|
911
|
|
|
PITPNM family member 3 |
ACKR6, CORD5, NIR1, RDGBA3 |
|
|
912
|
|
|
Polyamine modulated factor 1 binding protein 1 |
SPGF31, STAP |
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Chronic bronchitis, Coronary artery disease, Dementia, Dyslexia, Hyperlipidemia, Iga nephropathy, Major depressive disorder, Male infertility acephalic spermatozoa, Metabolic syndrome, Myocardial infarction, Obsessive-compulsive disorder, Psoriasis, Schizophrenia, Specific language disorder, Spermatogenic failure, Tourette syndrome, Diabetes mellitus, type 2, Venous thromboembolismView all (7 more) |
|
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 |
Asthma, Autism, Parkinson disease, Basal cell carcinoma, Bipolar disorder, Breast cancer, Cancer, Cerebellar ataxia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Color vision deficiency, Colorectal cancer, Congenital neurologic anomalies , Melanoma, Developmental regression, Diabetes mellitus, Diverticular disease, Dystonia, Estrogen-receptor negative breast cancer, Global developmental delay, Hallervorden spatz syndrome, Lung cancer, Melanocytic nevus, Metabolic syndrome, Neurodegeneration with brain iron accumulation, Non-organic psychosis, Osteopetrosis and infantile neuroaxonal dystrophy, Ovarian cancer, Ovarian serous carcinoma, Pelvic organ prolapse, Prostate cancer, Psychotic disorders, Schizophrenia, Skin neoplasm, Spastic ataxia, Squamous cell carcinoma, Diabetes mellitus, type 2, Uterine prolapseView all (22 more) |
|
918
|
|
|
Protein phosphatase 1 regulatory inhibitor subunit 1B |
DARPP-32, DARPP32 |
Asthma, Bipolar disorder, Cardiovascular disease, Catalepsy, Bipolar depression, Major depressive disorder, Dyskinesia, Dyslexia, Depression, Metabolic syndrome, Schizophrenia, Diabetes mellitus, type 2 |
|
919
|
|
|
Protein O-mannose kinase |
MDDGA12, MDDGC12, SGK196 |
|
|
920
|
|
|
RNA polymerase III subunit GL |
RPC32HOM, SOFM, flj32422 |
|