Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "P"
1301 to 1310 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1301
Protein tyrosine phosphatase receptor type O
GLEPP1, NPHS6, PTP-OC, PTP-U2, PTPROT, PTPU2, R-PTP-O
Alzheimer disease, Antiphospholipid syndrome, Attention deficit hyperactivity disorder, Autism, Coronary artery disease, Endometriosis, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Gastroesophageal reflux disease, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Hyperopia, Liver neoplasms, Melanoma, Nephrotic syndrome
View all (1 more)

1302
Protein tyrosine phosphatase receptor type Q
DFNA73, DFNB84, DFNB84A, PTPGMC1, R-PTP-Q
Isolated sensorineural deafness, Nonsyndromic hearing loss, Nonsyndromic intellectual disability, Congenital ear anomaly, Congenital pes cavus, Deafness, Hearing impairment, Hearing loss, Pericarditis, Pericardium disorder, Diabetes mellitus type 2

1303
Protein tyrosine phosphatase receptor type R
EC-PTP, PCPTP1, PTP-SL, PTPBR7, PTPRQ
Atrial fibrillation, Central nervous system cancer, Colorectal cancer, Glioblastoma, Glioma, Major depressive disorder, Metabolic syndrome, Osteonecrosis, Schizophrenia, Scoliosis, Diabetes mellitus type 2, Depression, Uterine fibroid

1304
Protein tyrosine phosphatase receptor type S
PTP-sigma, PTPSIGMA, R-PTP-S, R-PTP-sigma
Alzheimer disease, Atrial fibrillation, Dementia, Hearing impairment, Insomnia, Colorectal adenoma, Diabetes mellitus type 2

1305
Protein tyrosine phosphatase receptor type T
R-PTP-T, RPTP-rho, RPTPrho
Anxiety disorder, Asthma, Autism, Breast cancer, Color vision deficiency, Gastroesophageal reflux disease, Intellectual developmental disorder, Major depressive disorder, Periodontitis, Schizophrenia, Venous thromboembolism

1306
Protein tyrosine phosphatase receptor type U
FMI, PCP-2, PTP, PTP-J, PTP-PI, PTP-RO, PTPPSI, PTPRO, PTPU2, R-PTP-PSI, R-PTP-U, hPTP-J
Tourette syndrome

1307
Protein tyrosine phosphatase receptor type Z1
HPTPZ, HPTPzeta, PTP-ZETA, PTP18, PTPRZ, PTPZ, R-PTP-zeta-2, RPTPB, RPTPbeta, phosphacan
Dementia, Ovarian epithelial cancer, Ovarian cancer, Schizophrenia, Myopia

1308
Peptidyl-tRNA hydrolase 2
BIT1, CFAP37, CGI-147, IMNEPD, PTH, PTH 2, PTH2
Cerebellar ataxia, Charcot-marie-tooth disease, Global developmental delay, Hearing impairment, Prostatic neoplasms

1309
Peptidyl-tRNA hydrolase domain containing 1
C2orf79, NEDPBA
Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Parkinson disease

1310
6-pyruvoyltetrahydropterin synthase
PTPS
Hyperphenylalaninemia, Bipolar disorder, Metabolic syndrome