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
10671 to 10680 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10671
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

10672
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

10673
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

10674
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

10675
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

10676
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

10677
Peptidyl-tRNA hydrolase 1 homolog
C9orf115, PTH1
Liver cirrhosis

10678
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

10679
Peptidyl-tRNA hydrolase domain containing 1
C2orf79, NEDPBA
Neurodevelopmental disorder, Liver cirrhosis, Non-specific syndromic intellectual disability, Parkinson disease

10680
6-pyruvoyltetrahydropterin synthase
PTPS
Hyperphenylalaninemia, Bipolar disorder, Metabolic syndrome