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 **126 - 150** of **449** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
306860	glucosaminyl (N-acetyl) transferase 2	Gcnt2	cataract 13 with adult i phenotype cataract
297508	nicotinamide phosphoribosyltransferase	Nampt	carotid artery disease coronary artery disease kidney failure metabolic dysfunction-associated steatotic liver disease middle cerebral artery infarction obesity periodontitis psoriasis pulmonary hypertension transient cerebral ischemia type 2 diabetes mellitus
114104	N-acylsphingosine amidohydrolase 2	Asah2	cardiomyopathy
83688	transaldolase 1	Taldo1	carbohydrate metabolic disorder
300741	mannose phosphate isomerase	Mpi	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
296564	fucosyltransferase 7	Fut7	candidiasis
84597	fucosyltransferase 9	Fut9	candidiasis
60670	fucosyltransferase 4	Fut4	candidiasis
303872	phosphatidylinositol glycan anchor biosynthesis, class Z	Pigz	cancer
24668	protein phosphatase 1 catalytic subunit alpha	Ppp1ca	cancer type 2 diabetes mellitus
24669	protein phosphatase 1 catalytic subunit gamma	Ppp1cc	cancer congestive heart failure type 2 diabetes mellitus
24849	triosephosphate isomerase 1	Tpi1	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency
78959	aldo-keto reductase family 1 member A1	Akr1a1	breast cancer lung adenocarcinoma
25685	insulin-like growth factor binding protein 1	Igfbp1	breast cancer diabetic angiopathy
290637	collagen beta(1-O)galactosyltransferase 1	Colgalt1	brain small vessel disease 3
81829	malate dehydrogenase 2	Mdh2	brain ischemia congestive heart failure developmental and epileptic encephalopathy 51 myocardial infarction
79255	activating transcription factor 4	Atf4	borna disease prostate carcinoma pulmonary venoocclusive disease
83507	poly (ADP-ribose) glycohydrolase	Parg	borna disease brain infarction stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
170587	citrate synthase	Cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
310864	mannosidase beta	Manba	beta-mannosidosis
290501	transmembrane O-mannosyltransferase targeting cadherins 4	Tmtc4	autosomal recessive nonsyndromic deafness
64445	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	St3gal3	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
24788	sorbitol dehydrogenase	Sord	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
363464	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
24191	aldolase, fructose-bisphosphate C	Aldoc	autoimmune disease of the nervous system borna disease hepatocellular carcinoma

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