Detailed description page of humcfs

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ACVR1B details
Primary information
gene_nameACVR1B
Humcfs IdHumcfs_3393
chromosome_numberchromosome12
nameFRA12A
chrlocation46400001-54900000
cytoband12q13.1
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000135503
havana_transcript_idOTTHUMT00000397003
gene_location51951706-51976364
gene_orientation+
exon_idENSE00002213093, ENSE00002229115, ENSE00003670861, ENSE00002286002
exon_number4
gene_descriptionactivin A receptor, type IB
disease_descriptionPheochromocytoma,Thyroid carcinoma,Neoplasms, Second Primary,aggressive cancer,Malignant neoplasm of thyroid,hearing impairment,Schizophrenia,Myocardial Ischemia,Tobacco Use Disorder,Pancreatic carcinoma,Pituitary Neoplasms,Tumor Angiogenesis,Hearing Loss, Partial,Neoplasm Recurrence, Local,Malignant neoplasm of pancreas,Breast Carcinoma,Head and Neck Neoplasms
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID8833161
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