Genes | GeDiPNet - Gene Disease Pathway & Associations

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10141 to 10150 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
10141	23649	POLA2	DNA polymerase alpha 2, accessory subunit	-	Colorectal cancer, Hyperuricemia, Pancreatic cancer, Telomere syndrome
10142	5423	POLB	DNA polymerase beta	-	Colonic neoplasms, Lymphocytic b-cell leukemia, Urinary bladder neoplasms
10143	5424	POLD1	DNA polymerase delta 1, catalytic subunit	CDC2, CRCS10, IMD120, MDPL, POLD	Atrial fibrillation, Colorectal cancer susceptibility, Colorectal neoplasms, Combined immunodeficiency disease, Deafness, Endometrial neoplasms, Colorectal cancer, Hypogonadism, Immunodeficiency, Intellectual developmental disorder, Lipodystrophy, Micrognathism, Obesity
10144	5425	POLD2	DNA polymerase delta 2, accessory subunit	-	Central nervous system cancer, Glioblastoma, Glioma
10145	10714	POLD3	DNA polymerase delta 3, accessory subunit	IMD122, P66, P68, PPP1R128	Atrial fibrillation, Brain infarction, Cerebral amyloid angiopathy, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Diffuse idiopathic skeletal hyperostosis, Gout, Hearing impairment, Hearing loss, Immunodeficiency, Lewy body disease, Osteoarthritis, Pelvic organ prolapse, Uterine prolapse
10146	5426	POLE	DNA polymerase epsilon, catalytic subunit	CRCS12, FILS, IMAGEI, POLE1	Colorectal cancer susceptibility, Colorectal neoplasms, Constitutional mismatch repair deficiency syndrome, Cystic fibrosis, Desbuquois syndrome, Facial dysmorphism syndrome, Colorectal cancer, Constitutional mismatch repair deficiency, Xfe progeroid syndrome
10147	56655	POLE4	DNA polymerase epsilon 4, accessory subunit	YHHQ1, p12	Skin disease, Venous thromboembolism
10148	5428	POLG	DNA polymerase gamma, catalytic subunit	MDP1, MIRAS, MTDPS4A, MTDPS4B, PEO, POLG1, POLGA, SANDO, SCAE	Spinocerebellar ataxia, Autism, Nonsyndromic intellectual disability, Progressive external ophthalmoplegia, Bipolar disorder, Camptocormia, Cardiomyopathy, Cerebellar ataxia, Charcot-marie-tooth disease, Childhood myocerebrohepatopathy spectrum, Congenital neurologic anomalies, Neonatal convulsions, Vascular dementia, Mitochondrial dna depletion syndrome, Schilder disease View all (23 more)
10149	11232	POLG2	DNA polymerase gamma 2, accessory subunit	HP55, MTDPS16, MTDPS16A, MTDPS16B, MTPOLB, PEOA4, POLB, POLG-BETA, POLGB	Asthma, Progressive external ophthalmoplegia, Mitochondrial dna depletion syndrome, Liver failure, Respiratory system disease, Hereditary spastic paraplegia
10150	125316803	POLGARF	POLG alternative reading frame	ORF-Y, POLG	Autism, Mitochondrial dna depletion syndrome, Intellectual developmental disorder, Mitochondrial disease, Mitochondrial hepatopathy, Polyneuropathy, Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis, Hereditary spastic paraplegia

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