FOXI1

GENE INFORMATION

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Gene name

FOXI1 (HGNC Symbol)

Synonyms

FKHL10, FREAC6

Description

Forkhead box I1 (HGNC Symbol)

Entrez gene summary

This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it is possible that this gene plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis. Mutations in this gene may be associated with the common cavity phenotype. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Chromosome

5

Cytoband

q35.1

Chromosome location (bp)

169532901 - 169536727

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000168269 (version 75.37)

Entrez gene

2299

UniProt

Q12951 (UniProt - Evidence at protein level)

neXtProt

NX_Q12951

Antibodypedia

FOXI1 antibodies
 

PROTEIN VIEW

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FOXI1-001
 
FOXI1-002
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

FOXI1-001 ENSP00000304286
ENST00000306268
Q12951
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Show » Show » 378 41 No 0
FOXI1-002 ENSP00000415483
ENST00000449804
Q12951
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Show » Show » 283 30.8 No 0