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Gene : FOXL1 Homo sapiens

Name  ? forkhead box L1 Cytological Location  16q24.1
Brief Description  forkhead box L1
Description  This gene encodes a member of the forkhead/winged helix-box (FOX) family of transcription factors. FOX transcription factors are characterized by a distinct DNA-binding forkhead domain and play critical roles in the regulation of multiple processes including metabolism, cell proliferation and gene expression during ontogenesis. [provided by RefSeq, Nov 2012]
  • synonyms:
  • FKH6,
  • FREAC7,
  • FOXL1,
  • FREAC7,
  • AF315075,
  • NM_005250,
  • uc002fjr.4,
  • OTTHUMG00000137653,
  • FKHL11,
  • FKHL11,
  • HGNC:3817,
  • FKH6
  • identifiers:
  • 2300,
  • ENSG00000176678,
  • FOXL1

Genome feature

Region: gene ? Length: 4930  
Location: 16:86578549-86583478 Cyto location: 16q24.1


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Gene --> Orthologues

Interactions

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Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

415 SN Ps

5 Cross References

15 Data Sets

38 Homologues

0 Located Features

97 Rna Seq Results