Primary information |
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gene_name | RETSAT |
Humcfs Id | Humcfs_997 |
chromosome_number | chromosome2 |
name | FRA2L |
chrlocation | 83300001-90500000 |
cytoband | 2q22.3 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENST00000409984 |
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 |