Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
1311 to 1320 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1311
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

1312
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

1313
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

1314
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

1315
Peptidyl-tRNA hydrolase 1 homolog
C9orf115, PTH1
Liver cirrhosis

1316
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 neoplasm

1317
Peptidyl-tRNA hydrolase domain containing 1
C2orf79, NEDPBA
Neurodevelopmental disorder, Liver cirrhosis, Non-specific syndromic intellectual disability, Parkinson disease

1318
PTS
6-pyruvoyltetrahydropterin synthase
PTPS
Hyperphenylalaninemia, Bipolar disorder, Metabolic syndrome

1319
PTTG1 regulator of sister chromatid separation, securin
EAP1, ECRAR, HPTTG, PTTG, TUTR1
Hepatocellular carcinoma, Psoriasis, Scoliosis, Sjogren syndrome

1320
754
PTTG1 interacting protein
C21orf1, C21orf3, PBF, PTTG1IP1
Ankylosing spondylitis, Cholecystolithiasis, Gallstones