|
421
|
|
|
RNA polymerase III subunit K |
C11, C11-RNP3, HLD21, My010, RPC10, RPC11, RPC12.5 |
|
|
422
|
|
|
Prodynorphin |
ADCA, PENKB, SCA23 |
Amnesia, Ballismus, Bipolar disorder, Central nervous system demyelination, Cerebellar ataxia, Cerebellar atrophy, Cholestasis, Clonic seizures, Dysarthria, Dyskinesia, Dyskinetic syndrome, Hemiballismus, Hypotonic seizures, Jacksonian seizure, Orofacial dyskinesia, Mental depression, Mood disorder, Movement disorders, Oral dyskinesia, Parkinson disease, Parkinsonian disease, Polyneuropathy, Ramsay hunt paralysis syndrome, Respiration disorders, Respiratory failure, Schizophrenia, Seizure, Sensation disorders, Sensorimotor neuropathy, Sensory disorders, Spinocerebellar ataxia, Status marmoratusView all (17 more) |
|
423
|
|
|
PDZ domain containing 1 |
CAP70, CLAMP, NHERF-3, NHERF3, PDZD1 |
Adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Gout, Gouty arthritis, Marfan syndrome, Prostatic neoplasms, Prostate cancer, Salivary gland neoplasm, Malignant neoplasm of salivary gland, Schizophrenia |
|
424
|
|
|
Platelet and endothelial cell adhesion molecule 1 |
CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM |
|
|
425
|
|
|
Paternally expressed 3 |
PW1, ZKSCAN22, ZNF904, ZSCAN24 |
|
|
426
|
|
|
Proenkephalin |
PE, PENK-A |
|
|
427
|
|
|
Phosphorylated adaptor for RNA export |
RNUXA |
|
|
428
|
|
|
Peptidase D |
PROLIDASE |
Anemia, Arachnodactyly, Asthma, Crusting erythematous dermatitis, Cystitis, Deficiency of prolidase, Developmental delay, Diabetes mellitus, Lung diseases, Lupus erythematosus, Mental retardation, Micrognathism, Palmoplantar keratoderma, Panic disorder, Prolidase deficiency, Proptosis, Ptosis, Respiratory tract diseases, SchizophreniaView all (4 more) |
|
429
|
|
|
Period circadian regulator 1 |
PER, RIGUI, hPER |
|
|
430
|
|
|
Peroxisomal biogenesis factor 1 |
HMLR1, PBD1A, PBD1B, ZWS, ZWS1 |
Acanthosis nigricans, Cubitus valgus, Addison`s disease, Adrenoleukodystrophy, Amelogenesis imperfecta, Cardiomyopathy, Cataract, Cirrhosis, Congenital clubfoot, Congenital epicanthus, Pulmonary hypoplasia, Cryptorchidism, Cystoid macular retinal degeneration, Deafness enamel hypoplasia nail defects, Dental enamel hypoplasia, Developmental delay, Developmental regression, Diabetes mellitus, Dolichocephaly, Dwarfism, Exotropia, Facial paralysis, Glaucoma, Hearing loss, Heimler syndrome, High palate, Hydronephrosis, Hyperopia, Hyperoxaluria, Hypertrophy of clitoris, Hypogonadism, Hypoplasia of the optic nerve, Hypospadias, Ichthyosis, Impaired cognition, Infantile refsum disease, Mental retardation, Leukodystrophy, Liver failure, Liver fibrosis, Macrocephaly, Macroglossia, Macular edema, Malabsorption syndrome, Malformation of cortical development, Maternal hypertension, Microcephaly, Micrognathism, Multicystic renal dysplasia, Hypotonia, Neuronal heterotopia, Nyctalopia, Nystagmus, Obsolete peripheral retinopathy, Optic atrophy, Osteochondrodysplasia, Patent ductus arteriosus, Zellweger syndrome, Physiologic amenorrhea, Polymicrogyria, Posterior embryotoxon, Posteriorly rotated ear, Ptosis, Refsum disease, Renal cyst, Retinitis pigmentosa, Rod-cone dystrophy, Sensory neuropathy, Skeletal dysplasia, Strabismus, Taurodontism, Ventricular septal defect, Vertical nystagmus, Vertical talus, Zellweger-like syndromeView all (60 more) |
