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Gene : FOXG1 Homo sapiens

Name  ? forkhead box G1 Cytological Location  14q12
Brief Description  forkhead box G1
Description  This locus encodes a member of the forked-head transcription factor family. The encoded protein, which functions as a repressor, may play a role in brain development. Mutations at this locus have been associated with Rett syndrome. [provided by RefSeq, Feb 2012]
  • synonyms:
  • HBF2,
  • HGNC:3811,
  • HFK1,
  • FKHL4,
  • FOXG1A,
  • HFK3,
  • forkhead box G1C,
  • FOXG1A,
  • FKHL1,
  • FKHL2,
  • BF1,
  • NM_005249,
  • HFK1,
  • forkhead box G1A,
  • HFK3,
  • QIN,
  • uc001wqe.5,
  • brain factor 1,
  • FKHL1,
  • QIN,
  • HBF-1,
  • FKHL3,
  • HBF-G2,
  • BF2,
  • forkhead box G1B,
  • OTTHUMG00000140187,
  • HBF-3,
  • FKHL4,
  • HBF-3,
  • FKH2,
  • FOXG1C,
  • FOXG1B,
  • FKH2,
  • FKHL2,
  • FOXG1C,
  • FOXG1B,
  • HFK2,
  • BF1,
  • HFK2,
  • HBF-2,
  • FHKL3,
  • FOXG1,
  • FKHL3,
  • KHL2
  • identifiers:
  • 2290,
  • ENSG00000176165,
  • FOXG1

Genome feature

Region: gene ? Length: 3491  
Location: 14:28766787-28770277 Cyto location: 14q12


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Proteins

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SNPs

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Disease

1 Diseases

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

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Gene -> HPO annotation (Human Phenotype Ontology)

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Expression

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Other

137 SN Ps

5 Cross References

17 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results