Detailed description page of humcfs

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Humcfs_2158 details
Primary information
Humcfs IdHumcfs_2158
chromosome_numberchromosome7
nameFRA7I
chrlocation147900001-159138663
cytoband7q36
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000130226
gene_nameDPP6
havana_transcript_idOTTHUMT00000322931
gene_location154052418-154588631
gene_orientation+
exon_idENSE00001558896, ENSE00003659278, ENSE00003582120, ENSE00003653234, ENSE00003591401, ENSE00001552531
exon_number6
gene_descriptiondipeptidyl-peptidase 6
disease_descriptionHuntington Disease,Atrial Septal Defects,Child Development Disorders, Pervasive,Autism Spectrum Disorders,EARLY REPOLARIZATION ASSOCIATED WITH VENTRICULAR FIBRILLATION,Attention deficit hyperactivity disorder,Ventricular Fibrillation,Pancreatic Neoplasm,Hypertrophic Cardiomyopathy,Spastic Paraplegia, Hereditary,Leukemia, Myelocytic, Acute,Ventricular Fibrillation, Paroxysmal Familial, 2,Malignant neoplasm of pancreas,Endometriosis,Amyotrophic Lateral Sclerosis, Sporadic,Dyskinetic syndrome,Neuroleptic-Induced Tardive Dyskinesia,Microcephaly autosomal dominant,Paroxysmal familial ventricular fibrillation,Tobacco Use Disorder,Gilles de la Tourette syndrome,Amyotrophic Lateral Sclerosis
miRNA_location151238488-151238508
miRNA_strand+
miRNA_idMIMAT0004819
miRNA_namehsa-miR-671-3p
miRNA_derived MI0003760
TechniqueFISH
PMID12393800
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