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
10301 to 10310 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10301
PR/SET domain 11
PFM8
Asthma, Atrial fibrillation, Central nervous system cancer, Obstructive pulmonary disease, Erectile dysfunction, Glioblastoma, Glioma, Hyperthyroidism, Hypothyroidism, Major depressive disorder, Meniere disease, Multinodular goiter, Neurotic disorder, Toxic nodular goiter

10302
PR/SET domain 12
HSAN8, PFM9
Congenital insensitivity to pain, Congenital pain insensitivity, Hereditary sensory and autonomic neuropathy

10303
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

10304
PR/SET domain 14
PFM11
Schizophrenia, Testicular carcinoma, Testicular germ cell tumor, Diabetes mellitus type 2

10305
PR/SET domain 15
C21orf83, PFM15, ZNF298
Breast cancer, Obstructive pulmonary disease, Insomnia, Parkinson disease, Diabetes mellitus type 2, Venous thromboembolism

10306
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)

10307
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

10308
PR/SET domain 4
PFM1
Androgenetic alopecia, Digestive system disease, Osteoarthritis

10309
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

10310
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