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 **201 - 225** of **449** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
25134	glycine N-methyltransferase	Gnmt	glycine N-methyltransferase deficiency hepatocellular carcinoma
24401	glutamic-oxaloacetic transaminase 1	Got1	amyloidosis amyotrophic lateral sclerosis cardiomyopathy pancreatic ductal adenocarcinoma transient cerebral ischemia
60666	glycerol-3-phosphate dehydrogenase 1	Gpd1
25062	glycerol-3-phosphate dehydrogenase 2	Gpd2	type 2 diabetes mellitus
292804	glucose-6-phosphate isomerase	Gpi	Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia congenital hemolytic anemia congenital nonspherocytic hemolytic anemia heart disease intellectual disability neuromuscular disease
50686	glycogen synthase kinase 3 alpha	Gsk3a	Parkinsonism amyotrophic lateral sclerosis
84027	glycogen synthase kinase 3 beta	Gsk3b	Alzheimer's disease Parkinson's disease acute myocardial infarction amyotrophic lateral sclerosis bipolar disorder colon cancer colorectal adenocarcinoma degenerative disc disease depressive disorder diabetic encephalopathy endometrial carcinoma heart disease hypertension middle cerebral artery infarction myocardial infarction oral squamous cell carcinoma schizophrenia sciatic neuropathy status epilepticus substance-related disorder type 2 diabetes mellitus vascular dementia
309465	glutathione S-transferase omega 2	Gsto2	Alzheimer's disease Parkinson's disease alcohol use disorder asthma
362129	glycosyltransferase-like domain containing 1	Gtdc1
60671	gulonolactone (L-) oxidase	Gulo
24434	glucuronidase, beta	Gusb	Sly syndrome mucopolysaccharidosis peritonitis
300173	glucoside xylosyltransferase 1	Gxylt1
688618	glucoside xylosyltransferase 2	Gxylt2
81675	glycogenin 1	Gyg1	glycogen storage disease XV glycogen storage disease
690987	glycogen synthase 1	Gys1	Lafora disease cardiovascular system disease
25623	glycogen synthase 2	Gys2	Lafora disease glycogen storage disease
282821	hyaluronan synthase 1	Has1	pulmonary hypertension
25694	hyaluronan synthase 2	Has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
266805	hyaluronan synthase 3	Has3	pulmonary hypertension
300757	hexosaminidase subunit alpha	Hexa	Tay-Sachs disease
294673	hexosaminidase subunit beta	Hexb	Sandhoff disease lysosomal storage disease spinal muscular atrophy
25058	hexokinase 1	Hk1	Charcot-Marie-Tooth disease type 4G acute lymphoblastic leukemia anemia colorectal cancer congenital nonspherocytic hemolytic anemia glucose metabolism disease multiple myeloma obesity pulmonary hypertension retinitis pigmentosa sickle cell anemia urinary bladder cancer
25059	hexokinase 2	Hk2	glucose metabolism disease hypertension obesity type 2 diabetes mellitus
25060	hexokinase 3	Hk3	glucose metabolism disease
25459	high mobility group box 1	Hmgb1	Kawasaki disease amyotrophic lateral sclerosis atherosclerosis brain infarction cerebral infarction colon adenocarcinoma congestive heart failure high grade glioma hydrocephalus middle cerebral artery infarction myocardial infarction obstructive jaundice periodontitis pulmonary hypertension sciatic neuropathy systemic scleroderma

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