Detailed description page of humcfs
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SCN1B details |
| Primary information | |
|---|---|
| gene_name | SCN1B |
| Humcfs Id | Humcfs_4179 |
| chromosome_number | chromosome19 |
| name | FRA19A |
| chrlocation | 32400001-59128983 |
| cytoband | 19q13 |
| type | 5-azacytidine |
| frequency | Common |
| gene_ensembl_id | ENSG00000105711 |
| havana_transcript_id | OTTHUMT00000461568 |
| gene_location | 35030733-35040073 |
| gene_orientation | + |
| exon_id | ENSE00003059059, ENSE00003557397, ENSE00002981763, ENSE00001254304, ENSE00000862735, ENSE00003150708 |
| exon_number | 6 |
| gene_description | sodium channel, voltage gated, type I beta subunit |
| disease_description | Seizures,Sudden infant death syndrome,Familial benign neonatal epilepsy,Neoplasm Metastasis,ATRIAL FIBRILLATION, FAMILIAL, 13,Brugada Syndrome (disorder),Malignant neoplasm of breast,Breast Carcinoma,Absence Epilepsy,Long QT Syndrome,Infantile Severe Myoclonic Epilepsy,Diabetes Mellitus, Non-Insulin-Dependent,Atrial Fibrillation,Generalized Epilepsy with Febrile Seizures Plus,CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder),Brugada Syndrome 5,Epilepsy, Generalized,Epilepsy,Epilepsy, Temporal Lobe,GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1,Febrile Convulsions,Epilepsies, Myoclonic |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | Karyotyping |
| PMID | 2579891 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |