IRF8
From SNPedia
is a | gene |
is | mentioned by |
Full name | interferon regulatory factor 8 |
EntrezGene | 3394 |
PheGenI | 3394 |
VariationViewer | 3394 |
ClinVar | IRF8 |
GeneCards | IRF8 |
dbSNP | 3394 |
Diseases | IRF8 |
SADR | 3394 |
HugeNav | 3394 |
wikipedia | IRF8 |
IRF8 | |
gopubmed | IRF8 |
EVS | IRF8 |
HEFalMp | IRF8 |
MyGene2 | IRF8 |
23andMe | IRF8 |
UniProt | Q02556 |
Ensembl | ENSG00000140968 |
OMIM | 601565 |
# SNPs | 12 |
Max Magnitude | Chromosome position | Summary | |
---|---|---|---|
rs1044873 | 0 | 85,922,065 | |
rs10514610 | 0 | 85,908,569 | |
rs11117415 | 0 | 85,917,080 | |
rs144424711 | 0 | 85,918,417 | |
rs391525 | 0 | 85,910,833 | |
rs397514710 | 0 | 85,909,137 | |
rs397514711 | 0 | 85,909,053 | |
rs424971 | 0 | 85,912,844 | |
rs774835569 | 0 | 85,918,486 | |
rs8046526 | 0 | 85,918,029 | |
rs886039596 | 0 | 85,903,024 | |
rs925994 | 0 | 85,912,411 |
IRF8, Interferon regulatory factor 8 or interferon consensus sequence-binding protein, is a transcription factor involved in cell maturation.
rs11642873 is associated at GWAS level with systemic sclerosis.
rs397514711 causes human dendritic-cell immunodeficiency.