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 **501 - 525** of **662** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
140484	protein O-fucosyltransferase 1	Pofut1	Dowling-Degos disease
80294	protein O-fucosyltransferase 2	Pofut2	Down syndrome
224143	protein O-glucosyltransferase 1	Poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
72050	protein O-glucosyltransferase 2	Poglut2
68304	protein O-glucosyltransferase 3	Poglut3
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
215494	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
74653	protein-O-mannose kinase	Pomk	congenital muscular dystrophy-dystroglycanopathy type A12 hydrocephalus muscular dystrophy-dystroglycanopathy type C12
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
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
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
231327	phosphoribosyl pyrophosphate amidotransferase	Ppat	hepatocellular carcinoma renal cell carcinoma
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
58200	protein phosphatase 1, regulatory inhibitor subunit 1A	Ppp1r1a
66849	protein phosphatase 1, regulatory inhibitor subunit 2	Ppp1r2
140491	protein phosphatase 1, regulatory subunit 3A	Ppp1r3a	hypoglycemia type 2 diabetes mellitus
244416	protein phosphatase 1, regulatory subunit 3B	Ppp1r3b	alcohol use disorder
53412	protein phosphatase 1, regulatory subunit 3C	Ppp1r3c	alcohol use disorder type 2 diabetes mellitus
76487	protein phosphatase 1, regulatory subunit 3G	Ppp1r3g
68734	protein phosphatase 4 regulatory subunit 3A	Ppp4r3a
104570	protein phosphatase 4 regulatory subunit 3B	Ppp4r3b
105787	protein kinase, AMP-activated, alpha 1 catalytic subunit	Prkaa1	Huntington's disease Parkinson's disease breast cancer cholestasis colon cancer lung non-small cell carcinoma obesity type 2 diabetes mellitus

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