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 **176 - 200** of **662** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
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
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
18746	pyruvate kinase, muscle	Pkm	disease of metabolism hypertension
18783	phospholipase A2, group IVA (cytosolic, calcium-dependent)	Pla2g4a	asthma brain ischemia hyperglycemia papilloma polycystic kidney disease transitional cell carcinoma
18950	purine-nucleoside phosphorylase	Pnp	purine nucleoside phosphorylase deficiency purine-pyrimidine metabolic disorder
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
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
19045	protein phosphatase 1 catalytic subunit alpha	Ppp1ca	cancer type 2 diabetes mellitus
19046	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
19047	protein phosphatase 1 catalytic subunit gamma	Ppp1cc	cancer congestive heart failure type 2 diabetes mellitus
19309	muscle glycogen phosphorylase	Pygm	cholestasis glycogen storage disease V
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
19703	renin binding protein	Renbp
19719	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Rfng
19733	regucalcin	Rgn	familial hyperlipidemia hepatocellular carcinoma stomach cancer
19895	ribose 5-phosphate isomerase A	Rpia
20322	sorbitol dehydrogenase	Sord	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
20440	beta galactoside alpha 2,6 sialyltransferase 1	St6gal1	alcohol use disorder high grade glioma
20441	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	St3gal3	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
20442	ST3 beta-galactoside alpha-2,3-sialyltransferase 1	St3gal1
20443	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	St3gal4
20444	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	St3gal2
20445	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	St6galnac1	inflammatory bowel disease
20446	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2	St6galnac2
20447	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	St6galnac3

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