Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "P"
731 to 740 of 1369 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

731
PMF1-BGLAP readthrough
PMF-1, PMF1
Breast cancer, Clear cell renal cell carcinoma, Intracerebral hemorrhage, Kidney cancer, Myeloproliferative disorder, Parkinson disease, Small vessel stroke, Stroke

732
Polyamine modulated factor 1 binding protein 1
SPGF31, STAP
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bronchitis, Coronary artery disease, Dementia, Dyslexia, Hyperlipidemia, Iga nephropathy, Major depressive disorder, Male infertility acephalic spermatozoa, Metabolic syndrome, Myocardial infarction, Obsessive-compulsive disorder
View all (8 more)

733
PML nuclear body scaffold
MYL, PP8675, RNF71, TRIM19
Diabetes mellitus, Dyslipidemias, Glioblastoma, Insomnia, Promyelocytic leukemia, Liver neoplasms, Metabolic syndrome, Prostatic neoplasms, Schizophrenia, Stevens-johnson syndrome, Diabetes mellitus type 2, Uterine fibroid

734
Phosphomannomutase 1
PMM 1, PMMH-22, Sec53
Attention deficit hyperactivity disorder, Autism, Global developmental delay

735
Phosphomannomutase 2
CDG1, CDG1a, CDGS, PMI, PMI1, PMM 2
Breast cancer, Cerebellar ataxia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Cerebral atrophy, Cerebral palsy, Colorectal neoplasms, Congenital disorder of glycosylation, Diabetes mellitus, Focal glomerulosclerosis, Hyperinsulinemic hypoglycemia, Intellectual developmental disorder, Muscular dystrophy, Open angle glaucoma, Premature ovarian failure, Pituitary stalk interruption syndrome

736
Peripheral myelin protein 2
CMT1G, FABP8, M-FABP, MP2, P2
Charcot-marie-tooth disease, Cutaneous mastocytosis, Ovarian cancer, Ovarian serous carcinoma, Peripheral neuropathy, Schizophrenia, Diabetes mellitus type 2

737
Peripheral myelin protein 22
CIDP, CMT1A, CMT1E, DSS, GAS-3, GAS3, HMSNIA, HNPP, Sp110
Charcot-marie-tooth disease, Dejerine-sottas disease, Demyelinating diseases, Developmental disability, Distal spinal muscular atrophy, Myoclonic epilepsy, Hereditary motor and sensory neuropathies, Hereditary sensory and motor neuropathy, Hypertrophic neuropathy, Hereditary, neuropathy with liability to pressure palsies, Non-neoplastic peripheral nervous system disease, Paresthesia, Peripheral nervous system disease, Peripheral neuropathy, Peroneal muscle atrophy
View all (3 more)

738
Peptidase, mitochondrial processing subunit alpha
Alpha-MPP, CLA1, CPD3, INPP5E, MAS2, P-55, SCAR2
Cerebelloparenchymal disorder, Spinocerebellar ataxia, Ptosis, Blindness, Cerebellar ataxia, Lactic acidosis, Normal pressure hydrocephalus, Hypertrophic cardiomyopathy, Inflammatory bowel disease, Mitochondrial disease, Optic atrophy

739
Peptidase, mitochondrial processing subunit beta
Beta-MPP, MAS1, MPP11, MPPB, MPPP52, P-52
Hearing loss

740
PMS1 homolog 1, mismatch repair system component
HNPCC3, MLH2, PMSL1, hPMS1
Lynch syndrome, Dermatomyositis, Polymyositis, Oligodendroglioma, Prostatic neoplasms