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
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
217734	protein-O-mannosyltransferase 2	Pomt2	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
99011	protein-O-mannosyltransferase 1	Pomt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
74653	protein-O-mannose kinase	Pomk	congenital muscular dystrophy-dystroglycanopathy type A12 hydrocephalus muscular dystrophy-dystroglycanopathy type C12
215494	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
68273	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	Pomgnt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
68304	protein O-glucosyltransferase 3	Poglut3
72050	protein O-glucosyltransferase 2	Poglut2
224143	protein O-glucosyltransferase 1	Poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
80294	protein O-fucosyltransferase 2	Pofut2	Down syndrome
140484	protein O-fucosyltransferase 1	Pofut1	Dowling-Degos disease
18950	purine-nucleoside phosphorylase	Pnp	purine nucleoside phosphorylase deficiency purine-pyrimidine metabolic disorder
54128	phosphomannomutase 2	Pmm2	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congenital disorder of glycosylation
29858	phosphomannomutase 1	Pmm1	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I
26433	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	Plod3	hepatocellular carcinoma hypothyroidism
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
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

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