Primary information |
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gene_name | UNC13A |
Humcfs Id | Humcfs_4769 |
chromosome_number | chromosome19 |
name | FRA19B |
chrlocation | 1-20000000 |
cytoband | 19p13 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000130477 |
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 |