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"
561 to 570 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

561
Paired like homeodomain 1
BFT, CCF, LBNBG, POTX, PTX1
Atrial fibrillation, Autism, Brachydactyly-elbow wrist dysplasia syndrome, Hepatocellular carcinoma, Clubfoot, Congenital clubfoot, Desbuquois syndrome, Micrognathism, Pfaundler-hurler syndrome, Testicular carcinoma, Testicular germ cell tumor

562
Paired like homeodomain 2
ARP1, ASGD4, Brx1, IDG2, IGDS, IGDS2, IHG2, IRID2, Otlx2, PTX2, RGS, RIEG, RIEG1, RS
Aniridia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Ataxia with deafness and vision loss, Atrial fibrillation, Atrial flutter, Axenfeld anomaly, Axenfeld-rieger syndrome, Blood coagulation disorder, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Cardiovascular disease, Cataract
View all (19 more)

563
Paired like homeodomain 3
ASGD1, ASMD, ASOD, CTPP4, CTRCT11, PTX3
Alzheimer disease, Anhedonia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Atrial fibrillation, Cataract, Cataract-glaucoma syndrome, Congenital cataract, Congenital cataract anterior segment dysgenesis syndrome, Major depressive disorder, Posterior polar cataract, Microphthalmos, Posterior subcapsular cataract, Prostatic neoplasms
View all (1 more)

564
Piwi like RNA-mediated gene silencing 1
CT80.1, HIWI, MIWI, PIWI
Alzheimer disease, Dementia, Male infertility, Metabolic syndrome

565
Piwi like RNA-mediated gene silencing 2
CT80, HILI, PIWIL1L, mili
Celiac disease, Male infertility, Male infertility single gene azoospermia, Paralytic strabismus

566
Piwi like RNA-mediated gene silencing 3
HIWI3
Colorectal cancer

567
Piwi like RNA-mediated gene silencing 4
HIWI2, MIWI2
Attention deficit hyperactivity disorder, Color vision deficiency, Colorectal cancer, Small cell lung carcinoma

568
Praja ring finger ubiquitin ligase 1
PRAJA1, RNF70
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Craniofrontonasal dysplasia, Major depressive disorder, Parkinson disease, Psychiatric disorders, Schizophrenia

569
Praja ring finger ubiquitin ligase 2
Neurodap1, RNF131
Dupuytren contracture, Frontotemporal dementia, Nasal disorder, Psoriasis

570
Pejvakin
DFNB59
Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss