GlyCosmos Portal

Mus musculus (house mouse)

Summary

Taxonomy ID: 10090
PubChem Taxonomy: 10090

Genes (662) Glycans (1270) Glycoproteins (13000) Lectins (276) Pathways (1335)

Displaying entries **476 - 500** of **662** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
19662	retinol binding protein 4, plasma	Rbp4	acute pyelonephritis atherosclerosis cerebral infarction chronic kidney disease colon adenoma congestive heart failure coronary artery disease diabetic angiopathy diabetic retinopathy dilated cardiomyopathy essential hypertension familial hypercholesterolemia gallbladder cancer gestational diabetes hyperinsulinism hypertension liver cirrhosis myocardial infarction obesity pre-eclampsia proliferative diabetic retinopathy psoriasis severe pre-eclampsia systemic scleroderma type 2 diabetes mellitus
19309	muscle glycogen phosphorylase	Pygm	cholestasis glycogen storage disease V
19047	protein phosphatase 1 catalytic subunit gamma	Ppp1cc	cancer congestive heart failure type 2 diabetes mellitus
19046	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
19045	protein phosphatase 1 catalytic subunit alpha	Ppp1ca	cancer type 2 diabetes mellitus
19017	peroxisome proliferative activated receptor, gamma, coactivator 1 alpha	Ppargc1a	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome age related macular degeneration amblyopia amyotrophic lateral sclerosis cardiovascular system disease chronic obstructive pulmonary disease colitis congenital hypothyroidism diabetic retinopathy dilated cardiomyopathy heart disease hyperglycemia hyperthyroidism kidney cancer kidney failure macular degeneration malignant fibrous histiocytoma melanoma metabolic dysfunction-associated steatotic liver disease myocardial infarction nephrotic syndrome obesity placental insufficiency prediabetes syndrome primary biliary cholangitis renal fibrosis sciatic neuropathy steatotic liver disease type 2 diabetes mellitus
19013	peroxisome proliferator activated receptor alpha	Ppara	Alzheimer's disease alcoholic hepatitis coronary artery disease cystic fibrosis hepatocellular carcinoma hydrocephalus hypertension hypertensive encephalopathy lipid metabolism disorder myocardial infarction obesity periodontitis schizophrenia steatotic liver disease
18950	purine-nucleoside phosphorylase	Pnp	purine nucleoside phosphorylase deficiency purine-pyrimidine metabolic disorder
18783	phospholipase A2, group IVA (cytosolic, calcium-dependent)	Pla2g4a	asthma brain ischemia hyperglycemia papilloma polycystic kidney disease transitional cell carcinoma
18746	pyruvate kinase, muscle	Pkm	disease of metabolism hypertension
18708	phosphoinositide-3-kinase regulatory subunit 1	Pik3r1	Alzheimer's disease SHORT syndrome X-linked agammaglobulinemia agammaglobulinemia 7 astroblastoma colorectal cancer endometrial adenocarcinoma endometrial cancer endometrial carcinoma hepatocellular carcinoma hypertension immunodeficiency 36 lung adenocarcinoma lung small cell carcinoma obesity osteoarthritis portal hypertension prostate cancer renal cell carcinoma rheumatoid arthritis type 2 diabetes mellitus
18706	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	Pik3ca	CLOVES syndrome Cowden syndrome 5 autosomal recessive polycystic kidney disease breast angiosarcoma breast cancer cerebral cavernous malformation colon adenocarcinoma colorectal cancer colorectal carcinoma cutaneous Paget's disease epidermal nevus esophageal cancer estrogen-receptor positive breast cancer hepatocellular carcinoma lung cancer ovarian cancer rectal benign neoplasm seborrheic keratosis stomach cancer
18700	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
18682	phosphorylase kinase gamma 1	Phkg1
18679	phosphorylase kinase alpha 1	Phka1	glycogen storage disease IXd glycogen storage disease hypothyroidism
18663	phosphoglycerate kinase 2	Pgk2	Parkinson's disease cancer
18655	phosphoglycerate kinase 1	Pgk1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
18654	placental growth factor	Pgf	Crohn's disease amyotrophic lateral sclerosis ankylosing spondylitis asthma brain ischemia breast cancer carotid artery disease congestive heart failure diabetic neuropathy diabetic retinopathy end stage renal disease epilepsy glioblastoma hypertension limited scleroderma liver cirrhosis lymphedema myocardial infarction obesity pancreatic endocrine carcinoma pre-eclampsia pulmonary hypertension pyelonephritis renal cell carcinoma rheumatoid arthritis sickle cell anemia status epilepticus systemic lupus erythematosus temporal lobe epilepsy
18648	phosphoglycerate mutase 1	Pgam1
18642	phosphofructokinase, muscle	Pfkm	disease of metabolism glycogen storage disease VII glycogen storage disease
18641	phosphofructokinase, liver, B-type	Pfkl	disease of metabolism glycogen storage disease
18640	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	Pfkfb2
18639	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1	Pfkfb1	hyperinsulinism
18627	period circadian clock 2	Per2	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
18609	pancreatic and duodenal homeobox 1	Pdx1	acute necrotizing pancreatitis cerebral infarction diabetes mellitus diabetic retinopathy hyperglycemia maturity-onset diabetes of the young type 4 maturity-onset diabetes of the young obesity pancreatic agenesis placental insufficiency type 1 diabetes mellitus type 2 diabetes mellitus

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