Detailed description page of humcfs

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EPHX3 details
Primary information
gene_nameEPHX3
Humcfs IdHumcfs_4911
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000105131
havana_transcript_idOTTHUMT00000465798
gene_location15226925-15233435
gene_orientation-
exon_idENSE00003130066, ENSE00000689084, ENSE00000689083, ENSE00000689082, ENSE00000689081, ENSE00000689080, ENSE00001746576, ENSE00003039535, ENSE00003043866
exon_number9
gene_descriptionepoxide hydrolase 3
disease_descriptionSpinocerebellar Ataxia Type 1,Cholangiocarcinoma,Toxoplasmosis,Charcot-Marie-Tooth Disease,Meningioma,Prostate carcinoma,Malignant neoplasm of lung,Meningioma, benign, no ICD-O subtype,Fibroid Tumor,Malignant neoplasm of breast,Atrial Septal Defects,Breast Carcinoma,Stomach Neoplasms,melanoma,Malignant neoplasm of prostate,Carcinoma of lung,Amyotrophic Lateral Sclerosis,Renal Cell Carcinoma,Renal carcinoma,Virus Diseases,Encephalopathies,Alzheimer's Disease,Diabetes,DNA Damage,Acquired CJD,Liver carcinoma,AMYOTROPHIC LATERAL SCLEROSIS 1,Carcinogenesis,Prostatic Neoplasms,Creutzfeldt-Jakob Disease, Sporadic,Neurofibromatosis 2,New Variant Creutzfeldt-Jakob Disease,Neurodegenerative Disorders,Diabetes Mellitus,Obesity,Prion Diseases,Amyotrophic Lateral Sclerosis, Sporadic,Adenomatous Polyposis Coli,Creutzfeldt-Jakob disease,Glioma,Astrocytoma,Bipolar Disorder,Neurofibrillary degeneration (morphologic abnormality),Schizophrenia,Tauopathies,Tuberous Sclerosis,Sarcoma,Uterine Fibroids,Ataxi
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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