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Gene : FOXL2 Homo sapiens

Name  ? forkhead box L2 Cytological Location  3q22.3
Brief Description  forkhead box L2
Description  This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Expansion of a polyalanine repeat region and other mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq, Jul 2016]
  • synonyms:
  • PINTO,
  • OTTHUMG00000159889,
  • BPES,
  • PFRK,
  • POF3,
  • uc003esw.3,
  • AF301906,
  • BPES1,
  • BPES,
  • NM_023067,
  • BPES1,
  • HGNC:1092,
  • FOXL2
  • identifiers:
  • 668,
  • ENSG00000183770,
  • FOXL2

Genome feature

Region: gene ? Length: 2914  
Location: 3:138944224-138947137 reverse strand Cyto location: 3q22.3

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2 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

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76 SN Ps

5 Cross References

18 Data Sets

8 Homologues

0 Located Features

97 Rna Seq Results