| Primary information |
|---|
| Humcfs Id | Humcfs_4769 |
| chromosome_number | chromosome19 |
| name | FRA19B |
| chrlocation | 1-20000000 |
| cytoband | 19p13 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000130477 |
| gene_name | UNC13A |
| havana_transcript_id | OTTHUMT00000376171 |
| gene_location | 17605321-17688349 |
| gene_orientation | - |
| exon_id | ENSE00002357678, ENSE00003574637, ENSE00003623606, ENSE00002111950, ENSE00003588730, ENSE00003568937, ENSE00001672515, ENSE00001056184, ENSE00001056183, ENSE00001641559, ENSE00000895065, ENSE000009522 |
| exon_number | 45 |
| gene_description | unc-13 homolog A (C. elegans) |
| disease_description | Frontotemporal dementia,Fetal Growth Retardation,Amyotrophic Lateral Sclerosis,Tobacco Use Disorder,Pick Disease of the Brain,Hyperglycemia,Amyotrophic Lateral Sclerosis, Sporadic |
| 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 |