Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "P"

681 to 690 of 1361 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
681	440503	PLIN5	Perilipin 5	LSDA5, LSDP5, MLDP, OXPAT	Alzheimer disease
682	5347	PLK1	Polo like kinase 1	PLK, STPK13	Hepatocellular carcinoma, Glioma, Leukemia, Trichothiodystrophy
683	10769	PLK2	Polo like kinase 2	SNK, hPlk2, hSNK	Alzheimer disease, Juvenile arthritis, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Breast cancer, Carcinoma, Central nervous system cancer, Esophageal adenocarcinoma, Esophageal atresia, Glioblastoma, Glioma, Juvenile idiopathic arthritis, Major depressive disorder, Metabolic syndrome View all (5 more)
684	10733	PLK4	Polo like kinase 4	MCCRP2, SAK, STK18	Chorioretinopathy with microcephaly, Desbuquois syndrome, Dwarfism, Eye disease, Microcephaly, Optic atrophy, Retinitis pigmentosa, Seckel syndrome
685	51090	PLLP	Plasmolipin	PMLP, TM4SF11	Mesothelioma, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2
686	5350	PLN	Phospholamban	CMD1P, CMH18, PLB	Cardiac arrhythmias, Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Cardiac arrest, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Myocardial infarction, Ventricular dysfunction
687	5351	PLOD1	Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1	EDS6, EDSKCL1, LH, LH1, LLH, PLOD	Alzheimer disease, Byzanthine arch palate, Congenital contractural arachnodactyly, Congenital omphalocele, Deep vein thrombosis, Desbuquois syndrome, Ehlers-danlos syndrome, Thoracic aortic aneurysm and aortic dissection, Hydrocephalus, Keratoconus, Mitral valve prolapse, Moyamoya disease, Myopathy, Osteoarthritis, Psoriasis, Psoriasis vulgaris View all (1 more)
688	5352	PLOD2	Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2	BRKS2, LH2, TLH	Juvenile arthritis, Bone fragility with contractures, arterial rupture, and deafness, Bone neoplasms, Bowed long bones, Bruck syndrome, Buruli ulcer, Cleft palate, Congenital camptodactyly, Congenital clubfoot, Congenital hypoplasia of femur, Desbuquois syndrome, Juvenile idiopathic arthritis, Liver cirrhosis, Obesity, Osteoarthritis View all (4 more)
689	8985	PLOD3	Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3	BCARD, LH3	Bone fragility with contractures, arterial rupture, and deafness, Cerebral amyloid angiopathy, Connective tissue disease, Larsen syndrome, Marshall syndrome, Osteoporosis-pseudoglioma syndrome
690	5354	PLP1	Proteolipid protein 1	GPM6C, HLD1, MMPL, PLP, PLP/DM20, PMD, SPG2	Auditory neuropathy, Intellectual developmental disorder, Pelizaeus-merzbacher disease, Schizophrenia, Spastic paraplegia, x-linked, Spastic paraplegia, Hereditary spastic paraplegia

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