Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10051 to 10060 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10051
PML nuclear body scaffold
MYL, PP8675, RNF71, TRIM19
Diabetes mellitus, Dyslipidemias, Glioblastoma, Insomnia, Promyelocytic leukemia, Metabolic syndrome, Prostatic neoplasms, Schizophrenia, Stevens-johnson syndrome, Diabetes mellitus type 2, Uterine fibroid

10052
Phosphomannomutase 1
PMM 1, PMMH-22, Sec53
Attention deficit hyperactivity disorder, Autism, Global developmental delay

10053
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

10054
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

10055
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
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10056
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

10057
Peptidase, mitochondrial processing subunit beta
Beta-MPP, MAS1, MPP11, MPPB, MPPP52, P-52
Hearing loss

10058
PMS1 homolog 1, mismatch repair system component
HNPCC3, MLH2, PMSL1, hPMS1
Lynch syndrome, Dermatomyositis, Polymyositis, Oligodendroglioma, Prostatic neoplasms

10059
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
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10060
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