FOXG1

GENE INFORMATION

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Gene name

FOXG1 (HGNC Symbol)

Synonyms

BF1, FKH2, FKHL1, FKHL2, FKHL3, FKHL4, FOXG1A, FOXG1B, FOXG1C, HBF-3, HFK1, HFK2, HFK3, QIN

Description

Forkhead box G1 (HGNC Symbol)

Entrez gene summary

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]

Chromosome

14

Cytoband

q12

Chromosome location (bp)

29235050 - 29238870

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000176165 (version 75.37)

Entrez gene

2290

UniProt

P55316 (UniProt - Evidence at protein level)

neXtProt

NX_P55316

Antibodypedia

FOXG1 antibodies
 

PROTEIN VIEW

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FOXG1-001
 
FOXG1-201
 
 
 
 
 

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)

FOXG1-001 ENSP00000339004
ENST00000313071
P55316
Show all »
Show » Show » 489 52.4 No 0
FOXG1-201 ENSP00000371975
ENST00000382535
P55316
Show all »
Show » Show » 489 52.4 No 0