Primary information |
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gene_name | RFXANK |
Humcfs Id | Humcfs_4654 |
chromosome_number | chromosome19 |
name | FRA19B |
chrlocation | 1-20000000 |
cytoband | 19p13 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000064490 |
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 |