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 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

981
Photoreceptor disc component
RP36
Diabetic neuropathy, Retinitis pigmentosa, Squamous cell carcinoma, Diabetes mellitus type 2

982
Prolylcarboxypeptidase
HUMPCP, PCP
Obesity, Scoliosis

983
PR/SET domain 1
BLIMP-1, BLIMP1, PRDI-BF1
Androgenetic alopecia, Ankylosing spondylitis, Experimental arthritis, Rheumatoid arthritis, Ulcerative colitis, Colorectal cancer, Crohn disease, Inflammatory bowel disease, Insomnia, Systemic lupus erythematosus, Psoriasis, Sclerosing cholangitis, Scoliosis, Sjogren syndrome

984
PR/SET domain 10
BHD2, PFM7, TRIS
Birt-hogg-dube syndrome, Central nervous system cancer, Color vision deficiency, Dementia, Glioblastoma, Glioma

985
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

986
PR/SET domain 12
HSAN8, PFM9
Congenital insensitivity to pain, Congenital pain insensitivity, Hereditary sensory and autonomic neuropathy

987
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

988
PR/SET domain 14
PFM11
Schizophrenia, Testicular carcinoma, Testicular germ cell tumor, Diabetes mellitus type 2

989
PR/SET domain 15
C21orf83, PFM15, ZNF298
Breast cancer, Obstructive pulmonary disease, Insomnia, Parkinson disease, Diabetes mellitus type 2, Venous thromboembolism

990
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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