Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9481 to 9490 of 15435 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9481
Parvin gamma
-
Colonic neoplasms, Colorectal cancer, Schizophrenia

9482
PAS domain containing serine/threonine kinase
PASKIN, STK37
Autism, Chromosome 2q37 deletion syndrome, Kidney disease

9483
Prostate and testis expressed 3
HEL-127, PATE-DJ
Astrocytoma

9484
Prostate and testis expressed 4
PATE-B
Astrocytoma

9485
PATJ crumbs cell polarity complex component
Cipp, INADL, InaD-like, hINADL
Bell's palsy, Biliary atresia, Insomnia, Metabolic syndrome, Obesity, Oligodendroglioma, Prostatic neoplasms, Scoliosis, Skin disease, Diabetes mellitus type 2

9486
PAT1 homolog 2
OOMD4, OZEMA4, Pat1a, hPat1a
Female infertility, Oocyte maturation defect

9487
Pro-apoptotic WT1 regulator
PAR4, Par-4
Attention deficit hyperactivity disorder, Bladder exstrophy, Conduct disorder, Coronary artery disease, Endometrial neoplasms, Major depressive disorder, Prostatic neoplasms, Psychotic disorders, Schizophrenia, Depression

9488
Paired box 1
HUP48, OFC2, OTFCS2
Branchiootorenal syndrome, Glioma, Goldenhar syndrome, Otofaciocervical syndrome

9489
Paired box 2
FSGS7, PAPRS, PAX-2
Alzheimer disease, Anophthalmia/microphthalmia-esophageal atresia syndrome, Renal hypoplasia, Congenital anomalies of the kidney and urinary tract, Cardiovascular disease, Congenital hypoplasia of kidney, Congenital ocular coloboma, Endometriosis, Idiopathic steroid-resistant nephrotic syndrome, Female infertility, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Gout, Hereditary steroid-resistant nephrotic syndrome
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9490
Paired box 3
CDHS, HUP2, PAX-3, WS1, WS3
Alzheimer disease, Androgenetic alopecia, Asthma, Central precocious puberty, Congenital diaphragmatic hernia, Congenital hand deformities, Congenital neurologic anomalies, Craniofacial abnormalities, Craniofacial deafness hand syndrome, Deafness, Desbuquois syndrome, Hearing impairment, Insomnia, Intellectual developmental disorder, Kleins syndrome
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