FOXF1
Identifiers
FOXF1, ACDMPV, FKHL5, FREAC1, forkhead box F1
External IDs
OMIM: 601089; MGI: 1347470; HomoloGene: 1114; GeneCards: FOXF1; OMA:FOXF1 - orthologs
Gene location (Human)
16q24.1
Start
End
Gene location (Mouse)
Chromosome 8 (mouse)[2]
8 E1|8 70.31 cM
Start
End
Cellular component
Biological process
Mouse
RefSeq (mRNA)
RefSeq (protein)
Location (UCSC)
PubMed search
Forkhead box protein F1 (FOXF1) is a protein that in humans is encoded by the FOXF1 gene.[5][6][7]
This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. FOX1 protein is important in the development of the pulmonary mesenchyme and the development of the gastrointestinal tract.[8]
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
(1.2) Basic helix-loop-helix (bHLH)
Group B
Group C
bHLH-PAS
Group D
Group E
Group F
bHLH-COE
(1.3) bHLH-ZIP
(1.4) NF-1
(1.5) RF-X
(1.6) Basic helix-span-helix (bHSH)
subfamily 2
subfamily 3
subfamily 4
subfamily 5
subfamily 6
subfamily 0
(2.2) Other Cys4
(2.3) Cys2His2
(2.4) Cys6
(2.5) Alternating composition
(2.6) WRKY
metaHOX
NK-like
other
(3.2) Paired box
(3.3) Fork head / winged helix
(3.4) Heat shock factors
(3.5) Tryptophan clusters
(3.6) TEA domain
(4.2) STAT
(4.3) p53-like
(4.4) MADS box
(4.6) TATA-binding proteins
(4.7) High-mobility group
(4.9) Grainyhead
(4.10) Cold-shock domain
(4.11) Runt
(0.3) Pocket domain
(0.6) Miscellaneous