Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9661 to 9670 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9661
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

9662
Peroxisomal trans-2-enoyl-CoA reductase
DCRRP, HPDHASE, HSA250303, PVIARL, SDR29C1, TERP
Intellectual developmental disorder, Neurodevelopmental disorder

9663
Penta-EF-hand domain containing 1
ABP32, PEF1A
Attention deficit hyperactivity disorder, Autism

9664
Paternally expressed 10
EDR, HB-1, MEF3L, Mar2, Mart2, RGAG3, RTL2, SIRH1
Insomnia

9665
Paternally expressed 3
PW1, ZKSCAN22, ZNF904, ZSCAN24
Central nervous system cancer, Cholangiocarcinoma, Liver disease

9666
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

9667
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

9668
Pellino E3 ubiquitin protein ligase family member 3
-
Insomnia

9669
Pelota mRNA surveillance and ribosome rescue factor
CGI-17, PRO1770
Hearing loss, Diabetes mellitus type 2

9670
Proline, glutamate and leucine rich protein 1
MNAR, P160
Global developmental delay, Psoriasis