Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
831 to 840 of 1032 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

831
Prokineticin 2
BV8, HH4, KAL4, MIT1, PK2
Alzheimer disease, Hyperalgesia, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Major depressive disorder, Male infertility single gene azoospermia, Male infertility spermatogenesis disorder, Mood disorder, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Willis-ekbom disease, Sheehan syndrome
View all (1 more)

832
Pappalysin 2
PAPP-A2, PAPP-E, PAPPE, PLAC3, SSDA
Autism, Central nervous system cancer, Desbuquois syndrome, Myocardial infarction, Scoliosis

833
PBX/knotted 1 homeobox 2
PREP2
Alzheimer disease, Breast cancer, Creutzfeldt-jakob disease, Estrogen-receptor negative breast cancer, Obesity, Prostate cancer, Schizophrenia, Testicular carcinoma, Diabetes mellitus, type 2

834
Piezo type mechanosensitive ion channel component 2
C18orf30, C18orf58, DA3, DA5, DAIPT, FAM38B, FAM38B2, HsT748, HsT771, MWKS
Androgenetic alopecia, Arthrogryposis multiplex congenita, Arthrogryposis with oculomotor limitation and retinal anomalies, Distal arthrogryposis, Carotid artery disease, Central nervous system cancer, Cerebral palsy, Color vision deficiency, Connective tissue disease, Dental caries, Diverticular disease, Gorlin syndrome, Heterotaxy syndrome, Iga nephropathy, Larsen syndrome
View all (9 more)

835
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

836
Phosphorylated CTD interacting factor 1
C20orf67, CAPAM, MT-A70, PPP1R121, hCAPAM, hPCIF1
Metabolic syndrome, Diabetes mellitus, type 2

837
PR/SET domain 16
CMD1LL, KMT8F, LVNC8, MEL1, PFM13
1p36 deletion syndrome, Asthma, Cardiomyopathy, Cardiovascular disease, Cerebellar dysfunction with variable cognitive and behavioral abnormalities, Chromosome 1p36 deletion syndrome, Ischemic heart disease, Color vision deficiency, Coronary artery disease, Dilated cardiomyopathy, Restrictive cardiomyopathy, Glaucoma, Hypertension, Left ventricular disease, Left ventricular noncompaction cardiomyopathy
View all (16 more)

838
PR/SET domain 14
PFM11
Schizophrenia, Testicular carcinoma, Diabetes mellitus, type 2

839
P53 apoptosis effector related to PMP22
EKVP7, KCP1, KRTCAP1, OLMS2, PIGPC1, THW, dJ496H19.1
Bulimia, Erythrokeratodermia variabilis, Greither disease, Olmsted syndrome

840
Prolyl 3-hydroxylase 1
GROS1, LEPRE1, OI8
Bone fragility with contractures, arterial rupture, and deafness, Desbuquois syndrome, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome