Detailed description page of humcfs

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FOXP2 details
Primary information
gene_nameFOXP2
Humcfs IdHumcfs_2148
chromosome_numberchromosome7
nameFRA7G
chrlocation 114600001-117400000
cytoband7p31.2
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000128573
havana_transcript_idOTTHUMT00000488574
gene_location114629854-114652253
gene_orientation+
exon_idENSE00003784368, ENSE00003787768, ENSE00003599193, ENSE00003569605, ENSE00003789981
exon_number5
gene_descriptionforkhead box P2
disease_descriptionArticulation Disorders,Bipolar Disorder,Speech impairment,Emotional abuse,Prostate carcinoma,Neurodevelopmental Disorders,Adenoid Cystic Carcinoma,Russell-Silver syndrome,Autistic Disorder,Adult T-Cell Lymphoma/Leukemia,child abuse behavior,Neoplasm Metastasis,Systemic arterial pressure,Schizoaffective Disorder,Malignant neoplasm of breast,Atrial Septal Defects,Breast Carcinoma,Dyslexia,Specific language impairment,Malignant neoplasm of prostate,Mental Depression,Craniofacial Abnormalities,Autism Spectrum Disorders,nervous system disorder,Stuttering,GRN-related frontotemporal dementia,Hallucinations,Frontotemporal Lobar Degeneration,Lymphoma,Cognition Disorders,Diabetes Mellitus, Non-Insulin-Dependent,Inflammatory Bowel Diseases,Language Development Disorders,Major Depressive Disorder,Multiple Myeloma,Speech Disorders,Unipolar Depression,Microcephaly,Communication Disorders, Developmental,Monoclonal Gammopathy of Undetermined Significance,Phobic anxiety disorder,Depressive disorder,Stu
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID10950921
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