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"
981 to 990 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

981
PR/SET domain 13
CDIDHH, MU-MB-20.220, PCH17, PFM10
Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism, Congenital pontocerebellar hypoplasia, Pontocerebellar hypoplasia, Retinitis pigmentosa

982
PR/SET domain 14
PFM11
Schizophrenia, Testicular carcinoma, Testicular germ cell tumor, Diabetes mellitus type 2

983
PR/SET domain 15
C21orf83, PFM15, ZNF298
Breast cancer, Obstructive pulmonary disease, Insomnia, Parkinson disease, Diabetes mellitus type 2, Venous thromboembolism

984
PR/SET domain 16
CMD1LL, KMT8F, LVNC8, MEL1, PFM13
1p36 deletion syndrome, Asthma, Dilated cardiomyopathy, Cardiomyopathy, Cardiovascular disease, Cerebellar dysfunction with variable cognitive and behavioral abnormalities, Chromosome 1p36 deletion syndrome, Ischemic heart disease, Color vision deficiency, Coronary artery disease, Restrictive cardiomyopathy, Glaucoma, Hypertension, Left ventricular disease, Left ventricular noncompaction cardiomyopathy
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985
PR/SET domain 2
HUMHOXY1, KMT8, KMT8A, MTB-ZF, RIZ, RIZ1, RIZ2
Amphetamine or sympathomimetic abuse, Brain aneurysm, Osteoarthritis, Schizophrenia, Thyroid neoplasms, Urinary bladder neoplasms

986
PR/SET domain 4
PFM1
Androgenetic alopecia, Digestive system disease, Osteoarthritis

987
PR/SET domain 5
BCS2, PFM2
Aortic disease, Astrocytoma, Atrial fibrillation, Axenfeld-rieger syndrome, Brittle cornea syndrome, Connective tissue disease, Ehlers-danlos syndrome, Migraine, Obesity, Osteoarthritis, Diabetes mellitus type 2

988
PR/SET domain 6
KMT8C, PDA3, PRISM
Androgenetic alopecia, Atrial fibrillation, Breast cancer, Cardiovascular disease, Coronary artery disease, Ductus arteriosus, patent, Hypertension, Lung cancer, Metabolic syndrome, Obesity, Patent ductus arteriosus, Prostate cancer, Diabetes mellitus type 2

989
PR/SET domain 7
PFM4, ZNF910
Color vision deficiency

990
PR/SET domain 8
EPM10, KMT8D, PFM5
Androgenetic alopecia, Atrial fibrillation, Atrial flutter, Cardiac arrhythmia, Cardioembolic stroke, Cardiovascular disease, Kidney disease, Coronary artery disease, Lafora body disease, Progressive myoclonic epilepsy with intracellular inclusions, Hypertension, Gout, Heart failure, Hypertensive heart disease, Kidney failure
View all (5 more)