Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9921 to 9930 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9921
PITPNM family member 3
ACKR6, CORD5, NIR1, RDGBA3
Cerebral arteriovenous malformations, Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Cone dystrophy, Cone-rod dystrophy, Metabolic syndrome, Retinitis pigmentosa, Substance abuse, Diabetes mellitus type 2

9922
Pitrilysin metallopeptidase 1
MP1, PreP, SCAR30
Cerebellar ataxia, Spinocerebellar ataxia

9923
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

9924
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)

9925
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)

9926
Piwi like RNA-mediated gene silencing 1
CT80.1, HIWI, MIWI, PIWI
Alzheimer disease, Dementia, Male infertility, Metabolic syndrome

9927
Piwi like RNA-mediated gene silencing 2
CT80, HILI, PIWIL1L, mili
Celiac disease, Male infertility, Male infertility single gene azoospermia, Paralytic strabismus

9928
Piwi like RNA-mediated gene silencing 3
HIWI3
Colorectal cancer

9929
Piwi like RNA-mediated gene silencing 4
HIWI2, MIWI2
Attention deficit hyperactivity disorder, Color vision deficiency, Colorectal cancer, Small cell lung carcinoma

9930
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