Skip Navigation
National Cancer Institute U.S. National Institutes of Health National Cancer Institute
Genes
  • Gene Tools

Gene Info

Gene Information For:Hs. -, Transcribed locus
Sequence ID:D59942
RefSeqGene ID:NG_009367
Entrez Gene ID:2290
Ensembl ID:ENSG00000176165

Database Links

UniGeneEntrez GeneOMIMEnsembl GeneHPRDVegaSNPSNP: GeneViewSNP: VarViewAssemblies

Gene Expression Data


Associated Diseases (from OMIM)

DiseaseOther Genes
RETT SYNDROME, CONGENITAL VARIANT 

Cytogenetic Location (from UniGene)

Cytogenetic Location:Unknown

Chromosomal Position (from UCSC)

Chromosomal Position:Unknown


Full-Length MGC Clones for This Gene

IMAGE IdStatusAccession GenBank Def Line
5284335Full LengthBC050072forkhead box G1

Protein Infomation

RefSeq
mRNAProteinSwissProtPfam
NM_005249 NP_005240 P55316 Fork_head

Related Sequences

 
mRNAGenPeptSwissProt
BC050072 AAH50072 P55316
X74142 CAA52239 P55316
X74143 CAA52240 P55316
X74144 CAA52241 P55316

Homologs (from HomoloGene)
Note: Both orthologs and paralogs are included.
Organism Symbol Protein Homolog Similarity
(% aa unchanged)
Organism Symbol Entrez
Gene
Gene Info Protein
H.sapiens FOXG1 NP_005240 R.norvegicus Foxg1 24370   NP_036692 98
M.musculus Foxg1 15228 Gene Info NP_032267 97

Gene Ontology
Gene classification by the European Bioinformatics Institute, as recorded in GOA (GO Annotation@EBI)

NCI-Nature Pathway Interaction Database