Detailed description page of humcfs

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CNTNAP2 details
Primary information
gene_nameCNTNAP2
Humcfs IdHumcfs_2214
chromosome_numberchromosome7
nameFRA7I
chrlocation147900001-159138663
cytoband7q36
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000174469
havana_transcript_idOTTHUMT00000479872
gene_location148133684-148415940
gene_orientation+
exon_idENSE00003761381, ENSE00003761292, ENSE00003770226, ENSE00001379696, ENSE00001390444, ENSE00001379553, ENSE00003486840, ENSE00003679776, ENSE00003773618
exon_number9
gene_descriptioncontactin associated protein-like 2
disease_descriptionSeizures,Attention deficit hyperactivity disorder,Exfoliation Syndrome,Language Delay,Rhabdoid Tumor,Precursor Cell Lymphoblastic Leukemia Lymphoma,NEUROTICISM,Unipolar Depression,Autistic Disorder,AUTISM, SUSCEPTIBILITY TO, 15,Selective mutism specific to childhood and adolescence,Malformations of Cortical Development,Autistic behavior,Neoplasm Metastasis,Speech Delay,Atrial Septal Defects,Dyslexia,Social fear,Cortical Dysplasia-Focal Epilepsy Syndrome,Specific language impairment,Child Development Disorders, Pervasive,Autism Spectrum Disorders,Impaired cognition,nervous system disorder,PITT-HOPKINS SYNDROME,Stuttering,As If Personality,Small cell carcinoma of lung,Cirrhosis,Mental Retardation,Liver Cirrhosis,Language Disorders,Alzheimer's Disease,Adolescent idiopathic scoliosis,Language Development Disorders,Carotid Artery Diseases,Tic, Vocal,Major Depressive Disorder,Isaacs syndrome,Brain Diseases,Cortical Dysplasia,Intellectual Disability,Hepatitis B,Selective Mutism,Obsessive-Comp
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID12393800
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