Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (0) GO Terms (11) Nucleotides (91) Proteins (41) Interactants (1) Wiki
XB-GENEPAGE-6257537
???displayGene.symbol???:
 frrs1l

???displayGene.name???: 
ferric-chelate reductase 1-like

???displayGene.synonyms???
cg-6 , cg6 , LOC108719064 ( Nomenclature history )

AI Protein Function :
The frrs1l gene encodes a solute carrier family 52 protein, which is a riboflavin transporter. The protein localizes to the cell membrane and functions in transporting riboflavin (vitamin b2) into cell...[+]



???displayGene.geneInteractants???
Loading ...

Diseases: 


Disease Ontology:
autosomal recessive intellectual developmental disorder

MIM:
DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 37; DEE37

External Links:
Loading gene data...
Please wait while we fetch the latest information
???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


Symbol legend: Blast sequence    View sequence    Literature or expression images   Hover cursor for info