Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "P"

231 to 240 of 1032 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
231	25849	PARM1	Prostate androgen-regulated mucin-like protein 1	Cipar1, DKFZP564O0823, PARM-1, WSC4	Nephrotic syndrome
232	25865	PRKD2	Protein kinase D2	HSPC187, PKD2, nPKC-D2	Cholangitis, Diabetes mellitus, Gastric cancer, Lymphocytic leukemia, Lung adenocarcinoma, Multiple sclerosis, Nasopharyngeal carcinoma, Sclerocystic ovaries, Polycystic ovary syndrome, Sclerosing cholangitis
233	25885	POLR1A	RNA polymerase I subunit A	A190, AFDCIN, HLD27, RPA1, RPA190, RPA194, RPO1-4, RPO14	Acrofacial dysostosis, Burn-mckeown syndrome, Choanal atresia, Anotia, Developmental dysplasia of the hip, Dwarfism, Heart septal defects, Hypoplasia of the maxilla, Macrotia, Microcephaly, Micrognathism, Microtia, Patent ductus arteriosus
234	25886	POC1A	POC1 centriolar protein A	PIX2, SOFT, WDR51A	Brachydactyly, Clinodactyly, Dwarfism, Fanconi anemia, Macrocephaly, Malocclusion, Microcephaly, Microtia, Nail diseases, Nail dysplasia, Oligospermia, Pituitary dwarfism, Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis
235	25891	PAMR1	Peptidase domain containing associated with muscle regeneration 1	DKFZP586H2123, FP938, RAMP	Liver carcinoma
236	25894	PLEKHG4	Pleckstrin homology and RhoGEF domain containing G4	ARHGEF44, PRTPHN1, SCA4	Dysarthria, Spinocerebellar ataxia
237	25913	POT1	Protection of telomeres 1	CMM10, CRMCC3, GLM9, HPOT1, PFBMFT8, TPDS3	Anaplastic oligodendroglioma, Astrocytoma, Atypical mole melanoma syndrome, Autosomal chromosome disorders, Lymphocytic leukemia, Mammary neoplasms, Congenital chromosomal disease, Glioma, Leukemia, Lymphoid leukemia, Melanoma, Nevus, Oligodendroglioma, Pancreatic neoplasm, Renal carcinoma View all (4 more)
238	25930	PTPN23	Protein tyrosine phosphatase non-receptor type 23	HD-PTP, HDPTP, NEDBASS, PTP-TD14	Brain atrophy, Developmental delay, Diabetes mellitus, Epilepsy, Mental retardation
239	25953	PNKD	PNKD metallo-beta-lactamase domain containing	BRP17, DYT8, FKSG19, FPD1, KIPP1184, MR-1, MR-1S, MR1, PDC, PKND1, PNKD1, R1, TAHCCP2	Cardiovascular diseases, Choreoathetosis, Chromophobe carcinoma, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Crohn disease, Dysarthria, Dyskinesia, Dyskinetic syndrome, Dysphagia, Inflammatory bowel disease, Papillary renal carcinoma, Paroxysmal nonkinesigenic dyskinesia View all (4 more)
240	25973	PARS2	Prolyl-tRNA synthetase 2, mitochondrial	DEE75, EIEE75, MT-PRORS, proRS	Alpers syndrome, Attention deficit hyperactivity disorder, Autism, Central visual impairment, Cerebral atrophy, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Hypoplasia of corpus callosum, Mental retardation, Microcephaly View all (6 more)

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