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"
741 to 750 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

741
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)

742
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

743
Pregnancy up-regulated nonubiquitous CaM kinase
BSTK3, CaMK1b
Internet addiction disorder

744
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

745
Polynucleotide kinase 3'-phosphatase
AOA4, CMT2B2, EIEE10, MCSZ, PNK
Ataxia with oculomotor apraxia, Cerebellar atrophy, Charcot-marie-tooth disease, Congenital microcephaly, Congenital neurologic anomalies, Developmental and epileptic encephalopathy, Developmental disability, Dna repair-deficiency disorders, Pyridoxine dependent epilepsy, Global developmental delay, Gout, Heart failure, Intellectual developmental disorder, Microcephaly, Seizures

746
PARN like ribonuclease domain containing exonuclease 1
HsPNLDC1, SPGF57, Trimmer
Coronary artery disease, Male infertility, Male infertility single gene azoospermia, Myocardial infarction, Spermatogenic failure, Testicular azoospermia

747
Pancreatic lipase
PL, PNLIPD, PTL
Pancreatic lipase deficiency

748
Pancreatic lipase related protein 1
PLRP1
Alzheimer disease, Glaucoma, Oligodendroglioma

749
Pancreatic lipase related protein 2 (gene/pseudogene)
PLRP2
Alzheimer disease, Coronary artery disease

750
PNMA family member 1
MA1
Basal cell carcinoma