| Primary information |
|---|
| Humcfs Id | Humcfs_4654 |
| chromosome_number | chromosome19 |
| name | FRA19B |
| chrlocation | 1-20000000 |
| cytoband | 19p13 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000064490 |
| gene_name | RFXANK |
| havana_transcript_id | OTTHUMT00000402929 |
| gene_location | 19192911-19201866 |
| gene_orientation | + |
| exon_id | ENSE00002236046, ENSE00003486494, ENSE00003555228, ENSE00003789026, ENSE00003553275, ENSE00001113539, ENSE00003697001, ENSE00003698717 |
| exon_number | 8 |
| gene_description | regulatory factor X-associated ankyrin-containing protein |
| disease_description | Bare Lymphocyte Syndrome, Type II, Complementation Group B,Colorectal Neoplasms,Bare Lymphocyte Syndrome,Combined immunodeficiency,Severe Combined Immunodeficiency,Bare lymphocyte syndrome 2 |
| miRNA_location | 10780263-10780283 |
| miRNA_strand | + |
| miRNA_id | MIMAT0019884 |
| miRNA_name | hsa-miR-4748 |
| miRNA_derived | MI0017387 |
| Technique | FISH |
| PMID | 3568428 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |