| Primary information |
|---|
| Humcfs Id | Humcfs_5044 |
| chromosome_number | chromosome19 |
| name | FRA19B |
| chrlocation | 1-20000000 |
| cytoband | 19p13 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000198003 |
| gene_name | CCDC151 |
| havana_transcript_id | OTTHUMT00000458804 |
| gene_location | 11420605-11435782 |
| gene_orientation | - |
| exon_id | ENSE00001117536, ENSE00003553596, ENSE00003668011, ENSE00003613719, ENSE00003676348, ENSE00003591299, ENSE00003655172, ENSE00003630588, ENSE00003592605, ENSE00003501270, ENSE00003525952, ENSE000035816 |
| exon_number | 13 |
| gene_description | coiled-coil domain containing 151 |
| disease_description | Congenital Heart Defects,Kartagener Syndrome,Ciliary Motility Disorders,CILIARY DYSKINESIA, PRIMARY, 30 |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | FISH |
| PMID | 3568428 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |