Misplaced Pages

FOXI3

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Protein-coding gene in the species Homo sapiens
FOXI3
Identifiers
AliasesFOXI3, forkhead box I3
External IDsOMIM: 612351; MGI: 3511278; HomoloGene: 52949; GeneCards: FOXI3; OMA:FOXI3 - orthologs
Gene location (Human)
Chromosome 2 (human)
Chr.Chromosome 2 (human)
Chromosome 2 (human)Genomic location for FOXI3Genomic location for FOXI3
Band2p11.2Start88,446,787 bp
End88,452,693 bp
Gene location (Mouse)
Chromosome 6 (mouse)
Chr.Chromosome 6 (mouse)
Chromosome 6 (mouse)Genomic location for FOXI3Genomic location for FOXI3
Band6|6 C1Start70,933,515 bp
End70,938,050 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • gonad

  • placenta

  • testicle

  • ganglionic eminence

  • anterior pituitary

  • skin of abdomen

  • skin of leg

  • renal cortex
Top expressed in
  • pharyngeal pouch

  • cervical loop

  • stellate reticulum

  • hair follicle

  • salivary gland

  • epiblast

  • inner enamel epithelium

  • surface ectoderm

  • embryo

  • lens
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

344167

232077

Ensembl

ENSG00000214336

ENSMUSG00000055874

UniProt

A8MTJ6

n/a

RefSeq (mRNA)

NM_001135649

NM_001101464

RefSeq (protein)

NP_001129121

n/a

Location (UCSC)Chr 2: 88.45 – 88.45 MbChr 6: 70.93 – 70.94 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Forkead box I3 (FOXI3) is a protein that in humans is encoded by the FOXI3 gene. FOXI3 is a forkhead box transcription factor that is expressed in the development of hair and teeth. One of its mutations is a dominant allele responsible for the heterozygous Hh hairless trait in dogs. It was identified in 2008.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000214336Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000055874Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Drögemüller C, Karlsson EK, Hytönen MK, Perloski M, Dolf G, Sainio K, et al. (September 2008). "A mutation in hairless dogs implicates FOXI3 in ectodermal development". Science. 321 (5895): 1462. Bibcode:2008Sci...321.1462D. doi:10.1126/science.1162525. PMID 18787161. S2CID 206514824.
Transcription factors and intracellular receptors
(1) Basic domains
(1.1) Basic leucine zipper (bZIP)
(1.2) Basic helix-loop-helix (bHLH)
Group A
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)
(2) Zinc finger DNA-binding domains
(2.1) Nuclear receptor (Cys4)
subfamily 1
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
(3) Helix-turn-helix domains
(3.1) Homeodomain
Antennapedia
ANTP class
protoHOX
Hox-like
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
  • transcriptional enhancer factor
(4) β-Scaffold factors with minor groove contacts
(4.1) Rel homology region
(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) Other transcription factors
(0.2) HMGI(Y)
(0.3) Pocket domain
(0.5) AP-2/EREBP-related factors
(0.6) Miscellaneous
see also transcription factor/coregulator deficiencies
Categories: