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 **151 - 175** of **662** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
18783	phospholipase A2, group IVA (cytosolic, calcium-dependent)	Pla2g4a	asthma brain ischemia hyperglycemia papilloma polycystic kidney disease transitional cell carcinoma
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
67078	phosphoglycolate phosphatase	Pgp
56012	phosphoglycerate mutase 2	Pgam2	myoglobinuria
18648	phosphoglycerate mutase 1	Pgam1
18663	phosphoglycerate kinase 2	Pgk2	Parkinson's disease cancer
18655	phosphoglycerate kinase 1	Pgk1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
110208	phosphogluconate dehydrogenase	Pgd
226041	phosphoglucomutase 5	Pgm5
109785	phosphoglucomutase 3	Pgm3	cancer cervical cancer immunodeficiency 23 teratoma
70974	phosphoglucomutase 2-like 1	Pgm2l1
66681	phosphoglucomutase 2	Pgm2
72157	phosphoglucomutase 1	Pgm1	congenital disorder of glycosylation It endometrial cancer teratoma
56421	phosphofructokinase, platelet	Pfkp	disease of metabolism glycogen storage disease
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
74551	phosphoenolpyruvate carboxykinase 2 (mitochondrial)	Pck2
18534	phosphoenolpyruvate carboxykinase 1, cytosolic	Pck1	Alzheimer's disease metabolic dysfunction-associated steatohepatitis 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
239827	phosphatidylinositol glycan anchor biosynthesis, class Z	Pigz	cancer
230801	phosphatidylinositol glycan anchor biosynthesis, class V	Pigv	hyperphosphatasia with impaired intellectual development syndrome 1
56176	phosphatidylinositol glycan anchor biosynthesis, class P	Pigp	developmental and epileptic encephalopathy 55
67556	phosphatidylinositol glycan anchor biosynthesis, class M	Pigm
55981	phosphatidylinositol glycan anchor biosynthesis, class B	Pigb	developmental and epileptic encephalopathy 80 sleeping sickness
18700	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria

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