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
10101 to 10110 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10101
Peptidase, mitochondrial processing subunit beta
Beta-MPP, MAS1, MPP11, MPPB, MPPP52, P-52
Hearing loss

10102
PMS1 homolog 1, mismatch repair system component
HNPCC3, MLH2, PMSL1, hPMS1
Lynch syndrome, Dermatomyositis, Polymyositis, Oligodendroglioma, Prostatic neoplasms

10103
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)

10104
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

10105
Pregnancy up-regulated nonubiquitous CaM kinase
BSTK3, CaMK1b
Internet addiction disorder

10106
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

10107
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

10108
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

10109
Pancreatic lipase
PL, PNLIPD, PTL
Pancreatic lipase deficiency

10110
Pancreatic lipase related protein 1
PLRP1
Alzheimer disease, Glaucoma, Oligodendroglioma