GlyCosmos Portal

Rattus norvegicus (Norway rat)

Summary

Taxonomy ID: 10116
PubChem Taxonomy: 10116

Genes (449) Glycans (773) Glycoproteins (2935) Lectins (166) Pathways (1070)

Displaying entries **326 - 350** of **449** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
362518	post-GPI attachment to proteins GalNAc transferase 4	Pgap4
100360180	phosphogluconate dehydrogenase	Pgd
94203	placental growth factor	Pgf	Crohn's disease amyotrophic lateral sclerosis ankylosing spondylitis asthma brain ischemia breast cancer carotid artery disease congestive heart failure diabetic neuropathy diabetic retinopathy end stage renal disease epilepsy glioblastoma hypertension limited scleroderma liver cirrhosis lymphedema myocardial infarction obesity pancreatic endocrine carcinoma pre-eclampsia pulmonary hypertension pyelonephritis renal cell carcinoma rheumatoid arthritis sickle cell anemia status epilepticus systemic lupus erythematosus temporal lobe epilepsy
24644	phosphoglycerate kinase 1	Pgk1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
287115	phosphoglycolate phosphatase	Pgp
29353	phosphorylase kinase catalytic subunit gamma 1	Phkg1
140671	phosphorylase kinase catalytic subunit gamma 2	Phkg2	glycogen storage disease IXc glycogen storage disease liver cirrhosis
363464	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
315807	phosphatidylinositol glycan anchor biosynthesis, class B	Pigb	developmental and epileptic encephalopathy 80 sleeping sickness
79112	phosphatidylinositol glycan anchor biosynthesis, class M	Pigm
366478	phosphatidylinositol glycan anchor biosynthesis, class V	Pigv	hyperphosphatasia with impaired intellectual development syndrome 1
303872	phosphatidylinositol glycan anchor biosynthesis, class Z	Pigz	cancer
170911	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
25513	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
24651	pyruvate kinase L/R	Pklr	Gaucher's disease congenital nonspherocytic hemolytic anemia disease of metabolism hyperglycemia malaria metabolic dysfunction-associated steatotic liver disease pyruvate kinase deficiency of red cells type 2 diabetes mellitus
25630	pyruvate kinase M1/2	Pkm	disease of metabolism hypertension
288583	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	Plod3	hepatocellular carcinoma hypothyroidism
311551	protein O-fucosyltransferase 1	Pofut1	Dowling-Degos disease
309686	protein O-fucosyltransferase 2	Pofut2	Down syndrome
288091	protein O-glucosyltransferase 1	Poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
315664	protein O-glucosyltransferase 3	Poglut3
362567	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	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
316091	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
306549	protein-O-mannose kinase	Pomk	congenital muscular dystrophy-dystroglycanopathy type A12 hydrocephalus muscular dystrophy-dystroglycanopathy type C12
84430	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

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