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
9701 to 9710 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9701
Phosphatidylethanolamine binding protein 4
CORK-1, CORK1, GWTM1933, HEL-S-300, PEBP-4, PRO4408, hPEBP4
Basal cell carcinoma, Bipolar disorder, Prostate cancer, Retinopathy

9702
Platelet and endothelial cell adhesion molecule 1
CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM
Alzheimer disease, Ankylosing spondylitis, Psoriatic arthritis, Autism, Autoimmune disease, Ischemic heart disease, Coronary artery disease, Coronary stenosis, Myocardial infarction, Myocardial ischemia, Thrombocytopenia

9703
Peroxisomal trans-2-enoyl-CoA reductase
DCRRP, HPDHASE, HSA250303, PVIARL, SDR29C1, TERP
Intellectual developmental disorder, Neurodevelopmental disorder

9704
Penta-EF-hand domain containing 1
ABP32, PEF1A
Attention deficit hyperactivity disorder, Autism

9705
Paternally expressed 10
EDR, HB-1, MEF3L, Mar2, Mart2, RGAG3, RTL2, SIRH1
Insomnia

9706
Paternally expressed 3
PW1, ZKSCAN22, ZNF904, ZSCAN24
Central nervous system cancer, Cholangiocarcinoma, Liver disease

9707
Pellino E3 ubiquitin protein ligase 1
-
Attention deficit hyperactivity disorder, Autism, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Contact dermatitis, Dermatologic disorder, Insomnia, Major depressive disorder, Kawasaki disease, Neurotic disorder, Skin disease

9708
Pellino E3 ubiquitin protein ligase family member 2
-
Alzheimer disease, Asthma, Basal cell carcinoma, Obstructive asthma, Obstructive pulmonary disease, Dementia, Metabolic syndrome, Obesity, Peripheral arterial disease, Schizophrenia, Diabetes mellitus type 2

9709
Pellino E3 ubiquitin protein ligase family member 3
-
Insomnia

9710
Pelota mRNA surveillance and ribosome rescue factor
CGI-17, PRO1770
Hearing loss, Diabetes mellitus type 2