2. Gene
  3. Foxl1 - forkhead box L1 Gene

Foxl1 - forkhead box L1 Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Mus musculus

Also known as Fkh6; fkh-6; FREAC7

Gene ID: 14241 | Gene type: protein coding

About Foxl1

Summary

Enables DNA-binding transcription factor activity. Acts upstream of or within several processes, including Peyer's patch morphogenesis; proteoglycan biosynthetic process; and visceral mesoderm-endoderm interaction involved in midgut development. Predicted to be located in nucleus. Is expressed in several structures, including alimentary system; central nervous system; heart; sensory organ; and urinary system. Orthologous to human FOXL1 (forkhead box L1). [provided by Alliance of Genome Resources, Apr 2022]

Foxl1 Products(1)

mRNA Protein Name
NM_008024.3 NP_032050.2 forkhead box protein L1
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
19049965 MGI
Biological Process GO Annotation Evidence Reference Source
acts upstream of or within Peyer's patch morphogenesis IMP
IMP: Inferred from mutant phenotype
12648490 MGI
acts upstream of or within proteoglycan biosynthetic process IMP
IMP: Inferred from mutant phenotype
11555641 MGI
acts upstream of or within regulation of Wnt signaling pathway IMP
IMP: Inferred from mutant phenotype
11555641 MGI
acts upstream of or within visceral mesoderm-endoderm interaction involved in midgut development IMP
IMP: Inferred from mutant phenotype
9203584 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

forkhead box protein L1

forkhead homolog 6

forkhead-related protein FKHL11

transcription factor FKH-6

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS05061 FOXL1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Foxl1 NCBI NCBI:2300