Detailed description page of humcfs

This page displays user query in tabular form.

DNM2 details
Primary information
gene_nameDNM2
Humcfs IdHumcfs_4897
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000079805
havana_transcript_idOTTHUMT00000452594
gene_location10718561-10777154
gene_orientation+
exon_idENSE00002789402, ENSE00003541284, ENSE00003632147, ENSE00003587121, ENSE00002957105
exon_number5
gene_descriptiondynamin 2
disease_descriptionCHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder),Congenital Abnormality,Duchenne and Becker Muscular Dystrophy,Cervix carcinoma,Keratoderma, Palmoplantar, Epidermolytic,POLYCYSTIC KIDNEY DISEASE 1,Myopathy,HIV Infections,Bilateral cataracts (disorder),Long QT Syndrome,Coronary heart disease,LETHAL CONGENITAL CONTRACTURE SYNDROME 5,Amyotrophic Lateral Sclerosis,Congenital kyphoscoliosis,Mammary Neoplasms,CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder),Malignant tumor of colon,Axonal neuropathy,Neurodegenerative Disorders,Diabetes Mellitus,Inherited Peripheral Neuropathy,Astrocytoma,Kyphoscoliosis deformity of spine,Alzheimer Disease, Late Onset,X-linked centronuclear myopathy,Akinesia,Mixed sensory-motor polyneuropathy,Tumor Progression,Congenital myopathy (disorder),Prostate carcinoma,Congenital Structural Myopathy,Neutropenia,Boomerang dysplasia,Malignant neoplasm of breast,Breast Carcinoma,Torticollis,Adenoma,Alzheimer's Disease,Ptosis,Leukopenia,Metabolic Dise
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank