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
18207	nth (endonuclease III)-like 1 (E.coli)	Nthl1	familial adenomatous polyposis 3
217166	nuclear receptor subfamily 1, group D, member 1	Nr1d1	alcoholic liver cirrhosis brain small vessel disease hyperthyroidism hypothyroidism portal hypertension type 2 diabetes mellitus
53893	nudix hydrolase 5	Nudt5
15379	one cut domain, family member 1	Onecut1
18419	otogelin	Otog	autosomal recessive nonsyndromic deafness 18B
628870	otogelin-like	Otogl	autosomal recessive nonsyndromic deafness 84B
12659	oviductal glycoprotein 1	Ovgp1
18293	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	Ogdh	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
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
18627	period circadian clock 2	Per2	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
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
18700	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
55981	phosphatidylinositol glycan anchor biosynthesis, class B	Pigb	developmental and epileptic encephalopathy 80 sleeping sickness
67556	phosphatidylinositol glycan anchor biosynthesis, class M	Pigm
56176	phosphatidylinositol glycan anchor biosynthesis, class P	Pigp	developmental and epileptic encephalopathy 55
230801	phosphatidylinositol glycan anchor biosynthesis, class V	Pigv	hyperphosphatasia with impaired intellectual development syndrome 1
239827	phosphatidylinositol glycan anchor biosynthesis, class Z	Pigz	cancer
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
18534	phosphoenolpyruvate carboxykinase 1, cytosolic	Pck1	Alzheimer's disease metabolic dysfunction-associated steatohepatitis type 2 diabetes mellitus
74551	phosphoenolpyruvate carboxykinase 2 (mitochondrial)	Pck2
18641	phosphofructokinase, liver, B-type	Pfkl	disease of metabolism glycogen storage disease
18642	phosphofructokinase, muscle	Pfkm	disease of metabolism glycogen storage disease VII glycogen storage disease
56421	phosphofructokinase, platelet	Pfkp	disease of metabolism glycogen storage disease
72157	phosphoglucomutase 1	Pgm1	congenital disorder of glycosylation It endometrial cancer teratoma

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