GlyCosmos Portal

Rattus norvegicus (Norway rat)

Summary

Taxonomy ID: 10116
PubChem Taxonomy: 10116

Genes (449) Glycans (773) Glycoproteins (2935) Lectins (166) Pathways (1070)

Displaying entries **76 - 100** of **449** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
313729	ERBB receptor feedback inhibitor 1	Errfi1	endometrial cancer osteoarthritis
25658	glucokinase regulator	Gckr	end stage renal disease type 2 diabetes mellitus
117098	pyruvate dehydrogenase E1 subunit alpha 2	Pdha2	disease of metabolism pyruvate decarboxylase deficiency retinal degeneration spermatogenic failure
25630	pyruvate kinase M1/2	Pkm	disease of metabolism hypertension
24533	lactate dehydrogenase A	Ldha	disease of metabolism hyperglycemia hypertension
60416	phosphofructokinase, platelet	Pfkp	disease of metabolism glycogen storage disease
25741	phosphofructokinase, liver type	Pfkl	disease of metabolism glycogen storage disease
65152	phosphofructokinase, muscle	Pfkm	disease of metabolism glycogen storage disease VII glycogen storage disease
24375	alpha-L-fucosidase 1	Fuca1	diabetes mellitus diabetic retinopathy fucosidosis type 1 diabetes mellitus type 2 diabetes mellitus
25694	hyaluronan synthase 2	Has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
315807	phosphatidylinositol glycan anchor biosynthesis, class B	Pigb	developmental and epileptic encephalopathy 80 sleeping sickness
300284	ALG13, UDP-N-acetylglucosaminyltransferase subunit like 1	Alg13l1	developmental and epileptic encephalopathy 36
299691	cryptochrome circadian regulator 1	Cry1	delayed sleep phase syndrome
29484	solute carrier family 3 member 1	Slc3a1	cystinuria
24385	glucokinase	Gck	coronary artery disease diabetes mellitus familial hyperinsulinemic hypoglycemia 3 gestational diabetes glucose metabolism disease hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young obesity permanent neonatal diabetes mellitus steatotic liver disease type 2 diabetes mellitus
362031	ALG14, UDP-N-acetylglucosaminyltransferase subunit	Alg14	congenital myasthenic syndrome 15
316091	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
361368	LARGE xylosyl- and glucuronyltransferase 1	Large1	congenital muscular dystrophy-dystroglycanopathy type A6 facioscapulohumeral muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B6
306549	protein-O-mannose kinase	Pomk	congenital muscular dystrophy-dystroglycanopathy type A12 hydrocephalus muscular dystrophy-dystroglycanopathy type C12
291212	beta-1,3-N-acetylgalactosaminyltransferase 2	B3galnt2	congenital muscular dystrophy-dystroglycanopathy type A11
362093	WD repeat domain 5	Wdr5	congenital heart disease
25478	mannosidase, alpha, class 2A, member 1	Man2a1	congenital dyserythropoietic anemia systemic lupus erythematosus
24390	beta-1,4-galactosyltransferase 1	B4galt1	congenital disorder of glycosylation type IId congenital disorder of glycosylation
78947	mannosyl-oligosaccharide glucosidase	Mogs	congenital disorder of glycosylation type IIb
94273	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Mgat2	congenital disorder of glycosylation type IIa

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