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
9421 to 9430 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9421
Par-3 family cell polarity regulator
ASIP, Baz, PAR3, PAR3alpha, PARD-3, PARD3A, PPP1R118, SE2-5L16, SE2-5LT1, SE2-5T2
Autism, Cardiac arrest, Lymphoblastic leukemia, Corneal astigmatism, Emphysema, Major depressive disorder, Neural tube defect, Nonalcoholic fatty liver disease, Oligodendroglioma, Premature ovarian failure, Parkinson disease, Prostatic neoplasms, Willis-ekbom disease

9422
Par-3 family cell polarity regulator beta
ALS2CR19, PAR3B, PAR3L, PAR3beta
Asthma, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Brain aneurysm, Breast cancer, Craniofacial microsomia, Diabetic neuropathy, Dilated cardiomyopathy, Gastric cancer, Hypertrophic cardiomyopathy, Metabolic syndrome, Neurodevelopmental disorder, Ocular sarcoidosis, Open angle glaucoma
View all (7 more)

9423
Par-6 family cell polarity regulator beta
PAR6B
Autism, Basal cell carcinoma, Bipolar disorder, Colorectal cancer, Keratinocyte carcinoma, Non-melanoma skin carcinoma, Psychiatric disorders, Scoliosis, Skin cancer, Skin neoplasms

9424
Par-6 family cell polarity regulator gamma
PAR-6G, PAR6gamma
Alzheimer disease, Osteoarthritis, Schizophrenia

9425
Parkinsonism associated deglycase
DJ-1, DJ1, GATD2, HEL-S-67p
Amyotrophic lateral sclerosis, Ankylosing spondylitis, Parkinson disease, Behcet disease, Hepatocellular carcinoma, Celiac disease, Ischemic stroke, Crohn disease, Inflammatory bowel disease, Motor neuron disease, Osteoporosis, Hereditary parkinson disease, Parkinson-dementia complex of guam, Psoriasis, Sclerosing cholangitis
View all (2 more)

9426
Presenilin associated rhomboid like
PRO2207, PSARL, PSARL1, PSENIP2, RHBDS1
Ischemic heart disease, Coronary artery disease, Diabetes mellitus type 2, Hyperinsulinism, Myocardial ischemia, Myopia, Leber hereditary optic neuropathy

9427
Prostate androgen-regulated mucin-like protein 1
Cipar1, DKFZP564O0823, PARM-1, WSC4
Nephrotic syndrome, Scoliosis

9428
Poly(A)-specific ribonuclease
DAN, DKCB6, PFBMFT4
Alzheimer disease, Dyskeratosis congenita, Hoyeraal hreidarsson syndrome, Idiopathic pulmonary fibrosis, Paralytic strabismus, Psoriasis, Pulmonary fibrosis, Telomere-related pulmonary fibrosis and/or bone marrow failure, Telomere syndrome

9429
Poly(ADP-ribose) polymerase 1
ADPRT, ADPRT 1, ADPRT1, ARTD1, PARP, PARP-1, PARS, PPOL, Poly-PARP, pADPRT-1
Alzheimer disease, Anemia, Ankylosing spondylitis, Aortic aneurysm, Arthritis, Asthma, Atherosclerosis, Brain injuries, Brain ischemia, Breast cancer, Breast neoplasms, Cancer, Hepatocellular carcinoma, Cardiomyopathy, Neuronal ceroid lipofuscinosis
View all (28 more)

9430
Poly(ADP-ribose) polymerase family member 10
ARTD10
Bipolar disorder, Developmental delay, Ulcerative colitis, Venous thromboembolism