Detailed description page of humcfs
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ACVR1B details |
Primary information | |
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gene_name | ACVR1B |
Humcfs Id | Humcfs_3393 |
chromosome_number | chromosome12 |
name | FRA12A |
chrlocation | 46400001-54900000 |
cytoband | 12q13.1 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000135503 |
havana_transcript_id | OTTHUMT00000397003 |
gene_location | 51951706-51976364 |
gene_orientation | + |
exon_id | ENSE00002213093, ENSE00002229115, ENSE00003670861, ENSE00002286002 |
exon_number | 4 |
gene_description | activin A receptor, type IB |
disease_description | Pheochromocytoma,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_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | FISH |
PMID | 8833161 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |