Primary information |
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Humcfs Id | Humcfs_348 |
chromosome_number | chromosome1 |
name | FRA1F |
chrlocation | 142600001-155000000 |
cytoband | 1q21 |
type | Aphidicolin |
frequency | Common |
gene_ensembl_id | ENSG00000143390 |
gene_name | RFX5 |
havana_transcript_id | OTTHUMT00000316354 |
gene_location | 151344792-151346872 |
gene_orientation | - |
exon_id | ENSE00001717317, ENSE00003647996, ENSE00003624294, ENSE00003532823, ENSE00001045114, ENSE00001724780 |
exon_number | 6 |
gene_description | regulatory factor X, 5 (influences HLA class II expression) |
disease_description | Bare Lymphocyte Syndrome, Type II, Complementation Group C,Arteriosclerosis,Bare Lymphocyte Syndrome,Bare Lymphocyte Syndrome, Type II, Complementation Group E,Atherosclerosis,Bare lymphocyte syndrome 2,Congenital chromosomal disease,Major histocompatibility complex class II deficiency,Age related macular degeneration,Colorectal Cancer |
miRNA_location | 153689705-153689793 |
miRNA_strand | - |
miRNA_id | MI0025919 |
miRNA_name | hsa-mir-8083 |
miRNA_derived | NA |
Technique | BAC clones |
PMID | 27625703 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |