|
591
|
|
|
Protein phosphatase, Mg2+/Mn2+ dependent 1B |
PP2C-beta, PP2C-beta-X, PP2CB, PP2CBETA, PPC2BETAX |
|
|
592
|
|
|
Protein phosphatase, Mg2+/Mn2+ dependent 1G |
PP2CG, PP2CGAMMA, PPP2CG |
|
|
593
|
|
|
Phosphatidylinositol glycan anchor biosynthesis class X |
PIG-X |
|
|
594
|
|
|
Protoporphyrinogen oxidase |
PPO, V290M, VP, VPCO |
Anxiety disorder, Colorectal cancer, Colorectal neoplasms, Homozygous variegate porphyria, Mental depression, Nervous system diseases, Polyneuropathy, Porphyria, Variegate porphyria, Porphyruria, Psychosis |
|
595
|
|
|
PIN2 (TERF1) interacting telomerase inhibitor 1 |
Gno1, LPTL, LPTS, Pxr1 |
|
|
596
|
|
|
Protein phosphatase 1 catalytic subunit beta |
HEL-S-80p, MP, NSLH2, PP-1B, PP1B, PP1beta, PP1c, PPP1CD, PPP1beta |
Aortic coarctation, Arnold-chiari malformation, Brachydactyly, Bundle branch block, Cardiofaciocutaneous syndrome, Congenital epicanthus, Congenital pectus carinatum, Congenital pectus excavatum, Costello syndrome, Craniosynostosis, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Dwarfism, High palate, Hydrocephalus, Hypertrophic cardiomyopathy, Hypoplasia of the optic nerve, Leopard syndrome, Macrocephaly, Macrotia, Mental retardation, Neck webbing, Noonan syndrome, Noonan-like syndrome with loose anagen hair, Patent ductus arteriosus, Patent foramen ovale, Peripheral pulmonary artery stenosis, Posteriorly rotated ear, Pulmonary stenosis, Ventricular septal defectView all (16 more) |
|
597
|
|
|
Protein phosphatase 1 catalytic subunit gamma |
PP-1G, PP1C, PPP1G |
|
|
598
|
|
|
Protein phosphatase 2 regulatory subunit B''gamma |
C14orf10, G4-1, G5pr, GDRM, MEGD, SPGF36 |
Agenesis of corpus callosum, Ankylosing spondylitis, Cholangitis, Crohn disease, Dermatitis, Dwarfism, Hypodontia, Imperforate anus, Posteriorly rotated ear, Psoriasis, Rod-cone dystrophy, Spade-like hand, Teratozoospermia, Ulcerative colitis |
|
599
|
|
|
Protein phosphatase 1 regulatory inhibitor subunit 1A |
I1, IPP1 |
|
|
600
|
|
|
PHIP subunit of CUL4-Ring ligase complex |
BRWD2, CHUJANS, DCAF14, DIDOD, RepID, WDR11, ndrp |
Anxiety disorder, Arachnoid cyst, Astigmatism, Attention deficit hyperactivity disorder, Autism, Behavioral abnormality, Clinodactyly, Colorectal cancer, Congenital epicanthus, Congenital torticollis, Convergence insufficiency, Cryptorchidism, Delayed menarche, Developmental delay, Developmental delay, intellectual disability, obesity, and dysmorphic features, Dysautonomia, Exotropia, Febrile seizures, Hearing loss, Hemangioma, High palate, Hyperopia, Hypothyroidism, Mental retardation, Macrotia, Malocclusion, Mental depression, Micrognathism, Myopia, Hypotonia, Nystagmus, Obesity, Obsessive-compulsive disorder, Posteriorly rotated ear, Pulmonary arterial hypertension, Sjogren`s syndrome, Specific learning disorder, Strabismus, Syndactyly, Synophrys, Trichotillomania, UreteroceleView all (27 more) |
