Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "P"

371 to 380 of 1032 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
371	51247	PAIP2	Poly(A) binding protein interacting protein 2	PAIP-2, PAIP2A	Colorectal cancer, Colorectal neoplasms
372	5125	PCSK5	Proprotein convertase subtilisin/kexin type 5	PC5, PC6, PC6A, SPC6	Bone disease, Congenital exomphalos, Congenital omphalocele, Currarino triad, Diverticular diseases, Heart septal defects, Imperforate anus, Jaw abnormalities, Kidney disease, Leukemia, Lower extremity deformities, Lumbosacral agenesis, Lung diseases, Mouth abnormalities, Sacral agenesis View all (4 more)
373	5126	PCSK2	Proprotein convertase subtilisin/kexin type 2	NEC 2, NEC-2, NEC2, PC2, SPC2	Colorectal cancer, Diabetes mellitus
374	51268	PIPOX	Pipecolic acid and sarcosine oxidase	LPIPOX	Adrenoleukodystrophy, Hyperpipecolic acidemia, Mental depression, Peroxisomal dysfunction, Schizophrenia
375	51294	PCDH12	Protocadherin 12	DMJDS1, VE-cadherin-2, VECAD2	Bipolar disorder, Developmental delay, Epilepsy, Exudative retinopathy, Mental retardation, Microcephaly, Microcephaly, seizures, spasticity, and brain calcifications, Myoclonic seizures, Schizoaffective disorder, Schizophrenia, Spastic quadriplegia
376	5130	PCYT1A	Phosphate cytidylyltransferase 1A, choline	CCTA, CCTalpha, CGL5, CT, CTA, CTPCT, PCYT1, SMDCRD	Astigmatism, Brachydactyly, Cataract, Cone-rod dystrophy, Congenital cerebral hernia, Developmental delay, Dwarfism, Hemiplegia/hemiparesis, Keratoconus, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Myopia, Nyctalopia, Nystagmus View all (8 more)
377	51316	PLAC8	Placenta associated 8	C15, DGIC, PNAS-144, onzin	Liver carcinoma
378	51317	PHF21A	PHD finger protein 21A	BHC80, BM-006, IDDBCS, NEDMS	11p11.2 deletion syndrome, Anemia, Brachycephaly, Congenital epicanthus, Defect of skull ossification, Developmental delay, Hypertension, Hypothyroidism, Mental retardation, Micrognathism, Nephroblastoma, Nystagmus, Ovarian epithelial carcinoma, Parietal foramina, Peeling skin syndrome View all (4 more)
379	5133	PDCD1	Programmed cell death 1	ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2, hPD-1, hPD-l, hSLE1	Central nervous system demyelination, Lupus erythematosus, Melanoma, Mental depression, Mood swings, Multiple sclerosis, Nonbacterial verrucal endocardiosis, Systemic lupus erythematosus
380	51334	PRR16	Proline rich 16	DSC54, LARGEN	Mental depression, Mood disorder

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