FOXD4

From Wikipedia, the free encyclopedia


Forkhead box D4
Identifiers
Symbol(s) FOXD4; FKHL9; FOXD4A; FREAC5; MGC105106
External IDs OMIM: 601092
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 2298 n/a
Ensembl ENSG00000184492 n/a
Uniprot Q12950 n/a
Refseq NM_207305 (mRNA)
NP_997188 (protein)
n/a (mRNA)
n/a (protein)
Location Chr 9: 0.11 - 0.11 Mb n/a
Pubmed search [1] n/a

Forkhead box D4, also known as FOXD4, is a human gene.[1]


[edit] References

[edit] Further reading

  • Pierrou S, Hellqvist M, Samuelsson L, et al. (1994). "Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending.". EMBO J. 13 (20): 5002–12. PMID 7957066. 
  • Larsson C, Hellqvist M, Pierrou S, et al. (1997). "Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12).". Genomics 30 (3): 464–9. doi:10.1006/geno.1995.1266. PMID 8825632. 
  • Cederberg A, Betz R, Lagercrantz S, et al. (1997). "Chromosome localization, sequence analysis, and expression pattern identify FKHL 18 as a novel human forkhead gene.". Genomics 44 (3): 344–6. doi:10.1006/geno.1997.4864. PMID 9325056. 
  • Freyaldenhoven BS, Fried C, Wielckens K (2003). "FOXD4a and FOXD4b, two new winged helix transcription factors, are expressed in human leukemia cell lines.". Gene 294 (1-2): 131–140. PMID 12234674. 
  • Fan Y, Newman T, Linardopoulou E, Trask BJ (2003). "Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regions.". Genome Res. 12 (11): 1663–72. doi:10.1101/gr.338402. PMID 12421752. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932. 
  • Humphray SJ, Oliver K, Hunt AR, et al. (2004). "DNA sequence and analysis of human chromosome 9.". Nature 429 (6990): 369–74. doi:10.1038/nature02465. PMID 15164053. 
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334. 
  • Minoretti P, Arra M, Emanuele E, et al. (2007). "A W148R mutation in the human FOXD4 gene segregating with dilated cardiomyopathy, obsessive-compulsive disorder, and suicidality.". Int. J. Mol. Med. 19 (3): 369–72. PMID 17273782.