| Primary information |
|---|
| Humcfs Id | Humcfs_997 |
| chromosome_number | chromosome2 |
| name | FRA2L |
| chrlocation | 83300001-90500000 |
| cytoband | 2q22.3 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENST00000409984 |
| gene_name | RETSAT |
| havana_transcript_id | OTTHUMT00000329091 |
| gene_location | 85349432-85354506 |
| gene_orientation | - |
| exon_id | ENSE00001693543, ENSE00001004541, ENSE00001275092, ENSE00001773083 |
| exon_number | 4 |
| gene_description | retinol saturase (all-trans-retinol 13,14-reductase) |
| disease_description | SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1 |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | Karyotyping |
| PMID | 2254969 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |