|
911
|
|
|
PITPNM family member 3 |
ACKR6, CORD5, NIR1, RDGBA3 |
|
|
912
|
|
|
Polyamine modulated factor 1 binding protein 1 |
SPGF31, STAP |
|
|
913
|
|
|
Pseudouridine synthase 3 |
2610020J05Rik, DEG1, FKSG32, MRT55, NEDMIGS |
|
|
914
|
|
|
Plasmalemma vesicle associated protein |
DIAR10, FELS, PV-1, PV1, gp68 |
|
|
915
|
|
|
Poly(ADP-ribose) polymerase family member 9 |
ARTD9, BAL, BAL1, MGC:7868 |
|
|
916
|
|
|
Phosphatidylinositol-4-phosphate 5-kinase type 1 beta |
MSS4, STM7 |
|
|
917
|
|
|
Phospholipase A2 group VI |
CaI-PLA2, GVI, INAD1, IPLA2-VIA, NBIA2, NBIA2A, NBIA2B, PARK14, PLA2, PNPLA9, iPLA2, iPLA2beta |
Apraxia, Bipolar disorder, Breast carcinoma, Cerebellar atrophy, Cerebellar cortical atrophy, Cerebellar hypoplasia, Cerebral atrophy, Developmental delay, Developmental regression, Dysarthria, Dyslexia, Dysphagia, Dystonia-parkinsonism, Elbow flexion contracture, Flexion contracture of wrist, Focal dystonia, Frontal bossing, Frontotemporal cerebral atrophy, Frontotemporal dementia, Iron deficiency anemia, Karak syndrome, Malignant melanoma of skin, Melanoma, Mental depression, Mental retardation, Micrognathism, Mood swings, Nasopharyngeal carcinoma, Nephropathy with pretibial epidermolysis bullosa and deafness, Neuroaxonal dystrophy, Nevus, Nonorganic psychosis, Nystagmus, Optic atrophy, Paranoia, Parkinson disease, Periventricular leukomalacia, Psychosis, Schizophrenia, Sensorimotor neuropathy, Spastic quadriplegia, StrabismusView all (27 more) |
|
918
|
|
|
Protein phosphatase 1 regulatory inhibitor subunit 1B |
DARPP-32, DARPP32 |
|
|
919
|
|
|
Protein O-mannose kinase |
MDDGA12, MDDGC12, SGK196 |
Absence of septum pellucidum, Agenesis of corpus callosum, Alpha-dystroglycanopathy, Cardiomyopathy, Cataract, Cerebellar hypoplasia, Cobblestone lissencephaly, Congenital coloboma of iris, Congenital hypoplasia of penis, Congenital keratoglobus, Congenital muscular dystrophy, Congenital muscular dystrophy with cerebellar involvement, Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, Congenital ocular coloboma, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Fukuyama type congenital muscular dystrophy, Glaucoma, Hydrocephalus, Hypoplasia of the optic nerve, Impaired cognition, Limb-girdle muscular dystrophy, Limb-girdle muscular dystrophy-dystroglycanopathy, Lung carcinoma, Macrocephaly, Macroglossia, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Motor delay, Muscle eye brain disease, Muscular dystrophy, Muscular dystrophy-dystroglycanopathy, Myopia, Hypotonia, Neuronal heterotopia, Occipital encephalocele, Optic atrophy, Pachygyria, Polymicrogyria, Posteriorly rotated ear, Retinal detachment, Retinal dysplasia, Retinal dystrophy, Scoliosis, Specific learning disorder, Strabismus, Submucosal cleft palate, Syndromic microphthalmia, Walker-warburg congenital muscular dystrophy, Walker-warburg syndromeView all (38 more) |
|
920
|
|
|
RNA polymerase III subunit GL |
RPC32HOM, SOFM, flj32422 |
|
