| Primary information |
|---|
| gene_name | LIN7B |
| Humcfs Id | Humcfs_4403 |
| chromosome_number | chromosome19 |
| name | FRA19A |
| chrlocation | 32400001-59128983 |
| cytoband | 19q13 |
| type | 5-azacytidine |
| frequency | Common |
| gene_ensembl_id | ENSG00000104863 |
| havana_transcript_id | OTTHUMT00000258981 |
| gene_location | 49114324-49118460 |
| gene_orientation | + |
| exon_id | ENSE00001620869, ENSE00000349030, ENSE00003495515, ENSE00003564202, ENSE00003646225 |
| exon_number | 5 |
| gene_description | lin-7 homolog B (C. elegans) |
| disease_description | Autism Spectrum Disorders,Atrial Septal Defects |
| 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 |