Bos taurus Gene: RFXANK
Summary
InnateDB Gene IDBG-641411.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol RFXANK
Gene Name DNA-binding protein RFXANK
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000001762
Encoded Proteins
DNA-binding protein RFXANK
DNA-binding protein RFXANK
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000064490:
Major histocompatibility (MHC) class II molecules are transmembrane proteins that have a central role in development and control of the immune system. The protein encoded by this gene, along with regulatory factor X-associated protein and regulatory factor-5, forms a complex that binds to the X box motif of certain MHC class II gene promoters and activates their transcription. Once bound to the promoter, this complex associates with the non-DNA-binding factor MHC class II transactivator, which controls the cell type specificity and inducibility of MHC class II gene expression. This protein contains ankyrin repeats involved in protein-protein interactions. Mutations in this gene have been linked to bare lymphocyte syndrome type II, complementation group B. Two transcript variants encoding different isoforms have been described for this gene, with only one isoform showing activation activity. [provided by RefSeq, Jul 2008]
Major histocompatibility (MHC) class II molecules are transmembrane proteins that have a central role in development and control of the immune system. The protein encoded by this gene, along with regulatory factor X-associated protein and regulatory factor-5, forms a complex that binds to the X box motif of certain MHC class II gene promoters and activates their transcription. Once bound to the promoter, this complex associates with the non-DNA-binding factor MHC class II transactivator, which controls the cell type specificity and inducibility of MHC class II gene expression. This protein contains ankyrin repeats involved in protein-protein interactions. Mutations in this gene have been linked to bare lymphocyte syndrome type II, complementation group B. Multiple alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:3986327-3991487
Strand Reverse strand
Band
Transcripts
ENSBTAT00000002309 ENSBTAP00000002309
ENSBTAT00000053592 ENSBTAP00000047746
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 17 interaction(s) predicted by orthology.
Predicted by orthology
Total 17 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0042826 histone deacetylase binding
Biological Process
GO:0007265 Ras protein signal transduction
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0045171 intercellular bridge
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
EGFR1 pathway
REACTOME
KEGG
Antigen processing and presentation pathway
Primary immunodeficiency pathway
Antigen processing and presentation pathway
Primary immunodeficiency pathway
INOH
PID NCI
Signaling events mediated by HDAC Class II
Cross-References
SwissProt
TrEMBL A6QNS0
UniProt Splice Variant
Entrez Gene 100125917
UniGene Bt.74200
RefSeq NM_001105488 XM_005208416 XM_005208417
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC148968 DAAA02019031
GenPept AAI48969
RNA Seq Atlas 100125917