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
10351 to 10360 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

10351
PR/SET domain 15
C21orf83, PFM15, ZNF298
Breast cancer, Obstructive pulmonary disease, Insomnia, Parkinson disease, Diabetes mellitus type 2, Venous thromboembolism

10352
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
View all (16 more)

10353
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

10354
PR/SET domain 4
PFM1
Androgenetic alopecia, Digestive system disease, Osteoarthritis

10355
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

10356
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

10357
PR/SET domain 7
PFM4, ZNF910
Color vision deficiency

10358
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)

10359
PR/SET domain 9
KMT8B, MEISETZ, MSBP3, PFM6, ZNF899
Alzheimer disease, Conotruncal cardiac defect, Huntington disease

10360
Peroxiredoxin 1
MSP23, NKEF-A, NKEFA, PAG, PAGA, PAGB, PRX1, PRXI, TDPX2
Asbestosis, Breast cancer, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Obstructive pulmonary disease, Cobalamin c disease, Esophageal neoplasms, Esophageal squamous cell carcinoma, Liver neoplasms, Lung neoplasms, Methylmalonic acidemia