611
|
|
|
Pleckstrin homology and RhoGEF domain containing G6 |
ARHGEF46, MyoGEF |
|
612
|
|
|
Protein phosphatase 2 regulatory subunit Bbeta |
B55BETA, PP2AB55BETA, PP2ABBETA, PP2APR55B, PP2APR55BETA, PR2AB55BETA, PR2ABBETA, PR2APR55BETA, PR52B, PR55-BETA, PR55BETA, SCA12 |
Anxiety disorder, Spinocerebellar ataxia, Cerebellar ataxia, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Delusions, Dementia, Dysarthria, Mental depression, Parkinson disease, Schizophrenia, Sensorimotor neuropathy |
613
|
|
|
Prolyl 3-hydroxylase 2 |
LEPREL1, MCVD, MLAT4 |
|
614
|
|
|
Protein phosphatase 2 regulatory subunit Bgamma |
B55-GAMMA, B55gamma, IMYPNO, IMYPNO1, PR52, PR55G |
|
615
|
|
|
Pantothenate kinase 4 (inactive) |
CTRCT49 |
|
616
|
|
|
Protein phosphatase 2 regulatory subunit B''alpha |
PPP2R3, PR130, PR72 |
|
617
|
|
|
Protein phosphatase 2 phosphatase activator |
PARK25, PP2A, PPP2R4, PR53 |
|
618
|
|
|
Proton activated chloride channel 1 |
ASOR, C1orf75, PAC, PAORAC, TMEM206, hPAC, hTMEM206 |
|
619
|
|
|
Protein phosphatase 2 regulatory subunit B'gamma |
B56G, B56gamma, HJS4, PR61G |
|
620
|
|
|
Protein phosphatase 2 regulatory subunit B'delta |
B56D, B56delta, HJS1, MRD35 |
Autism spectrum disorder, Developmental dysplasia of the hip, Congenital torticollis, Developmental delay, Dysmorphic features, Hydrocephalus, Hypoglycemia, Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome, Macrocephaly, Mental retardation, Myopia, Neurodevelopmental disorders, Speech delay, Strabismus |