleda malaria mastocytosis meningitis microphthalmia with limb anomalies mixed glioma mixed sleep apnea nail-patella syndrome obsolete ymphosarcoma obstructive sleep apnea ovarian cancer ovarian carcinoma poikiloderma with neutropenia progeria rabies restrictive dermopathy situs inversus sleep apnea split hand-foot malformation 1 with sensorineural hearing loss stomach cancer stomach carcinoma thrombocytopenia-absent radius syndrome tuberous sclerosis urticaria pigmentosa uterine corpus cancer
23246	BOP1 ribosomal biogenesis factor	BOP1	Homo sapiens (human)
1398	CRK proto-oncogene, adaptor protein	CRK	Homo sapiens (human)
83450	dynein regulatory complex subunit 3	DRC3	Homo sapiens (human)
9818	nucleoporin 58	NUP58	Homo sapiens (human)

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