Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "P"
731 to 740 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

731
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

732
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

733
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)

734
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

735
Peptidase, mitochondrial processing subunit beta
Beta-MPP, MAS1, MPP11, MPPB, MPPP52, P-52
Hearing loss

736
PMS1 homolog 1, mismatch repair system component
HNPCC3, MLH2, PMSL1, hPMS1
Lynch syndrome, Dermatomyositis, Polymyositis, Oligodendroglioma, Prostatic neoplasms

737
PMS1 homolog 2, mismatch repair system component
HNPCC4, LYNCH4, MLH4, MMRCS4, PMS-2, PMS2CL, PMSL2
Breast cancer, Cafe-au-lait spots, Dilated cardiomyopathy, Cardiomyopathy, Lynch syndrome, Colorectal neoplasms, Constitutional mismatch repair deficiency syndrome, Hereditary breast cancer, Pancreatic neoplasms, Constitutional mismatch repair deficiency, Muir-torre syndrome, Ocular sarcoidosis, Ovarian cancer, Prostate cancer, Rhabdomyosarcoma
View all (1 more)

738
Phosphomevalonate kinase
HUMPMKI, PMK, PMKA, PMKASE, POROK1
Atrial fibrillation, Autoinflammatory syndrome, Bipolar disorder, Cardiac embolism, Cardioembolic stroke, Dyslexia, Osteoarthritis, Parkinson disease, Porokeratosis, Prostate cancer, Schizophrenia

739
Pregnancy up-regulated nonubiquitous CaM kinase
BSTK3, CaMK1b
Internet addiction disorder

740
PNKD metallo-beta-lactamase domain containing
BRP17, DYT8, FKSG19, FPD1, KIPP1184, MR-1, MR-1S, MR1, PDC, PKND1, PNKD1, R1, TAHCCP2
Renal cell carcinoma, Cardiovascular disease, Cholecystolithiasis, Colorectal adenoma, Colorectal cancer, Crohn disease, Dyskinesia, Gallstones, Tourette syndrome, Inflammatory bowel disease, Moyamoya angiopathy, Paroxysmal nonkinesigenic dyskinesia, Diabetes mellitus type 2, Ulcerative colitis